Item | Value |
---|---|
geneid | 1003 |
ensemblid | ENSG00000179776.20 |
hgncid | 1764 |
symbol | CDH5 |
name | cadherin 5 |
refseq_nuc | NM_001795.5 |
refseq_prot | NP_001786.2 |
ensembl_nuc | ENST00000341529.8 |
ensembl_prot | ENSP00000344115.3 |
mane_status | MANE Select |
chr | chr16 |
start | 66366691 |
end | 66404784 |
strand | + |
ver | v1.2 |
region | chr16:66366691-66404784 |
region5000 | chr16:66361691-66409784 |
regionname0 | CDH5_chr16_66366691_66404784 |
regionname5000 | CDH5_chr16_66361691_66409784 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 784 | 304 | 75 | 53 | 139 | 9 | 27 | 105 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0002 | 1/0 | 784 | 83 | 13 | 18 | 28 | 5 | 18 | 22 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0003 | 0/0 | 784 | 8 | 0 | 4 | 0 | 2 | 2 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0004 | 0/0 | 784 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0005 | 0/0 | 784 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0006 | 0/0 | 784 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0007 | 0/0 | 784 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0008 | 0/0 | 784 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0009 | 0/0 | 784 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0010 | 0/0 | 784 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
a0011 | 0/0 | 784 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | MQRLM others(779): Show |
chr16 | 66361691 | 66409784 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2352 | 150 | 29 | 25 | 86 | 5 | 5 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0002 | 0/1 | 2352 | 108 | 27 | 14 | 50 | 1 | 15 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0004 | 0/0 | 2352 | 30 | 9 | 13 | 1 | 3 | 4 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0005 | 0/0 | 2352 | 9 | 8 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0007 | 0/0 | 2352 | 3 | 0 | 0 | 0 | 0 | 3 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0009 | 0/0 | 2352 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0010 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0001c0019 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0002c0003 | 1/0 | 2352 | 81 | 12 | 18 | 27 | 5 | 18 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0002c0013 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0002c0018 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0003c0006 | 0/0 | 2352 | 8 | 0 | 4 | 0 | 2 | 2 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0004c0008 | 0/0 | 2352 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0005c0020 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0006c0016 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0007c0014 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0008c0015 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0009c0011 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0010c0017 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 | ||
a0011c0012 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ATGCA others(2347): Show |
chr16 | 66361691 | 66409784 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4057 | 139 | 26 | 23 | 82 | 4 | 4 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0002 | 0/0 | 4057 | 3 | 0 | 0 | 1 | 1 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0007 | 0/0 | 4057 | 2 | 2 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0008 | 0/0 | 4057 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0013 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0017 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0019 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0001t0020 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0001 | 0/1 | 4057 | 92 | 16 | 13 | 48 | 1 | 13 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0002 | 0/0 | 4057 | 4 | 4 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0006 | 0/0 | 4057 | 4 | 4 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0009 | 0/0 | 4057 | 2 | 0 | 0 | 1 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0012 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0016 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0018 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0021 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0022 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0002t0023 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0004t0001 | 0/0 | 4057 | 25 | 8 | 10 | 1 | 2 | 4 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0004t0004 | 0/0 | 4057 | 4 | 1 | 2 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0004t0010 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0005t0001 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0005t0002 | 0/0 | 4057 | 3 | 3 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0005t0003 | 0/0 | 4057 | 5 | 5 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0007t0002 | 0/0 | 4057 | 2 | 0 | 0 | 0 | 0 | 2 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0007t0014 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4003): Show |
chr16 | 66361691 | 66409784 |
a0001c0009t0001 | 0/0 | 4057 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0010t0002 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0001c0019t0001 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0003t0001 | 0/0 | 4057 | 3 | 0 | 1 | 1 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0003t0002 | 1/0 | 4057 | 72 | 12 | 16 | 22 | 5 | 16 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0003t0005 | 0/0 | 4057 | 4 | 0 | 0 | 4 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0003t0011 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0003t0015 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0013t0002 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0002c0018t0002 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0003c0006t0001 | 0/0 | 4057 | 8 | 0 | 4 | 0 | 2 | 2 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0004c0008t0002 | 0/0 | 4057 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0005c0020t0001 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0006c0016t0001 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0007c0014t0001 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0008c0015t0001 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0009c0011t0002 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0010c0017t0001 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
a0011c0012t0002 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | ACTCA others(4052): Show |
chr16 | 66361691 | 66409784 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0008g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0017g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0019g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0001t0020g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0009g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0016g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0018g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0021g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0022g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0002t0023g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0004g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0004t0010g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0005t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0007t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0007t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0007t0014g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0009t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0009t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0010t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0001c0019t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0002 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0005g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0011g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0003t0015g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0013t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0002c0018t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0003c0006t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0003c0006t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0003c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0003c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0003c0006t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0003c0006t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0004c0008t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0004c0008t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0005c0020t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0006c0016t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0007c0014t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0008c0015t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0009c0011t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0010c0017t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
a0011c0012t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0310 | EUR | GBR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | GBR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0352 | EUR | FIN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00280 | hp2 | a0002 | c0003 | t0002 | g0002 | EUR | FIN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00323 | hp1 | a0002 | c0003 | t0002 | g0248 | EUR | FIN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00323 | hp2 | a0001 | c0004 | t0001 | g0341 | EUR | FIN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00558 | hp2 | a0002 | c0003 | t0002 | g0253 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00597 | hp1 | a0002 | c0003 | t0002 | g0148 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00609 | hp1 | a0002 | c0003 | t0002 | g0021 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00639 | hp1 | a0002 | c0003 | t0002 | g0266 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00639 | hp2 | a0001 | c0004 | t0001 | g0205 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0354 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | CHS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0245 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00735 | hp1 | a0002 | c0003 | t0002 | g0288 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00735 | hp2 | a0002 | c0003 | t0002 | g0270 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00738 | hp1 | a0001 | c0005 | t0001 | g0291 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00738 | hp2 | a0002 | c0003 | t0002 | g0231 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00741 | hp1 | a0003 | c0006 | t0001 | g0001 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0294 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0210 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0208 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0209 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01074 | hp1 | a0002 | c0003 | t0002 | g0002 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0300 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01099 | hp2 | a0002 | c0003 | t0002 | g0049 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01109 | hp1 | a0005 | c0020 | t0001 | g0060 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01109 | hp2 | a0002 | c0003 | t0002 | g0244 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01167 | hp2 | a0001 | c0004 | t0001 | g0019 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01168 | hp1 | a0001 | c0001 | t0008 | g0025 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01168 | hp2 | a0003 | c0006 | t0001 | g0216 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0025 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0265 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01192 | hp1 | a0002 | c0003 | t0011 | g0295 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01192 | hp2 | a0002 | c0003 | t0002 | g0002 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01243 | hp2 | a0001 | c0004 | t0001 | g0207 | AMR | PUR | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01255 | hp2 | a0002 | c0003 | t0002 | g0225 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01256 | hp2 | a0001 | c0004 | t0004 | g0004 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01257 | hp1 | a0006 | c0016 | t0001 | g0304 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0343 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0138 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01358 | hp2 | a0003 | c0006 | t0001 | g0001 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01361 | hp1 | a0002 | c0003 | t0002 | g0362 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01433 | hp2 | a0003 | c0006 | t0001 | g0024 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01515 | hp1 | a0003 | c0006 | t0001 | g0001 | EUR | IBS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01515 | hp2 | a0002 | c0003 | t0002 | g0002 | EUR | IBS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01516 | hp1 | a0002 | c0003 | t0002 | g0002 | EUR | IBS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01891 | hp1 | a0001 | c0005 | t0002 | g0217 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01934 | hp1 | a0001 | c0004 | t0004 | g0004 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01934 | hp2 | a0001 | c0004 | t0001 | g0019 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01981 | hp2 | a0001 | c0002 | t0022 | g0175 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02004 | hp2 | a0007 | c0014 | t0001 | g0100 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0296 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0183 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02148 | hp2 | a0002 | c0003 | t0002 | g0359 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02165 | hp1 | a0002 | c0003 | t0002 | g0325 | EAS | CDX | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CDX | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02280 | hp1 | a0002 | c0003 | t0002 | g0357 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02280 | hp2 | a0002 | c0003 | t0002 | g0121 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02451 | hp2 | a0001 | c0005 | t0002 | g0056 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02572 | hp1 | a0002 | c0003 | t0002 | g0238 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02572 | hp2 | a0002 | c0003 | t0002 | g0118 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02602 | hp2 | a0002 | c0003 | t0015 | g0298 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0055 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0189 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0239 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02647 | hp2 | a0001 | c0019 | t0001 | g0042 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02683 | hp1 | a0002 | c0003 | t0002 | g0313 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02683 | hp2 | a0003 | c0006 | t0001 | g0172 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0054 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02698 | hp2 | a0002 | c0003 | t0002 | g0267 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02717 | hp2 | a0002 | c0003 | t0002 | g0240 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02738 | hp2 | a0001 | c0007 | t0002 | g0196 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0082 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02818 | hp2 | a0002 | c0018 | t0002 | g0135 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0096 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02886 | hp2 | a0001 | c0002 | t0023 | g0119 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02895 | hp2 | a0008 | c0015 | t0001 | g0120 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0027 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0027 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0139 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02965 | hp2 | a0001 | c0002 | t0018 | g0058 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02976 | hp2 | a0009 | c0011 | t0002 | g0355 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03017 | hp1 | a0002 | c0003 | t0002 | g0023 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03130 | hp1 | a0001 | c0004 | t0001 | g0206 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0081 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03195 | hp1 | a0002 | c0003 | t0002 | g0356 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03209 | hp1 | a0002 | c0003 | t0002 | g0232 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03209 | hp2 | a0001 | c0005 | t0003 | g0106 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03225 | hp1 | a0001 | c0010 | t0002 | g0039 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03225 | hp2 | a0001 | c0002 | t0021 | g0122 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03239 | hp2 | a0003 | c0006 | t0001 | g0287 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03453 | hp1 | a0001 | c0005 | t0003 | g0107 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03490 | hp1 | a0002 | c0003 | t0002 | g0289 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03491 | hp1 | a0001 | c0004 | t0001 | g0203 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0290 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0204 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | ESN | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03540 | hp1 | a0001 | c0005 | t0003 | g0051 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0117 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03579 | hp2 | a0001 | c0005 | t0003 | g0050 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0293 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03688 | hp1 | a0001 | c0007 | t0002 | g0195 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03704 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03710 | hp2 | a0010 | c0017 | t0001 | g0130 | SAS | PJL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03831 | hp1 | a0001 | c0002 | t0016 | g0264 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03834 | hp1 | a0002 | c0003 | t0002 | g0193 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0282 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03927 | hp1 | a0001 | c0007 | t0014 | g0061 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03927 | hp2 | a0001 | c0002 | t0009 | g0157 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0258 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03942 | hp2 | a0001 | c0004 | t0001 | g0311 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04115 | hp1 | a0002 | c0003 | t0002 | g0301 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04184 | hp1 | a0002 | c0003 | t0002 | g0173 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | BEB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04199 | hp1 | a0002 | c0003 | t0002 | g0142 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04199 | hp2 | a0002 | c0003 | t0002 | g0299 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04204 | hp1 | a0002 | c0003 | t0002 | g0297 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04228 | hp1 | a0002 | c0003 | t0002 | g0242 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0257 | SAS | STU | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | YRI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18612 | hp1 | a0002 | c0003 | t0002 | g0146 | EAS | CHB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | CHB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18747 | hp2 | a0001 | c0004 | t0001 | g0358 | EAS | CHB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18906 | hp1 | a0001 | c0002 | t0006 | g0184 | AFR | YRI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18906 | hp2 | a0002 | c0003 | t0002 | g0233 | AFR | YRI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18939 | hp2 | a0002 | c0003 | t0002 | g0274 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18947 | hp1 | a0002 | c0003 | t0002 | g0273 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18948 | hp1 | a0001 | c0002 | t0009 | g0155 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18954 | hp1 | a0002 | c0003 | t0002 | g0021 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18964 | hp1 | a0002 | c0003 | t0002 | g0147 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18972 | hp2 | a0002 | c0003 | t0002 | g0022 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18974 | hp1 | a0002 | c0003 | t0002 | g0220 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18974 | hp2 | a0002 | c0003 | t0005 | g0005 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18975 | hp1 | a0002 | c0003 | t0001 | g0342 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18978 | hp1 | a0002 | c0003 | t0002 | g0149 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18985 | hp1 | a0002 | c0003 | t0005 | g0005 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18994 | hp1 | a0002 | c0003 | t0002 | g0145 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18994 | hp2 | a0011 | c0012 | t0002 | g0276 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18995 | hp2 | a0002 | c0003 | t0002 | g0022 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18998 | hp1 | a0001 | c0001 | t0019 | g0340 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19000 | hp2 | a0002 | c0003 | t0002 | g0260 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19002 | hp2 | a0004 | c0008 | t0002 | g0363 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19009 | hp1 | a0002 | c0013 | t0002 | g0020 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19009 | hp2 | a0001 | c0001 | t0017 | g0303 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19010 | hp2 | a0004 | c0008 | t0002 | g0364 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19011 | hp2 | a0002 | c0003 | t0005 | g0005 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19012 | hp1 | a0001 | c0009 | t0001 | g0339 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19030 | hp1 | a0001 | c0005 | t0002 | g0353 | AFR | LWK | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | LWK | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | LWK | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19056 | hp1 | a0002 | c0003 | t0002 | g0324 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19057 | hp1 | a0002 | c0003 | t0002 | g0275 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19076 | hp1 | a0002 | c0003 | t0002 | g0150 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19083 | hp1 | a0001 | c0001 | t0020 | g0078 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19084 | hp2 | a0002 | c0003 | t0002 | g0279 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19086 | hp1 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19087 | hp1 | a0001 | c0009 | t0001 | g0338 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19087 | hp2 | a0001 | c0002 | t0012 | g0159 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0023 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20129 | hp1 | a0001 | c0005 | t0003 | g0228 | AFR | ASW | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20129 | hp2 | a0002 | c0003 | t0002 | g0272 | AFR | ASW | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20752 | hp1 | a0002 | c0003 | t0002 | g0247 | EUR | TSI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20752 | hp2 | a0001 | c0004 | t0004 | g0199 | EUR | TSI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20805 | hp2 | a0003 | c0006 | t0001 | g0215 | EUR | TSI | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20905 | hp1 | a0002 | c0003 | t0002 | g0312 | SAS | GIH | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0344 | SAS | GIH | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG01123 | hp2 | a0001 | c0004 | t0010 | g0283 | AMR | CLM | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG02559 | hp2 | a0001 | c0004 | t0001 | g0083 | AFR | ACB | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0080 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
HG03471 | hp2 | a0001 | c0002 | t0006 | g0182 | AFR | MSL | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18955 | hp1 | a0002 | c0003 | t0005 | g0278 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | USA | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | USA | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA21309 | hp1 | a0001 | c0004 | t0004 | g0004 | AFR | LWK | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | LWK | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0201 | REF | REF | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
homoSapiens | grch38p0 | a0002 | c0003 | t0002 | g0277 | REF | REF | CDH5_chr16_66361691_66409784 | CDH5 | chr16 | 66361691 | 66409784 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66389376 | C | T | 1 | a0005 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.635C>T | p.Thr212Met | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/12 | 722/4057 | 635/2355 | 212/784 | chr16 | 66389376 | |||
chr16:66390420 | G | A | 1 | a0007 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.799G>A | p.Val267Met | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/12 | 886/4057 | 799/2355 | 267/784 | chr16 | 66390420 | |||
chr16:66390435 | C | A | 1 | a0009 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.814C>A | p.Arg272Ser | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/12 | 901/4057 | 814/2355 | 272/784 | chr16 | 66390435 | |||
chr16:66390496 | T | G | 1 | a0008 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.875T>G | p.Met292Arg | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/12 | 962/4057 | 875/2355 | 292/784 | chr16 | 66390496 | |||
chr16:66392223 | G | A | 1 | a0006 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1057G>A | p.Ala353Thr | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/12 | 1144/4057 | 1057/2355 | 353/784 | chr16 | 66392223 | |||
chr16:66392241 | G | A | 1 | a0010 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1075G>A | p.Val359Ile | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/12 | 1162/4057 | 1075/2355 | 359/784 | chr16 | 66392241 | |||
chr16:66396070 | G | A | 1 | a0004 | 2 | NA19002.hp2 NA19010.hp2 |
missense_variant | MODERATE | c.1229G>A | p.Arg410His | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/12 | 1316/4057 | 1229/2355 | 410/784 | chr16 | 66396070 | |||
chr16:66398478 | T | C | 1 | a0003 | 8 | HG00741.hp1 HG01168.hp2 HG01358.hp2 others(5): Show |
missense_variant | MODERATE | c.1508T>C | p.Ile503Thr | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/12 | 1595/4057 | 1508/2355 | 503/784 | chr16 | 66398478 | |||
chr16:66398520 | T | C | 7 | a0001 a0003 a0005 others(4): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
missense_variant | MODERATE | c.1550T>C | p.Ile517Thr | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/12 | 1637/4057 | 1550/2355 | 517/784 | chr16 | 66398520 | |||
chr16:66400920 | C | A | 1 | a0011 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.1741C>A | p.Gln581Lys | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/12 | 1828/4057 | 1741/2355 | 581/784 | chr16 | 66400920 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66386982 | C | T | 11 | a0001c0001 a0001c0002 a0001c0009 others(8): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
synonymous_variant | LOW | c.384C>T | p.Gly128Gly | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/12 | 471/4057 | 384/2355 | 128/784 | chr16 | 66386982 | |||
chr16:66388415 | A | G | 1 | a0001c0007 | 3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.591A>G | p.Lys197Lys | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/12 | 678/4057 | 591/2355 | 197/784 | chr16 | 66388415 | |||
chr16:66389464 | G | A | 1 | a0001c0010 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.723G>A | p.Thr241Thr | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/12 | 810/4057 | 723/2355 | 241/784 | chr16 | 66389464 | |||
chr16:66390419 | C | T | 1 | a0001c0019 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.798C>T | p.Val266Val | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/12 | 885/4057 | 798/2355 | 266/784 | chr16 | 66390419 | |||
chr16:66390533 | C | T | 1 | a0002c0013 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.912C>T | p.Asp304Asp | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/12 | 999/4057 | 912/2355 | 304/784 | chr16 | 66390533 | |||
chr16:66398521 | C | T | 10 | a0001c0001 a0001c0005 a0001c0007 others(7): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
synonymous_variant | LOW | c.1551C>T | p.Ile517Ile | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/12 | 1638/4057 | 1551/2355 | 517/784 | chr16 | 66398521 | |||
chr16:66403019 | C | T | 1 | a0001c0009 | 2 | NA19012.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.2205C>T | p.Gly735Gly | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 2292/4057 | 2205/2355 | 735/784 | chr16 | 66403019 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66366697 | G | A | 1 | a0001c0004t0010 | 1 | HG01123.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/12 | 12641 | chr16 | 66366697 | ||||||
chr16:66366711 | G | A | 1 | a0002c0003t0011 | 1 | HG01192.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/12 | 12627 | chr16 | 66366711 | ||||||
chr16:66366712 | G | A | 1 | a0001c0004t0004 | 4 | HG01256.hp2 HG01934.hp1 NA20752.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-66G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/12 | 12626 | chr16 | 66366712 | ||||||
chr16:66366727 | G | A | 1 | a0001c0002t0012 | 1 | NA19087.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/12 | 12611 | chr16 | 66366727 | ||||||
chr16:66403228 | A | T | 28 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0017 others(25): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*59A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 59 | chr16 | 66403228 | ||||||
chr16:66403366 | G | T | 1 | a0001c0002t0009 | 2 | HG03927.hp2 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 197 | chr16 | 66403366 | ||||||
chr16:66403487 | C | A | 1 | a0001c0005t0003 | 5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*318C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 318 | chr16 | 66403487 | ||||||
chr16:66403572 | G | A | 1 | a0001c0001t0007 | 2 | HG02055.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*403G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 403 | chr16 | 66403572 | ||||||
chr16:66403660 | T | C | 1 | a0001c0005t0003 | 5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*491T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 491 | chr16 | 66403660 | ||||||
chr16:66403681 | G | A | 1 | a0001c0002t0016 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 512 | chr16 | 66403681 | ||||||
chr16:66403717 | C | T | 1 | a0001c0002t0023 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 548 | chr16 | 66403717 | ||||||
chr16:66403942 | G | A | 1 | a0001c0001t0017 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*773G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 773 | chr16 | 66403942 | ||||||
chr16:66404090 | G | A | 1 | a0001c0002t0018 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*921G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 921 | chr16 | 66404090 | ||||||
chr16:66404156 | G | T | 1 | a0001c0002t0022 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*987G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 987 | chr16 | 66404156 | ||||||
chr16:66404207 | C | T | 1 | a0001c0002t0006 | 4 | HG02145.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1038C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1038 | chr16 | 66404207 | ||||||
chr16:66404208 | G | A | 1 | a0001c0001t0008 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1039G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1039 | chr16 | 66404208 | ||||||
chr16:66404213 | C | T | 1 | a0001c0005t0003 | 5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1044C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1044 | chr16 | 66404213 | ||||||
chr16:66404340 | G | A | 1 | a0001c0001t0019 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1171G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1171 | chr16 | 66404340 | ||||||
chr16:66404416 | C | T | 1 | a0001c0002t0021 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1247C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1247 | chr16 | 66404416 | ||||||
chr16:66404420 | G | A | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1251 | chr16 | 66404420 | ||||||
chr16:66404597 | CAGGTTGT others(42): Show |
C | 1 | a0001c0007t0014 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430_*1478delGGTT others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1430 | INFO_REALIGN_3_PRIME | chr16 | 66404597 | |||||
chr16:66404607 | T | C | 1 | a0001c0002t0001 | 5 | HG01081.hp1 HG01123.hp1 HG01257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1438T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1438 | chr16 | 66404607 | ||||||
chr16:66404663 | T | G | 1 | a0002c0003t0015 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1494 | chr16 | 66404663 | ||||||
chr16:66404664 | T | C | 1 | a0002c0003t0005 | 4 | NA18955.hp1 NA18974.hp2 NA18985.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1495T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1495 | chr16 | 66404664 | ||||||
chr16:66404697 | G | A | 1 | a0001c0001t0020 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1528G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 12/12 | 1528 | chr16 | 66404697 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66366808 | G | A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-20+50G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66366808 | |||||||
chr16:66366893 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-20+135G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66366893 | |||||||
chr16:66367075 | T | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(220): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-20+317T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66367075 | |||||||
chr16:66367363 | T | G | 8 | a0001c0001t0001g0038 a0001c0002t0001g0007 a0001c0002t0001g0032 others(5): Show |
9 | NA18954.hp2 NA18959.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+605T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66367363 | |||||||
chr16:66367488 | G | A | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-20+730G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66367488 | |||||||
chr16:66368059 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0007g0041 a0001c0019t0001g0042 |
3 | HG00140.hp1 HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-20+1301G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368059 | |||||||
chr16:66368059 | G | C | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-20+1301G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368059 | |||||||
chr16:66368327 | A | G | 2 | a0001c0001t0007g0041 a0001c0019t0001g0042 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-20+1569A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368327 | |||||||
chr16:66368582 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0241 |
2 | NA18988.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-20+1824G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368582 | |||||||
chr16:66368612 | T | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
216 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-20+1854T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368612 | |||||||
chr16:66368634 | C | A | 1 | a0001c0002t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-20+1876C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368634 | |||||||
chr16:66368731 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-20+1973A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368731 | |||||||
chr16:66368874 | A | G | 3 | a0001c0002t0001g0365 a0004c0008t0002g0363 a0004c0008t0002g0364 |
3 | NA18967.hp1 NA19002.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-20+2116A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368874 | |||||||
chr16:66368923 | T | C | 1 | a0002c0003t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-20+2165T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66368923 | |||||||
chr16:66369159 | A | G | 1 | a0002c0003t0002g0362 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-20+2401A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66369159 | |||||||
chr16:66369167 | A | G | 1 | a0002c0003t0002g0220 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20+2409A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66369167 | |||||||
chr16:66369297 | C | T | 23 | a0001c0001t0001g0200 a0001c0001t0001g0211 a0001c0001t0001g0213 others(20): Show |
27 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+2539C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66369297 | |||||||
chr16:66369813 | A | AATCCTCA others(15): Show |
2 | a0001c0002t0002g0223 a0001c0002t0002g0224 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-20+3072_-20+3093d others(24): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66369813 | ||||||
chr16:66369887 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | NA18966.hp1 NA18983.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3129G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66369887 | |||||||
chr16:66369980 | T | TTTTG | 6 | a0001c0001t0001g0249 a0001c0002t0001g0246 a0002c0003t0002g0225 others(3): Show |
6 | HG00323.hp1 HG00733.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3254_-20+3257d others(6): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66369980 | ||||||
chr16:66369980 | TTTTG | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
225 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.-20+3254_-20+3257d others(6): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66369980 | ||||||
chr16:66370035 | T | A | 1 | a0002c0003t0002g0231 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-20+3277T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370035 | |||||||
chr16:66370103 | C | T | 1 | a0001c0002t0002g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+3345C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370103 | |||||||
chr16:66370148 | G | A | 21 | a0001c0001t0001g0200 a0001c0001t0001g0211 a0001c0001t0001g0213 others(18): Show |
25 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20+3390G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370148 | |||||||
chr16:66370220 | G | A | 4 | a0001c0002t0001g0234 a0001c0002t0001g0235 a0002c0003t0002g0232 others(1): Show |
4 | HG02809.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+3462G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370220 | |||||||
chr16:66370252 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-20+3494G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370252 | |||||||
chr16:66370293 | A | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(222): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-20+3535A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370293 | |||||||
chr16:66370294 | C | T | 5 | a0001c0001t0001g0230 a0002c0003t0002g0231 a0002c0003t0002g0238 others(2): Show |
5 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+3536C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370294 | |||||||
chr16:66370351 | A | G | 2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-20+3593A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370351 | |||||||
chr16:66370476 | G | C | 7 | a0001c0001t0001g0040 a0001c0001t0001g0229 a0001c0001t0007g0041 others(4): Show |
7 | HG00140.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+3718G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370476 | |||||||
chr16:66370643 | C | T | 4 | a0002c0003t0002g0231 a0002c0003t0002g0238 a0002c0003t0002g0239 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+3885C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370643 | |||||||
chr16:66370791 | G | A | 1 | a0001c0004t0001g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-20+4033G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66370791 | |||||||
chr16:66371027 | C | G | 1 | a0001c0001t0002g0352 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-20+4269C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371027 | |||||||
chr16:66371159 | C | T | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-20+4401C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371159 | |||||||
chr16:66371167 | C | T | 73 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0169 others(70): Show |
78 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-20+4409C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371167 | |||||||
chr16:66371369 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+4611G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371369 | |||||||
chr16:66371759 | G | T | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-20+5001G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371759 | |||||||
chr16:66371801 | G | A | 1 | a0001c0002t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+5043G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371801 | |||||||
chr16:66371806 | T | C | 6 | a0001c0001t0007g0055 a0001c0002t0002g0057 a0001c0005t0002g0056 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+5048T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371806 | |||||||
chr16:66371826 | C | G | 1 | a0001c0002t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+5068C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371826 | |||||||
chr16:66371832 | GCTGGGTC others(8): Show |
G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
104 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.-20+5077_-20+5091d others(17): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66371832 | ||||||
chr16:66371839 | C | T | 1 | a0001c0002t0001g0010 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-20+5081C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371839 | |||||||
chr16:66371897 | A | G | 11 | a0001c0001t0001g0040 a0001c0001t0001g0230 a0001c0001t0007g0041 others(8): Show |
11 | HG00140.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+5139A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66371897 | |||||||
chr16:66372020 | G | A | 1 | a0001c0001t0007g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+5262G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372020 | |||||||
chr16:66372041 | C | T | 9 | a0001c0002t0001g0007 a0001c0002t0001g0032 a0001c0002t0001g0033 others(6): Show |
10 | HG02809.hp2 HG02896.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+5283C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372041 | |||||||
chr16:66372176 | T | C | 1 | a0001c0002t0001g0252 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-20+5418T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372176 | |||||||
chr16:66372178 | C | T | 1 | a0001c0001t0001g0350 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-20+5420C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372178 | |||||||
chr16:66372200 | A | G | 1 | a0001c0002t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+5442A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372200 | |||||||
chr16:66372495 | G | A | 1 | a0001c0002t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+5737G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372495 | |||||||
chr16:66372566 | G | T | 2 | a0001c0005t0003g0050 a0001c0005t0003g0051 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-20+5808G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372566 | |||||||
chr16:66372679 | G | A | 1 | a0002c0003t0002g0253 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-20+5921G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372679 | |||||||
chr16:66372712 | C | T | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-20+5954C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372712 | |||||||
chr16:66372751 | G | A | 4 | a0001c0001t0001g0230 a0001c0001t0013g0139 a0001c0002t0001g0234 others(1): Show |
4 | HG02809.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+5993G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66372751 | |||||||
chr16:66373037 | C | A | 1 | a0002c0003t0002g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-20+6279C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373037 | |||||||
chr16:66373154 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0013g0139 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-19-6165T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373154 | |||||||
chr16:66373250 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-19-6069G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373250 | |||||||
chr16:66373360 | A | G | 3 | a0001c0001t0001g0351 a0001c0001t0001g0361 a0001c0002t0001g0349 |
3 | HG02129.hp2 NA19007.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-19-5959A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373360 | |||||||
chr16:66373407 | A | AT | 11 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(8): Show |
11 | HG01433.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-5893dupT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66373407 | ||||||
chr16:66373407 | AT | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
185 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-19-5893delT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66373407 | ||||||
chr16:66373407 | ATT | A | 27 | a0001c0001t0001g0059 a0001c0001t0001g0115 a0001c0001t0001g0123 others(24): Show |
27 | HG01109.hp1 HG01255.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-5894_-19-5893d others(4): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66373407 | ||||||
chr16:66373432 | G | A | 13 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0002t0001g0116 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-5887G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373432 | |||||||
chr16:66373501 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-19-5818C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373501 | |||||||
chr16:66373526 | G | A | 12 | a0001c0001t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0198 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19-5793G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373526 | |||||||
chr16:66373541 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0111 others(3): Show |
6 | HG00099.hp1 HG01081.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-5778G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373541 | |||||||
chr16:66373543 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0013g0139 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-19-5776G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373543 | |||||||
chr16:66373683 | A | T | 4 | a0002c0003t0002g0231 a0002c0003t0002g0238 a0002c0003t0002g0239 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5636A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373683 | |||||||
chr16:66373747 | G | T | 1 | a0001c0005t0002g0353 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-5572G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373747 | |||||||
chr16:66373775 | T | C | 5 | a0001c0002t0001g0197 a0002c0003t0002g0231 a0002c0003t0002g0238 others(2): Show |
5 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-5544T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373775 | |||||||
chr16:66373878 | A | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
87 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-19-5441A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373878 | |||||||
chr16:66373878 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-5441A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373878 | |||||||
chr16:66373940 | C | T | 5 | a0001c0002t0001g0197 a0002c0003t0002g0231 a0002c0003t0002g0238 others(2): Show |
5 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-5379C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373940 | |||||||
chr16:66373978 | C | T | 4 | a0002c0003t0002g0231 a0002c0003t0002g0238 a0002c0003t0002g0239 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-5341C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373978 | |||||||
chr16:66373990 | G | C | 82 | a0001c0001t0001g0143 a0001c0001t0001g0169 a0001c0001t0001g0181 others(79): Show |
88 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-19-5329G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66373990 | |||||||
chr16:66374009 | G | A | 1 | a0001c0002t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-5310G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374009 | |||||||
chr16:66374023 | G | A | 1 | a0001c0005t0003g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19-5296G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374023 | |||||||
chr16:66374128 | G | A | 83 | a0001c0001t0001g0143 a0001c0001t0001g0169 a0001c0001t0001g0181 others(80): Show |
90 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.-19-5191G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374128 | |||||||
chr16:66374132 | G | T | 1 | a0002c0003t0001g0344 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19-5187G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374132 | |||||||
chr16:66374188 | G | A | 1 | a0001c0002t0001g0144 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-19-5131G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374188 | |||||||
chr16:66374203 | G | A | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-19-5116G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374203 | |||||||
chr16:66374277 | G | T | 2 | a0001c0005t0003g0106 a0001c0005t0003g0107 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-5042G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374277 | |||||||
chr16:66374397 | C | T | 10 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0185 others(7): Show |
12 | HG02083.hp1 HG02145.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-4922C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374397 | |||||||
chr16:66374404 | C | G | 5 | a0001c0002t0001g0197 a0002c0003t0002g0231 a0002c0003t0002g0238 others(2): Show |
5 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-4915C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374404 | |||||||
chr16:66374413 | G | A | 7 | a0002c0003t0002g0145 a0002c0003t0002g0146 a0002c0003t0002g0147 others(4): Show |
7 | HG00597.hp1 NA18612.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-4906G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374413 | |||||||
chr16:66374423 | C | T | 10 | a0001c0001t0001g0181 a0001c0002t0001g0011 a0001c0002t0001g0133 others(7): Show |
11 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19-4896C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374423 | |||||||
chr16:66374424 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0191 |
2 | HG02258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-19-4895G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374424 | |||||||
chr16:66374441 | C | T | 11 | a0001c0002t0001g0202 a0001c0004t0001g0015 a0001c0004t0001g0203 others(8): Show |
14 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-4878C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374441 | |||||||
chr16:66374527 | C | G | 204 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-19-4792C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374527 | |||||||
chr16:66374566 | G | A | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-19-4753G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374566 | |||||||
chr16:66374654 | T | C | 11 | a0001c0001t0001g0040 a0001c0001t0001g0230 a0001c0001t0007g0041 others(8): Show |
11 | HG00140.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19-4665T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374654 | |||||||
chr16:66374679 | A | G | 13 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0002t0001g0116 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-4640A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374679 | |||||||
chr16:66374691 | CT | C | 9 | a0001c0001t0001g0243 a0001c0001t0001g0259 a0001c0002t0001g0062 others(6): Show |
9 | HG00639.hp1 HG01169.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-4611delT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66374691 | ||||||
chr16:66374791 | T | G | 1 | a0001c0002t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-4528T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374791 | |||||||
chr16:66374860 | C | T | 1 | a0002c0003t0002g0343 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-19-4459C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374860 | |||||||
chr16:66374949 | C | T | 5 | a0001c0001t0001g0143 a0001c0002t0001g0131 a0001c0002t0001g0132 others(2): Show |
5 | HG01255.hp1 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-4370C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66374949 | |||||||
chr16:66375070 | G | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0230 a0001c0001t0007g0041 others(13): Show |
16 | HG00140.hp1 HG00738.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-4249G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375070 | |||||||
chr16:66375111 | G | A | 2 | a0001c0002t0002g0223 a0001c0002t0002g0224 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-19-4208G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375111 | |||||||
chr16:66375140 | C | T | 5 | a0001c0002t0001g0197 a0002c0003t0002g0231 a0002c0003t0002g0238 others(2): Show |
5 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-4179C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375140 | |||||||
chr16:66375186 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-4133C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375186 | |||||||
chr16:66375249 | T | A | 1 | a0001c0002t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-4070T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375249 | |||||||
chr16:66375305 | G | A | 2 | a0001c0005t0003g0106 a0001c0005t0003g0107 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-4014G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375305 | |||||||
chr16:66375318 | C | T | 2 | a0001c0002t0002g0223 a0001c0002t0002g0224 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-19-4001C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375318 | |||||||
chr16:66375501 | T | C | 1 | a0001c0002t0001g0062 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-19-3818T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375501 | |||||||
chr16:66375560 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0013g0139 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-19-3759A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375560 | |||||||
chr16:66375581 | C | T | 7 | a0001c0001t0001g0123 a0001c0002t0001g0198 a0001c0002t0018g0058 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-3738C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375581 | |||||||
chr16:66375750 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-3569G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375750 | |||||||
chr16:66375778 | G | T | 2 | a0001c0001t0007g0041 a0001c0019t0001g0042 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-19-3541G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375778 | |||||||
chr16:66375810 | TA | T | 7 | a0001c0001t0001g0063 a0001c0002t0001g0197 a0001c0004t0001g0208 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-3496delA | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66375810 | ||||||
chr16:66375828 | C | A | 1 | a0002c0003t0002g0267 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-19-3491C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375828 | |||||||
chr16:66375845 | C | T | 121 | a0001c0001t0001g0040 a0001c0001t0001g0115 a0001c0001t0001g0123 others(118): Show |
130 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.-19-3474C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375845 | |||||||
chr16:66375882 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-19-3437G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375882 | |||||||
chr16:66375913 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-3406C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375913 | |||||||
chr16:66375936 | G | A | 121 | a0001c0001t0001g0040 a0001c0001t0001g0115 a0001c0001t0001g0123 others(118): Show |
130 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.-19-3383G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375936 | |||||||
chr16:66375983 | C | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0002t0001g0116 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-3336C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375983 | |||||||
chr16:66375988 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-3331G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66375988 | |||||||
chr16:66376110 | T | TAATA | 3 | a0001c0005t0002g0056 a0002c0003t0002g0313 a0003c0006t0001g0216 |
3 | HG01168.hp2 HG02451.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-19-3182_-19-3179d others(6): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66376110 | ||||||
chr16:66376110 | TAATA | T | 5 | a0001c0001t0001g0040 a0001c0001t0007g0041 a0001c0002t0001g0140 others(2): Show |
5 | HG00140.hp1 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-3182_-19-3179d others(6): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66376110 | ||||||
chr16:66376110 | TAATAAAT others(1): Show |
T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-19-3186_-19-3179d others(10): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66376110 | ||||||
chr16:66376110 | TAATAAAT others(9): Show |
T | 2 | a0001c0002t0002g0223 a0001c0002t0002g0224 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-19-3194_-19-3179d others(18): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 66376110 | ||||||
chr16:66376118 | A | T | 1 | a0002c0003t0002g0150 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-19-3201A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376118 | |||||||
chr16:66376146 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-19-3173A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376146 | |||||||
chr16:66376273 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-19-3046A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376273 | |||||||
chr16:66376292 | C | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | NA18953.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-19-3027C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376292 | |||||||
chr16:66376331 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-19-2988C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376331 | |||||||
chr16:66376381 | G | A | 13 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0109 others(10): Show |
13 | HG00099.hp1 HG01081.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-2938G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376381 | |||||||
chr16:66376491 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-19-2828G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376491 | |||||||
chr16:66376494 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0028 others(37): Show |
44 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.-19-2825C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376494 | |||||||
chr16:66376620 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-19-2699A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376620 | |||||||
chr16:66376678 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-2641T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66376678 | |||||||
chr16:66377009 | G | A | 1 | a0001c0002t0001g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19-2310G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66377009 | |||||||
chr16:66377599 | G | C | 1 | a0010c0017t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19-1720G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66377599 | |||||||
chr16:66377663 | A | G | 85 | a0001c0001t0001g0102 a0001c0001t0001g0143 a0001c0001t0001g0169 others(82): Show |
93 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-19-1656A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66377663 | |||||||
chr16:66377926 | A | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0111 others(4): Show |
7 | HG00099.hp1 HG01081.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-1393A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66377926 | |||||||
chr16:66377962 | C | T | 1 | a0001c0001t0008g0025 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-19-1357C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66377962 | |||||||
chr16:66378002 | C | A | 2 | a0002c0003t0002g0017 a0002c0003t0002g0245 |
3 | HG00733.hp2 HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-19-1317C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378002 | |||||||
chr16:66378011 | T | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
90 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-19-1308T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378011 | |||||||
chr16:66378162 | C | T | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-1157C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378162 | |||||||
chr16:66378180 | C | T | 1 | a0001c0001t0013g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19-1139C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378180 | |||||||
chr16:66378221 | A | G | 204 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-19-1098A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378221 | |||||||
chr16:66378285 | G | A | 1 | a0002c0003t0002g0270 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19-1034G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378285 | |||||||
chr16:66378307 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-19-1012G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378307 | |||||||
chr16:66378318 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0103 a0001c0001t0001g0221 others(2): Show |
5 | HG02723.hp1 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-1001C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378318 | |||||||
chr16:66378662 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-19-657C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378662 | |||||||
chr16:66378753 | G | A | 7 | a0001c0001t0001g0052 a0001c0001t0001g0109 a0001c0001t0001g0111 others(4): Show |
7 | HG00099.hp1 HG01081.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-566G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378753 | |||||||
chr16:66378786 | C | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0002t0001g0116 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-533C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378786 | |||||||
chr16:66378791 | C | G | 13 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0002t0001g0116 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-528C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378791 | |||||||
chr16:66378826 | G | A | 87 | a0001c0001t0001g0102 a0001c0001t0001g0143 a0001c0001t0001g0169 others(84): Show |
95 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-19-493G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378826 | |||||||
chr16:66378891 | C | T | 7 | a0001c0001t0001g0040 a0001c0001t0007g0041 a0001c0002t0001g0140 others(4): Show |
7 | HG00140.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-428C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378891 | |||||||
chr16:66378912 | T | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0002t0001g0198 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-407T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378912 | |||||||
chr16:66378942 | G | A | 1 | a0002c0003t0002g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-377G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66378942 | |||||||
chr16:66379107 | C | T | 20 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0097 others(17): Show |
21 | HG00597.hp2 HG01261.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19-212C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66379107 | |||||||
chr16:66379147 | CG | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.-19-171delG | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66379147 | |||||||
chr16:66379247 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(120): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-19-72T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66379247 | |||||||
chr16:66379292 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-19-27G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 1/11 | chr16 | 66379292 | |||||||
chr16:66379626 | T | A | 1 | a0002c0003t0002g0245 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.210+79T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379626 | |||||||
chr16:66379709 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.210+162G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379709 | |||||||
chr16:66379709 | G | C | 14 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0185 others(11): Show |
14 | HG01891.hp1 HG02145.hp2 HG03471.hp2 others(11): Show |
intron_variant | MODIFIER | c.210+162G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379709 | |||||||
chr16:66379735 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.210+188G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379735 | |||||||
chr16:66379805 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.210+258G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379805 | |||||||
chr16:66379820 | A | G | 351 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(348): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.210+273A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379820 | |||||||
chr16:66379842 | AGGTGGTG others(20): Show |
A | 1 | a0001c0001t0001g0268 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.210+304_210+330del others(27): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379842 | ||||||
chr16:66379883 | A | ATGGTGGT others(83): Show |
1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.210+380_210+381ins others(90): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379883 | ||||||
chr16:66379883 | A | ATGGTGGT others(38): Show |
1 | a0001c0001t0001g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.210+426_210+470dup others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379883 | ||||||
chr16:66379883 | ATGGTGGT others(38): Show |
A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(30): Show |
37 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.210+426_210+470del others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379883 | ||||||
chr16:66379883 | ATGGTGGT others(83): Show |
A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0323 a0001c0002t0001g0282 others(3): Show |
7 | HG00438.hp1 HG00741.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+381_210+470del others(90): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379883 | ||||||
chr16:66379883 | ATGGTGGT others(173): Show |
A | 9 | a0001c0001t0001g0348 a0001c0002t0001g0067 a0001c0002t0001g0198 others(6): Show |
9 | HG02486.hp1 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+381_210+560del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379883 | ||||||
chr16:66379896 | CGGTGATG others(128): Show |
C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(137): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.210+426_210+560del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379896 | ||||||
chr16:66379896 | CGGTGATG others(218): Show |
C | 7 | a0001c0001t0001g0361 a0001c0002t0001g0033 a0001c0002t0001g0132 others(4): Show |
7 | HG01891.hp1 HG02004.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+426_210+650del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379896 | ||||||
chr16:66379928 | T | G | 6 | a0001c0001t0001g0229 a0001c0001t0001g0292 a0001c0002t0001g0257 others(3): Show |
6 | HG02258.hp2 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+381T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379928 | |||||||
chr16:66379928 | T | TTGGTGGT others(38): Show |
1 | a0001c0001t0001g0066 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.210+425_210+426ins others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379928 | ||||||
chr16:66379928 | T | TTGGTGGT others(308): Show |
1 | a0001c0002t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.210+470_210+471ins others(315): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379928 | ||||||
chr16:66379941 | C | CGGTGATG others(38): Show |
19 | a0001c0001t0001g0292 a0001c0005t0001g0291 a0001c0005t0003g0106 others(16): Show |
24 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.210+425_210+426ins others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379941 | ||||||
chr16:66379941 | C | CGGTGATG others(83): Show |
2 | a0002c0003t0002g0225 a0002c0003t0002g0359 |
2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.210+606_210+695dup others(90): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379941 | ||||||
chr16:66379941 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+394C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379941 | |||||||
chr16:66379941 | CGGTGATG others(83): Show |
C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0097 others(15): Show |
19 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.210+606_210+695del others(90): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379941 | ||||||
chr16:66379941 | CGGTGATG others(173): Show |
C | 70 | a0001c0001t0001g0284 a0001c0001t0008g0025 a0001c0002t0001g0007 others(67): Show |
76 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.210+516_210+695del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379941 | ||||||
chr16:66379946 | ATGGTGGT others(176): Show |
A | 1 | a0001c0002t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.210+405_210+587del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379946 | ||||||
chr16:66379973 | T | G | 9 | a0001c0001t0001g0194 a0001c0002t0001g0171 a0001c0002t0001g0218 others(6): Show |
9 | HG01516.hp2 HG01975.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+426T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379973 | |||||||
chr16:66379973 | T | TTGGTGGT others(218): Show |
1 | a0001c0001t0001g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+483_210+484ins others(225): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379973 | ||||||
chr16:66379986 | C | T | 5 | a0001c0002t0001g0171 a0001c0002t0001g0218 a0001c0004t0001g0081 others(2): Show |
5 | HG01975.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+439C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66379986 | |||||||
chr16:66379986 | CGGTGATG others(128): Show |
C | 1 | a0001c0002t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.210+471_210+605del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66379986 | ||||||
chr16:66380018 | G | T | 2 | a0001c0004t0001g0081 a0001c0005t0002g0353 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.210+471G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380018 | |||||||
chr16:66380018 | GTGGTGGT others(128): Show |
G | 5 | a0001c0001t0001g0262 a0001c0001t0001g0302 a0001c0001t0001g0345 others(2): Show |
5 | HG01433.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+484_210+618del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380018 | ||||||
chr16:66380029 | CATGGTGA others(400): Show |
C | 6 | a0002c0003t0002g0027 a0002c0003t0002g0232 a0002c0003t0002g0233 others(3): Show |
7 | HG02280.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+492_210+898del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380029 | ||||||
chr16:66380031 | T | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(35): Show |
43 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.210+484T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380031 | |||||||
chr16:66380031 | T | TGGTGATG others(38): Show |
1 | a0001c0002t0001g0171 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.210+515_210+516ins others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380031 | ||||||
chr16:66380031 | TGGTGATG others(128): Show |
T | 1 | a0001c0002t0001g0258 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.210+516_210+650del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380031 | ||||||
chr16:66380063 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.210+516T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380063 | |||||||
chr16:66380063 | TTGGTGGT others(38): Show |
T | 1 | a0001c0002t0001g0365 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.210+529_210+573del others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380063 | ||||||
chr16:66380076 | C | CGGTGATG others(38): Show |
2 | a0001c0005t0003g0106 a0001c0005t0003g0107 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.210+561_210+605dup others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380076 | ||||||
chr16:66380076 | C | T | 4 | a0001c0001t0001g0229 a0001c0002t0001g0218 a0001c0002t0018g0058 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+529C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380076 | |||||||
chr16:66380076 | CGGTGATG others(128): Show |
C | 1 | a0001c0001t0007g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.210+574_210+708del | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380076 | ||||||
chr16:66380077 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG00408.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.210+530G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380077 | |||||||
chr16:66380077 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.210+530G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380077 | |||||||
chr16:66380097 | AGGGGTAG others(85): Show |
A | 1 | a0002c0003t0002g0150 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.210+553_210+644del others(92): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380097 | ||||||
chr16:66380108 | G | T | 1 | a0001c0002t0002g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.210+561G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380108 | |||||||
chr16:66380121 | T | C | 13 | a0001c0001t0007g0041 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
13 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.210+574T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380121 | |||||||
chr16:66380121 | TGGTGATG others(38): Show |
T | 3 | a0001c0002t0001g0218 a0001c0002t0001g0282 a0003c0006t0001g0287 |
3 | HG03239.hp2 HG03834.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.210+606_210+650del others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380121 | ||||||
chr16:66380153 | T | G | 88 | a0001c0001t0001g0066 a0001c0001t0001g0261 a0001c0001t0001g0284 others(85): Show |
96 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.210+606T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380153 | |||||||
chr16:66380153 | T | TTGGTGGT others(83): Show |
3 | a0001c0004t0001g0117 a0002c0003t0002g0118 a0002c0003t0002g0121 |
3 | HG02280.hp2 HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.210+654_210+743dup others(90): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380153 | ||||||
chr16:66380166 | C | T | 82 | a0001c0001t0001g0066 a0001c0001t0001g0284 a0001c0001t0001g0315 others(79): Show |
89 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.210+619C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380166 | |||||||
chr16:66380166 | CGGTGATG others(38): Show |
C | 2 | a0001c0001t0001g0109 a0001c0005t0002g0353 |
2 | HG02602.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.210+664_210+708del others(45): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380166 | ||||||
chr16:66380211 | T | C | 1 | a0001c0005t0002g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.210+664T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380211 | |||||||
chr16:66380243 | G | T | 5 | a0001c0005t0002g0217 a0002c0003t0002g0293 a0002c0003t0002g0312 others(2): Show |
5 | HG01891.hp1 HG02004.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+696G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380243 | |||||||
chr16:66380257 | G | A | 2 | a0001c0002t0001g0110 a0002c0003t0011g0295 |
2 | HG01192.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.210+710G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380257 | |||||||
chr16:66380274 | T | C | 6 | a0002c0003t0002g0020 a0002c0003t0002g0260 a0002c0003t0002g0273 others(3): Show |
6 | NA18939.hp2 NA18947.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+727T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380274 | |||||||
chr16:66380282 | T | C | 30 | a0001c0001t0007g0041 a0001c0002t0001g0029 a0001c0002t0001g0030 others(27): Show |
30 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.210+735T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380282 | |||||||
chr16:66380285 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0047 |
2 | NA18966.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.210+738G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380285 | |||||||
chr16:66380291 | A | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(278): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.210+744A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380291 | |||||||
chr16:66380428 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0070 others(13): Show |
17 | HG00408.hp1 HG01346.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.210+881G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380428 | |||||||
chr16:66380493 | G | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0256 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.210+946G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380493 | |||||||
chr16:66380501 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(251): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.210+954C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380501 | |||||||
chr16:66380559 | C | G | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.210+1012C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380559 | |||||||
chr16:66380654 | G | A | 1 | a0001c0002t0021g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.210+1107G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380654 | |||||||
chr16:66380702 | T | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(263): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.210+1155T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380702 | |||||||
chr16:66380745 | A | G | 81 | a0001c0001t0001g0315 a0001c0002t0001g0007 a0001c0002t0001g0010 others(78): Show |
88 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.210+1198A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380745 | |||||||
chr16:66380783 | GTGA | G | 6 | a0002c0003t0002g0118 a0002c0003t0002g0121 a0002c0003t0002g0231 others(3): Show |
6 | HG00738.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+1242_210+1244d others(5): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66380783 | ||||||
chr16:66380835 | A | G | 30 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(27): Show |
34 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.210+1288A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380835 | |||||||
chr16:66380865 | T | C | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.210+1318T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380865 | |||||||
chr16:66380868 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.210+1321A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380868 | |||||||
chr16:66380874 | G | C | 1 | a0001c0002t0001g0124 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.210+1327G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66380874 | |||||||
chr16:66381003 | C | T | 22 | a0001c0001t0001g0095 a0001c0002t0001g0029 a0001c0002t0001g0030 others(19): Show |
22 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.210+1456C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381003 | |||||||
chr16:66381036 | A | G | 30 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(27): Show |
34 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.210+1489A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381036 | |||||||
chr16:66381117 | A | C | 2 | a0001c0005t0002g0217 a0001c0005t0002g0353 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.210+1570A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381117 | |||||||
chr16:66381250 | T | A | 2 | a0001c0005t0002g0056 a0001c0010t0002g0039 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.210+1703T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381250 | |||||||
chr16:66381250 | T | C | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.210+1703T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381250 | |||||||
chr16:66381405 | C | T | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.210+1858C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381405 | |||||||
chr16:66381411 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.210+1864C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381411 | |||||||
chr16:66381456 | A | C | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.210+1909A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381456 | |||||||
chr16:66381539 | G | A | 4 | a0002c0003t0002g0231 a0002c0003t0002g0238 a0002c0003t0002g0239 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+1992G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381539 | |||||||
chr16:66381637 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(257): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.210+2090G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381637 | |||||||
chr16:66381647 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.210+2100C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381647 | |||||||
chr16:66381655 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(285): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.210+2108G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381655 | |||||||
chr16:66381735 | C | A | 1 | a0001c0002t0001g0218 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.210+2188C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381735 | |||||||
chr16:66381740 | G | A | 10 | a0002c0003t0001g0354 a0002c0003t0002g0002 a0002c0003t0002g0017 others(7): Show |
15 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.210+2193G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381740 | |||||||
chr16:66381756 | A | C | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.210+2209A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381756 | |||||||
chr16:66381761 | C | T | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.210+2214C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381761 | |||||||
chr16:66381889 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(257): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.210+2342A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66381889 | |||||||
chr16:66382029 | G | A | 2 | a0001c0004t0001g0203 a0001c0004t0001g0204 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.210+2482G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382029 | |||||||
chr16:66382129 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(257): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.210+2582G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382129 | |||||||
chr16:66382136 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(287): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.210+2589C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382136 | |||||||
chr16:66382478 | TGTC | T | 3 | a0002c0003t0002g0022 a0002c0003t0002g0296 a0002c0003t0002g0325 |
4 | HG02027.hp1 HG02165.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+2935_210+2937d others(5): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66382478 | ||||||
chr16:66382489 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.210+2942C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382489 | |||||||
chr16:66382496 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(151): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.210+2949A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382496 | |||||||
chr16:66382579 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(115): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.210+3032G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382579 | |||||||
chr16:66382589 | G | A | 5 | a0001c0002t0001g0067 a0001c0002t0001g0198 a0001c0002t0018g0058 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3042G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382589 | |||||||
chr16:66382717 | C | A | 2 | a0001c0002t0001g0153 a0001c0002t0001g0154 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.210+3170C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382717 | |||||||
chr16:66382744 | A | G | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.210+3197A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382744 | |||||||
chr16:66382872 | G | A | 7 | a0002c0003t0002g0145 a0002c0003t0002g0146 a0002c0003t0002g0147 others(4): Show |
7 | HG00597.hp1 NA18612.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+3325G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382872 | |||||||
chr16:66382954 | C | G | 1 | a0001c0002t0006g0184 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.210+3407C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66382954 | |||||||
chr16:66383177 | G | A | 1 | a0002c0003t0002g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.210+3630G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383177 | |||||||
chr16:66383280 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.211-3529G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383280 | |||||||
chr16:66383294 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.211-3515A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383294 | |||||||
chr16:66383304 | A | C | 1 | a0001c0001t0019g0340 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.211-3505A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383304 | |||||||
chr16:66383329 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.211-3480C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383329 | |||||||
chr16:66383351 | C | G | 1 | a0001c0004t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-3458C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383351 | |||||||
chr16:66383378 | T | C | 3 | a0001c0002t0001g0156 a0001c0002t0009g0155 a0001c0002t0009g0157 |
3 | HG03927.hp2 NA18944.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.211-3431T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383378 | |||||||
chr16:66383867 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.211-2942C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66383867 | |||||||
chr16:66384078 | C | CT | 135 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0053 others(132): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.211-2707dupT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384078 | ||||||
chr16:66384078 | C | CTT | 26 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0036 others(23): Show |
26 | HG01243.hp2 HG01361.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.211-2708_211-2707d others(4): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384078 | ||||||
chr16:66384078 | CTTTTTTT others(6): Show |
C | 1 | a0005c0020t0001g0060 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.211-2719_211-2707d others(15): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384078 | ||||||
chr16:66384146 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211-2663G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384146 | |||||||
chr16:66384171 | G | A | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.211-2638G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384171 | |||||||
chr16:66384253 | AT | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.211-2544delT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384253 | ||||||
chr16:66384335 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(257): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.211-2474C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384335 | |||||||
chr16:66384420 | C | T | 1 | a0002c0003t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.211-2389C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384420 | |||||||
chr16:66384661 | C | CA | 88 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(85): Show |
95 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.211-2128dupA | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384661 | ||||||
chr16:66384661 | C | CAA | 47 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0261 others(44): Show |
51 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.211-2129_211-2128d others(4): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384661 | ||||||
chr16:66384661 | C | CAAA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.211-2130_211-2128d others(5): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384661 | ||||||
chr16:66384692 | G | A | 1 | a0001c0002t0001g0218 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.211-2117G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384692 | |||||||
chr16:66384764 | G | C | 2 | a0001c0005t0002g0056 a0001c0010t0002g0039 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.211-2045G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384764 | |||||||
chr16:66384784 | G | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.211-2025G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384784 | |||||||
chr16:66384901 | G | A | 30 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(27): Show |
34 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.211-1908G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384901 | |||||||
chr16:66384921 | G | A | 77 | a0001c0005t0001g0291 a0001c0005t0002g0217 a0001c0005t0002g0353 others(74): Show |
88 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.211-1888G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66384921 | |||||||
chr16:66384962 | A | AAAAC | 80 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(77): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.211-1831_211-1828d others(6): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66384962 | ||||||
chr16:66385047 | CA | C | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.211-1760delA | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66385047 | ||||||
chr16:66385082 | G | C | 74 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(71): Show |
81 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.211-1727G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66385082 | |||||||
chr16:66385408 | T | C | 2 | a0001c0005t0002g0056 a0001c0010t0002g0039 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.211-1401T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66385408 | |||||||
chr16:66385586 | A | G | 28 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.211-1223A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66385586 | |||||||
chr16:66385765 | A | C | 80 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(77): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.211-1044A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66385765 | |||||||
chr16:66385988 | A | G | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211-821A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66385988 | |||||||
chr16:66386015 | A | C | 29 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(26): Show |
33 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.211-794A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386015 | |||||||
chr16:66386102 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(281): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.211-707A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386102 | |||||||
chr16:66386266 | C | CT | 12 | a0001c0001t0001g0308 a0001c0004t0001g0015 a0001c0004t0001g0080 others(9): Show |
13 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.211-531dupT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 66386266 | ||||||
chr16:66386328 | T | C | 80 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(77): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.211-481T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386328 | |||||||
chr16:66386343 | C | T | 3 | a0001c0002t0006g0183 a0001c0002t0006g0184 a0001c0002t0006g0189 |
3 | HG02145.hp2 HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.211-466C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386343 | |||||||
chr16:66386432 | C | G | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.211-377C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386432 | |||||||
chr16:66386454 | A | C | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.211-355A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386454 | |||||||
chr16:66386601 | C | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(279): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.211-208C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386601 | |||||||
chr16:66386678 | G | C | 8 | a0001c0004t0001g0080 a0001c0004t0001g0081 a0001c0004t0001g0082 others(5): Show |
8 | HG01891.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-131G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 2/11 | chr16 | 66386678 | |||||||
chr16:66387351 | A | G | 1 | a0001c0002t0009g0157 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.499+254A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/11 | chr16 | 66387351 | |||||||
chr16:66387604 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.499+507C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/11 | chr16 | 66387604 | |||||||
chr16:66387820 | G | T | 83 | a0001c0004t0001g0080 a0001c0004t0001g0081 a0001c0004t0001g0082 others(80): Show |
94 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.500-504G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/11 | chr16 | 66387820 | |||||||
chr16:66387852 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0347 |
2 | NA19057.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.500-472C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/11 | chr16 | 66387852 | |||||||
chr16:66387935 | G | A | 21 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0043 others(18): Show |
21 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.500-389G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/11 | chr16 | 66387935 | |||||||
chr16:66388061 | C | G | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.500-263C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 3/11 | chr16 | 66388061 | |||||||
chr16:66388575 | G | A | 3 | a0001c0001t0007g0041 a0001c0001t0007g0055 a0001c0001t0013g0139 |
3 | HG02055.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.616+135G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/11 | chr16 | 66388575 | |||||||
chr16:66388604 | G | A | 5 | a0001c0004t0001g0205 a0001c0004t0001g0209 a0001c0004t0001g0210 others(2): Show |
7 | HG00323.hp2 HG00639.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.616+164G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/11 | chr16 | 66388604 | |||||||
chr16:66388693 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.616+253G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/11 | chr16 | 66388693 | |||||||
chr16:66388866 | G | T | 1 | a0001c0005t0002g0353 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.616+426G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/11 | chr16 | 66388866 | |||||||
chr16:66389141 | G | T | 1 | a0001c0002t0001g0164 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.617-217G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/11 | chr16 | 66389141 | |||||||
chr16:66389166 | A | C | 1 | a0001c0001t0013g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.617-192A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 4/11 | chr16 | 66389166 | |||||||
chr16:66389683 | C | T | 1 | a0002c0003t0002g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.781+161C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/11 | chr16 | 66389683 | |||||||
chr16:66389849 | A | C | 1 | a0002c0003t0002g0240 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.781+327A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/11 | chr16 | 66389849 | |||||||
chr16:66390250 | C | T | 1 | a0001c0002t0001g0188 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.782-153C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/11 | chr16 | 66390250 | |||||||
chr16:66390298 | T | A | 1 | a0005c0020t0001g0060 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.782-105T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/11 | chr16 | 66390298 | |||||||
chr16:66390332 | T | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(117): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.782-71T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 5/11 | chr16 | 66390332 | |||||||
chr16:66390675 | C | A | 1 | a0001c0001t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.969+85C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66390675 | |||||||
chr16:66390830 | G | A | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.969+240G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66390830 | |||||||
chr16:66390847 | C | T | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0043 others(13): Show |
16 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.969+257C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66390847 | |||||||
chr16:66390924 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(245): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.969+334C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66390924 | |||||||
chr16:66390929 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0103 |
3 | HG02622.hp1 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.969+339T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66390929 | |||||||
chr16:66391177 | C | T | 17 | a0001c0005t0001g0291 a0002c0003t0001g0354 a0002c0003t0002g0002 others(14): Show |
22 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.969+587C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391177 | |||||||
chr16:66391205 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.969+615C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391205 | |||||||
chr16:66391233 | G | A | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.969+643G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391233 | |||||||
chr16:66391266 | G | T | 1 | a0001c0002t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.969+676G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391266 | |||||||
chr16:66391273 | C | T | 112 | a0001c0001t0001g0088 a0001c0001t0001g0169 a0001c0001t0001g0181 others(109): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.969+683C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391273 | |||||||
chr16:66391388 | T | G | 1 | a0001c0002t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.970-748T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391388 | |||||||
chr16:66391494 | C | T | 1 | a0001c0002t0001g0179 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.970-642C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391494 | |||||||
chr16:66391630 | G | A | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.970-506G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391630 | |||||||
chr16:66391713 | T | C | 122 | a0001c0002t0001g0007 a0001c0002t0001g0010 a0001c0002t0001g0011 others(119): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.970-423T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391713 | |||||||
chr16:66391783 | G | C | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.970-353G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391783 | |||||||
chr16:66391833 | T | A | 15 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
16 | HG00408.hp1 HG01346.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.970-303T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391833 | |||||||
chr16:66391881 | T | C | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.970-255T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391881 | |||||||
chr16:66391909 | G | A | 1 | a0002c0003t0002g0231 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.970-227G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391909 | |||||||
chr16:66391941 | G | T | 3 | a0001c0002t0001g0218 a0001c0002t0002g0057 a0001c0002t0002g0219 |
3 | NA19030.hp2 NA19043.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.970-195G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391941 | |||||||
chr16:66391959 | C | A | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.970-177C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66391959 | |||||||
chr16:66392006 | G | A | 2 | a0002c0003t0002g0118 a0002c0003t0002g0121 |
2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.970-130G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 6/11 | chr16 | 66392006 | |||||||
chr16:66392423 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1217+40C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392423 | |||||||
chr16:66392461 | G | A | 1 | a0003c0006t0001g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1217+78G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392461 | |||||||
chr16:66392622 | C | T | 2 | a0001c0001t0001g0305 a0001c0002t0021g0122 |
2 | HG01496.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1217+239C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392622 | |||||||
chr16:66392653 | C | G | 1 | a0002c0003t0002g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1217+270C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392653 | |||||||
chr16:66392685 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1217+302G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392685 | |||||||
chr16:66392750 | T | C | 2 | a0001c0001t0007g0041 a0001c0001t0013g0139 |
2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1217+367T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392750 | |||||||
chr16:66392846 | A | T | 11 | a0001c0005t0002g0217 a0001c0005t0002g0353 a0001c0005t0003g0050 others(8): Show |
11 | HG01891.hp1 HG02738.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.1217+463A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392846 | |||||||
chr16:66392933 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1217+550G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66392933 | |||||||
chr16:66393049 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0129 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1217+666T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393049 | |||||||
chr16:66393157 | T | G | 1 | a0001c0001t0013g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1217+774T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393157 | |||||||
chr16:66393192 | G | A | 1 | a0001c0004t0001g0082 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1217+809G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393192 | |||||||
chr16:66393199 | T | C | 18 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(15): Show |
22 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1217+816T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393199 | |||||||
chr16:66393339 | T | G | 5 | a0001c0005t0003g0050 a0001c0005t0003g0051 a0001c0005t0003g0106 others(2): Show |
5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1217+956T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393339 | |||||||
chr16:66393594 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1217+1211C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393594 | |||||||
chr16:66393781 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1217+1398G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393781 | |||||||
chr16:66393865 | T | C | 1 | a0001c0002t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1217+1482T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393865 | |||||||
chr16:66393920 | C | T | 1 | a0001c0004t0001g0096 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1217+1537C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66393920 | |||||||
chr16:66394177 | T | C | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0043 others(13): Show |
16 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1217+1794T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394177 | |||||||
chr16:66394309 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1218-1750C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394309 | |||||||
chr16:66394323 | A | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1218-1736A>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394323 | |||||||
chr16:66394439 | T | C | 1 | a0004c0008t0002g0364 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1218-1620T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394439 | |||||||
chr16:66394554 | A | G | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0043 others(13): Show |
16 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218-1505A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394554 | |||||||
chr16:66394564 | AT | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1218-1485delT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66394564 | ||||||
chr16:66394687 | T | G | 1 | a0001c0002t0001g0032 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1218-1372T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394687 | |||||||
chr16:66394725 | TA | T | 7 | a0001c0005t0002g0217 a0001c0005t0002g0353 a0001c0005t0003g0050 others(4): Show |
7 | HG01891.hp1 HG03209.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-1326delA | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66394725 | ||||||
chr16:66394860 | G | T | 5 | a0001c0005t0003g0050 a0001c0005t0003g0051 a0001c0005t0003g0106 others(2): Show |
5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1218-1199G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394860 | |||||||
chr16:66394865 | G | T | 4 | a0001c0001t0007g0041 a0001c0001t0007g0055 a0001c0001t0013g0139 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-1194G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66394865 | |||||||
chr16:66395018 | C | CT | 23 | a0002c0003t0002g0021 a0002c0003t0002g0027 a0002c0003t0002g0049 others(20): Show |
25 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1218-996dupT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTT | 16 | a0001c0001t0001g0031 a0001c0001t0001g0065 a0001c0001t0001g0066 others(13): Show |
17 | HG00621.hp1 HG02083.hp2 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.1218-997_1218-996d others(4): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTT | 40 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0040 others(37): Show |
43 | HG00140.hp1 HG00597.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1218-998_1218-996d others(5): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(42): Show |
53 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1218-999_1218-996d others(6): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTT | 23 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0070 others(20): Show |
24 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1218-1000_1218-996 others(8): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTT | 8 | a0001c0001t0001g0087 a0001c0001t0001g0111 a0001c0001t0001g0323 others(5): Show |
8 | HG00438.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-1001_1218-996 others(9): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0046 a0001c0001t0001g0134 others(6): Show |
10 | HG01109.hp1 HG01975.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218-1003_1218-996 others(11): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0002t0001g0037 others(5): Show |
8 | HG00408.hp2 HG01070.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218-1004_1218-996 others(12): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(3): Show |
23 | a0001c0001t0001g0074 a0001c0001t0001g0089 a0001c0001t0001g0112 others(20): Show |
24 | HG00609.hp2 HG00642.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1218-1005_1218-996 others(13): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0002t0001g0007 others(7): Show |
11 | HG00673.hp2 HG00733.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1218-1006_1218-996 others(14): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(5): Show |
3 | a0001c0002t0001g0190 a0001c0002t0001g0252 a0001c0002t0006g0184 |
3 | HG02074.hp1 HG04204.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1218-1007_1218-996 others(15): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0006g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1218-1008_1218-996 others(16): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1218-1009_1218-996 others(17): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0001g0010 | 2 | HG00140.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1218-1010_1218-996 others(18): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(10): Show |
1 | a0001c0002t0012g0159 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1218-1012_1218-996 others(20): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | C | CTTTTTTT others(11): Show |
2 | a0001c0002t0001g0168 a0001c0002t0001g0178 |
2 | HG00673.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1218-1013_1218-996 others(21): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTT | C | 8 | a0001c0002t0001g0062 a0001c0002t0001g0067 a0001c0002t0001g0197 others(5): Show |
8 | HG02630.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-997_1218-996d others(4): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0036 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1218-1005_1218-996 others(13): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0137 a0001c0001t0001g0213 a0001c0001t0001g0319 others(1): Show |
4 | HG03490.hp2 HG03491.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-1006_1218-996 others(14): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0038 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
8 | HG02083.hp1 HG03710.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-1007_1218-996 others(15): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0241 a0001c0002t0001g0034 others(3): Show |
8 | NA18954.hp2 NA18955.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218-1008_1218-996 others(16): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0307 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1218-1009_1218-996 others(17): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(8): Show |
C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0169 others(15): Show |
19 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1218-1010_1218-996 others(18): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(9): Show |
C | 28 | a0001c0001t0001g0085 a0001c0001t0001g0243 a0001c0002t0001g0131 others(25): Show |
32 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1218-1011_1218-996 others(19): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0013g0139 a0001c0004t0001g0203 a0001c0005t0002g0217 |
3 | HG01891.hp1 HG02922.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1218-1012_1218-996 others(20): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(11): Show |
C | 7 | a0001c0001t0001g0229 a0001c0001t0001g0332 a0001c0005t0003g0050 others(4): Show |
7 | HG02258.hp2 HG03209.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-1013_1218-996 others(21): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0314 a0001c0007t0002g0196 |
3 | HG02132.hp2 HG02738.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1218-1014_1218-996 others(22): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(13): Show |
C | 14 | a0001c0001t0001g0044 a0001c0001t0001g0308 a0001c0001t0001g0331 others(11): Show |
14 | HG01175.hp2 HG02071.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1218-1015_1218-996 others(23): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0001g0084 a0001c0005t0002g0056 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1218-1016_1218-996 others(24): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(19): Show |
C | 2 | a0001c0002t0001g0032 a0001c0010t0002g0039 |
2 | HG03225.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1218-1021_1218-996 others(29): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395018 | CTTTTTTT others(23): Show |
C | 3 | a0001c0001t0019g0340 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | HG02818.hp1 HG03516.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1218-1025_1218-996 others(33): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395018 | ||||||
chr16:66395031 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1218-1028T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395031 | |||||||
chr16:66395033 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1218-1026T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395033 | |||||||
chr16:66395071 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1218-988C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395071 | |||||||
chr16:66395089 | C | T | 1 | a0002c0003t0002g0359 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1218-970C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395089 | |||||||
chr16:66395385 | CG | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1218-673delG | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395385 | |||||||
chr16:66395395 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1218-664G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395395 | |||||||
chr16:66395501 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1218-558T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395501 | |||||||
chr16:66395503 | C | CT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(58): Show |
69 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1218-535dupT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395503 | ||||||
chr16:66395503 | C | CTT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(192): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1218-536_1218-535d others(4): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395503 | ||||||
chr16:66395503 | C | CTTT | 34 | a0001c0001t0001g0026 a0001c0001t0001g0064 a0001c0001t0001g0069 others(31): Show |
35 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1218-537_1218-535d others(5): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 66395503 | ||||||
chr16:66395607 | T | C | 5 | a0001c0002t0001g0218 a0001c0002t0002g0057 a0001c0002t0002g0219 others(2): Show |
5 | HG02559.hp1 HG02970.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218-452T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395607 | |||||||
chr16:66395736 | A | G | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0043 others(13): Show |
16 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218-323A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395736 | |||||||
chr16:66395793 | C | T | 1 | a0001c0004t0001g0311 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1218-266C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395793 | |||||||
chr16:66395864 | A | T | 1 | a0001c0002t0001g0252 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1218-195A>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 7/11 | chr16 | 66395864 | |||||||
chr16:66396234 | T | G | 15 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
16 | HG00408.hp1 HG01346.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.1360+33T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396234 | |||||||
chr16:66396564 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(273): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1360+363T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396564 | |||||||
chr16:66396606 | GT | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1360+407delT | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 66396606 | ||||||
chr16:66396656 | G | A | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1360+455G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396656 | |||||||
chr16:66396678 | G | A | 5 | a0001c0005t0003g0050 a0001c0005t0003g0051 a0001c0005t0003g0106 others(2): Show |
5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+477G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396678 | |||||||
chr16:66396753 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1360+552G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396753 | |||||||
chr16:66396843 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(273): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1360+642T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396843 | |||||||
chr16:66396854 | T | C | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1360+653T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66396854 | |||||||
chr16:66397014 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0360 |
3 | HG01358.hp1 HG01496.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1360+813C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397014 | |||||||
chr16:66397094 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1361-888G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397094 | |||||||
chr16:66397142 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1361-840T>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397142 | |||||||
chr16:66397365 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1361-617G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397365 | |||||||
chr16:66397433 | G | C | 1 | a0001c0002t0001g0167 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1361-549G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397433 | |||||||
chr16:66397516 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1361-466T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397516 | |||||||
chr16:66397550 | A | G | 16 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0043 others(13): Show |
16 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1361-432A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397550 | |||||||
chr16:66397928 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG01433.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1361-54G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 8/11 | chr16 | 66397928 | |||||||
chr16:66398135 | G | A | 1 | a0002c0003t0002g0313 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1485+29G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 9/11 | chr16 | 66398135 | |||||||
chr16:66398287 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1486-169C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 9/11 | chr16 | 66398287 | |||||||
chr16:66398387 | T | G | 5 | a0002c0003t0001g0354 a0002c0003t0002g0002 a0002c0003t0002g0266 others(2): Show |
9 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.1486-69T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 9/11 | chr16 | 66398387 | |||||||
chr16:66398400 | GACCACCC others(1): Show |
G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(178): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1486-41_1486-34del others(8): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr16 | 66398400 | ||||||
chr16:66398593 | G | A | 7 | a0002c0003t0002g0145 a0002c0003t0002g0146 a0002c0003t0002g0147 others(4): Show |
7 | HG00597.hp1 NA18612.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.1591+32G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66398593 | |||||||
chr16:66398750 | A | G | 18 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0002t0001g0029 others(15): Show |
18 | HG01433.hp1 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1591+189A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66398750 | |||||||
chr16:66398940 | C | A | 1 | a0001c0010t0002g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1591+379C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66398940 | |||||||
chr16:66398950 | G | A | 4 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0180 others(1): Show |
6 | HG02083.hp1 NA18946.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1591+389G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66398950 | |||||||
chr16:66398994 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
177 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1591+433A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66398994 | |||||||
chr16:66399021 | C | G | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1591+460C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66399021 | |||||||
chr16:66399034 | C | T | 1 | a0001c0005t0002g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1591+473C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66399034 | |||||||
chr16:66399345 | T | G | 2 | a0001c0005t0002g0217 a0001c0005t0002g0353 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1591+784T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66399345 | |||||||
chr16:66399674 | C | G | 1 | a0002c0003t0002g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1592-1097C>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66399674 | |||||||
chr16:66399981 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1592-790G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66399981 | |||||||
chr16:66400072 | C | T | 19 | a0001c0004t0001g0015 a0001c0004t0001g0019 a0001c0004t0001g0054 others(16): Show |
23 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1592-699C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400072 | |||||||
chr16:66400188 | G | C | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1592-583G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400188 | |||||||
chr16:66400284 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(272): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1592-487T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400284 | |||||||
chr16:66400377 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(152): Show |
168 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1592-394T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400377 | |||||||
chr16:66400450 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1592-321C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400450 | |||||||
chr16:66400486 | G | A | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1592-285G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400486 | |||||||
chr16:66400600 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1592-171G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400600 | |||||||
chr16:66400608 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1592-163C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400608 | |||||||
chr16:66400668 | G | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(266): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1592-103G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 10/11 | chr16 | 66400668 | |||||||
chr16:66401121 | G | T | 1 | a0002c0003t0002g0343 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1837+105G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401121 | |||||||
chr16:66401264 | C | T | 4 | a0001c0005t0003g0050 a0001c0005t0003g0051 a0001c0005t0003g0106 others(1): Show |
4 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837+248C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401264 | |||||||
chr16:66401292 | A | G | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1837+276A>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401292 | |||||||
chr16:66401492 | T | G | 1 | a0001c0002t0001g0062 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1837+476T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401492 | |||||||
chr16:66401516 | G | A | 1 | a0002c0003t0002g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1837+500G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401516 | |||||||
chr16:66401693 | T | C | 3 | a0001c0007t0002g0195 a0001c0007t0002g0196 a0001c0007t0014g0061 |
3 | HG02738.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1837+677T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401693 | |||||||
chr16:66401744 | C | T | 5 | a0001c0005t0003g0050 a0001c0005t0003g0051 a0001c0005t0003g0106 others(2): Show |
5 | HG03209.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837+728C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401744 | |||||||
chr16:66401768 | C | A | 1 | a0001c0002t0001g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1837+752C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401768 | |||||||
chr16:66401835 | G | A | 1 | a0001c0007t0002g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1838-817G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401835 | |||||||
chr16:66401974 | C | CCCCACTT others(15): Show |
1 | a0001c0001t0001g0113 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1838-676_1838-675i others(24): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 66401974 | ||||||
chr16:66401977 | G | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1838-675G>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66401977 | |||||||
chr16:66402001 | G | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0256 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1838-651G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402001 | |||||||
chr16:66402043 | C | T | 25 | a0001c0002t0001g0218 a0001c0002t0002g0057 a0001c0002t0002g0219 others(22): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1838-609C>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402043 | |||||||
chr16:66402251 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1838-401C>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402251 | |||||||
chr16:66402275 | G | T | 1 | a0001c0002t0001g0158 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1838-377G>T | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402275 | |||||||
chr16:66402416 | CGGGGTGT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(155): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1838-228_1838-222d others(9): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 66402416 | ||||||
chr16:66402468 | GGGATGGG others(24): Show |
G | 2 | a0001c0001t0001g0087 a0001c0001t0017g0303 |
2 | HG02630.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1838-158_1838-128d others(33): Show |
CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 66402468 | ||||||
chr16:66402472 | T | G | 1 | a0001c0002t0001g0187 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1838-180T>G | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402472 | |||||||
chr16:66402557 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(238): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1838-95G>A | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402557 | |||||||
chr16:66402565 | T | C | 3 | a0001c0001t0007g0041 a0001c0001t0007g0055 a0001c0005t0002g0056 |
3 | HG02055.hp1 HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1838-87T>C | CDH5 | ENSG00000179776.20 | transcript | ENST00000341529.8 | protein_coding | 11/11 | chr16 | 66402565 |