Item | Value |
---|---|
geneid | 6051 |
ensemblid | ENSG00000176393.11 |
hgncid | 10078 |
symbol | RNPEP |
name | arginyl aminopeptidase |
refseq_nuc | NM_020216.4 |
refseq_prot | NP_064601.3 |
ensembl_nuc | ENST00000295640.9 |
ensembl_prot | ENSP00000295640.4 |
mane_status | MANE Select |
chr | chr1 |
start | 201982648 |
end | 202006143 |
strand | + |
ver | v1.2 |
region | chr1:201982648-202006143 |
region5000 | chr1:201977648-202011143 |
regionname0 | RNPEP_chr1_201982648_202006143 |
regionname5000 | RNPEP_chr1_201977648_202011143 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 650 | 284 | 75 | 66 | 111 | 7 | 24 | 87 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
a0002 | 0/1 | 650 | 158 | 17 | 15 | 94 | 9 | 22 | 74 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
a0003 | 0/0 | 650 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
a0004 | 0/0 | 650 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
a0005 | 0/0 | 650 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
a0006 | 0/0 | 650 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
a0007 | 0/0 | 650 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | MASGE others(645): Show |
chr1 | 201977648 | 202011143 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1950 | 147 | 17 | 37 | 77 | 4 | 12 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0003 | 0/0 | 1950 | 103 | 37 | 23 | 33 | 3 | 7 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0004 | 0/0 | 1950 | 12 | 2 | 5 | 0 | 0 | 5 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0005 | 0/0 | 1950 | 9 | 9 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0006 | 1/0 | 1950 | 8 | 7 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0012 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0014 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0015 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0017 | 0/0 | 1950 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0001c0019 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0002c0002 | 0/1 | 1950 | 146 | 16 | 15 | 83 | 9 | 22 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0002c0007 | 0/0 | 1950 | 8 | 0 | 0 | 8 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0002c0010 | 0/0 | 1950 | 3 | 0 | 0 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0002c0013 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0003c0009 | 0/0 | 1950 | 4 | 1 | 3 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0004c0008 | 0/0 | 1950 | 4 | 4 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0005c0011 | 0/0 | 1950 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0006c0018 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 | ||
a0007c0016 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | ATGGC others(1945): Show |
chr1 | 201977648 | 202011143 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2399 | 139 | 15 | 37 | 71 | 4 | 12 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0001t0003 | 0/0 | 2399 | 7 | 2 | 0 | 5 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0001t0005 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0003t0001 | 0/0 | 2399 | 102 | 37 | 23 | 32 | 3 | 7 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0003t0002 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
a0001c0004t0001 | 0/0 | 2399 | 12 | 2 | 5 | 0 | 0 | 5 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0005t0001 | 0/0 | 2399 | 9 | 9 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0006t0001 | 1/0 | 2399 | 8 | 7 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0012t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0014t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0015t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0017t0001 | 0/0 | 2399 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0001c0019t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0002c0002t0001 | 0/0 | 2399 | 4 | 3 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0002c0002t0002 | 0/1 | 2395 | 142 | 13 | 15 | 83 | 9 | 21 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
a0002c0007t0002 | 0/0 | 2395 | 6 | 0 | 0 | 6 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
a0002c0007t0004 | 0/0 | 2395 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
a0002c0010t0002 | 0/0 | 2395 | 3 | 0 | 0 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
a0002c0013t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0003c0009t0001 | 0/0 | 2399 | 4 | 1 | 3 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0004c0008t0002 | 0/0 | 2395 | 4 | 4 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
a0005c0011t0001 | 0/0 | 2399 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0006c0018t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2394): Show |
chr1 | 201977648 | 202011143 |
a0007c0016t0002 | 0/0 | 2395 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | GAGCA others(2390): Show |
chr1 | 201977648 | 202011143 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0003 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0005t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0012t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0014t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0015t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0017t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0001c0019t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0002 | 0/0 | 7 | 0 | 1 | 4 | 1 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0289 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0002t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0007t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0010t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0010t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0002c0013t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0003c0009t0001g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0004c0008t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0004c0008t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0004c0008t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0004c0008t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0005c0011t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0006c0018t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
a0007c0016t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0264 | EUR | GBR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0035 | EUR | GBR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0227 | EUR | GBR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0275 | EUR | GBR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0244 | EUR | FIN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0167 | EUR | FIN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0359 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0100 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0124 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0115 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00741 | hp1 | a0003 | c0009 | t0001 | g0012 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0296 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01081 | hp1 | a0001 | c0004 | t0001 | g0136 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0106 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0175 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01175 | hp2 | a0003 | c0009 | t0001 | g0012 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0360 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01255 | hp1 | a0003 | c0009 | t0001 | g0012 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01261 | hp2 | a0001 | c0017 | t0001 | g0001 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01361 | hp1 | a0001 | c0004 | t0001 | g0141 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0197 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0249 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0196 | EUR | IBS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0274 | EUR | IBS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0235 | EUR | IBS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0202 | EUR | IBS | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0278 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01884 | hp2 | a0004 | c0008 | t0002 | g0104 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0288 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0127 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01943 | hp1 | a0001 | c0004 | t0001 | g0138 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0248 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0083 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0356 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0142 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0295 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02027 | hp2 | a0002 | c0007 | t0004 | g0348 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0090 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02080 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02083 | hp1 | a0001 | c0015 | t0001 | g0042 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0331 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02145 | hp1 | a0001 | c0006 | t0001 | g0204 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0228 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | CDX | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02258 | hp1 | a0001 | c0006 | t0001 | g0232 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0209 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02280 | hp1 | a0001 | c0006 | t0001 | g0281 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0286 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0129 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02523 | hp1 | a0002 | c0007 | t0004 | g0302 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0283 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0099 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02622 | hp1 | a0006 | c0018 | t0001 | g0220 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0180 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02630 | hp1 | a0001 | c0006 | t0001 | g0183 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0361 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0297 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0277 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02723 | hp1 | a0004 | c0008 | t0002 | g0284 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0206 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02735 | hp2 | a0001 | c0004 | t0001 | g0135 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02738 | hp2 | a0001 | c0004 | t0001 | g0210 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02809 | hp2 | a0001 | c0005 | t0001 | g0059 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0061 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02897 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02970 | hp1 | a0005 | c0011 | t0001 | g0033 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0218 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02976 | hp2 | a0001 | c0006 | t0001 | g0276 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0212 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0231 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03098 | hp1 | a0004 | c0008 | t0002 | g0353 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0184 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0355 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03139 | hp2 | a0004 | c0008 | t0002 | g0354 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0349 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03239 | hp2 | a0001 | c0004 | t0001 | g0130 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0056 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0285 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0287 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03516 | hp2 | a0002 | c0013 | t0001 | g0062 | AFR | ESN | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03579 | hp1 | a0005 | c0011 | t0001 | g0033 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03654 | hp1 | a0001 | c0004 | t0001 | g0291 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0080 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0335 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0139 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0199 | SAS | PJL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0282 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0344 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0205 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0270 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0290 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0342 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0198 | SAS | BEB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0236 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0253 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0271 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0207 | SAS | STU | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0292 | AFR | YRI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18522 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | YRI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | CHB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | CHB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0055 | AFR | YRI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18906 | hp2 | a0001 | c0014 | t0001 | g0058 | AFR | YRI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0346 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18952 | hp1 | a0002 | c0007 | t0002 | g0046 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0326 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18970 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18991 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18992 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0318 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19030 | hp1 | a0001 | c0012 | t0001 | g0057 | AFR | LWK | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | LWK | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | LWK | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19054 | hp1 | a0002 | c0007 | t0002 | g0347 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19056 | hp2 | a0002 | c0010 | t0002 | g0021 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19057 | hp1 | a0002 | c0010 | t0002 | g0021 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19059 | hp2 | a0007 | c0016 | t0002 | g0233 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19060 | hp1 | a0002 | c0007 | t0002 | g0045 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19063 | hp1 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19063 | hp2 | a0002 | c0007 | t0002 | g0045 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19067 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19072 | hp2 | a0002 | c0010 | t0002 | g0333 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19077 | hp2 | a0001 | c0003 | t0002 | g0092 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19088 | hp1 | a0002 | c0007 | t0002 | g0021 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19090 | hp2 | a0002 | c0007 | t0002 | g0345 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0357 | AFR | YRI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ASW | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20129 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | ASW | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0208 | EUR | TSI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0337 | EUR | TSI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | GIH | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0246 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0060 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG02559 | hp2 | a0001 | c0019 | t0001 | g0350 | AFR | ACB | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0176 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0041 | AFR | MSL | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG06807 | hp1 | a0003 | c0009 | t0001 | g0012 | AFR | USA | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | USA | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | USA | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | USA | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0294 | AFR | LWK | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | LWK | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0289 | REF | REF | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0201 | REF | REF | RNPEP_chr1_201977648_202011143 | RNPEP | chr1 | 201977648 | 202011143 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:201983054 | T | G | 1 | a0005 | 2 | HG02970.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.388T>G | p.Cys130Gly | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/11 | 407/2399 | 388/1953 | 130/650 | chr1 | 201983054 | |||
chr1:201983069 | C | G | 1 | a0006 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.403C>G | p.Arg135Gly | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/11 | 422/2399 | 403/1953 | 135/650 | chr1 | 201983069 | |||
chr1:201996189 | G | T | 1 | a0003 | 4 | HG00741.hp1 HG01175.hp2 HG01255.hp1 others(1): Show |
missense_variant | MODERATE | c.780G>T | p.Lys260Asn | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/11 | 799/2399 | 780/1953 | 260/650 | chr1 | 201996189 | |||
chr1:201997413 | C | T | 1 | a0004 | 4 | HG01884.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.949C>T | p.Arg317Cys | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/11 | 968/2399 | 949/1953 | 317/650 | chr1 | 201997413 | |||
chr1:202001683 | C | G | 1 | a0007 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1342C>G | p.Arg448Gly | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/11 | 1361/2399 | 1342/1953 | 448/650 | chr1 | 202001683 | |||
chr1:202001684 | G | A | 1 | a0007 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1343G>A | p.Arg448Gln | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/11 | 1362/2399 | 1343/1953 | 448/650 | chr1 | 202001684 | |||
chr1:202001687 | G | T | 1 | a0007 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1346G>T | p.Ser449Ile | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/11 | 1365/2399 | 1346/1953 | 449/650 | chr1 | 202001687 | |||
chr1:202001689 | A | T | 1 | a0007 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1348A>T | p.Ile450Phe | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/11 | 1367/2399 | 1348/1953 | 450/650 | chr1 | 202001689 | |||
chr1:202001693 | T | G | 1 | a0007 | 1 | NA19059.hp2 | stop_gained | HIGH | c.1352T>G | p.Leu451* | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/11 | 1371/2399 | 1352/1953 | 451/650 | chr1 | 202001693 | |||
chr1:202004437 | G | A | 3 | a0002 a0004 a0007 |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
missense_variant | MODERATE | c.1735G>A | p.Val579Ile | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/11 | 1754/2399 | 1735/1953 | 579/650 | chr1 | 202004437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:201982756 | C | T | 1 | a0002c0010 | 3 | NA19056.hp2 NA19057.hp1 NA19072.hp2 |
synonymous_variant | LOW | c.90C>T | p.Asn30Asn | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/11 | 109/2399 | 90/1953 | 30/650 | chr1 | 201982756 | |||
chr1:201982846 | C | T | 1 | a0001c0019 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.180C>T | p.Ser60Ser | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/11 | 199/2399 | 180/1953 | 60/650 | chr1 | 201982846 | |||
chr1:201988951 | C | T | 1 | a0001c0017 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.495C>T | p.Phe165Phe | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/11 | 514/2399 | 495/1953 | 165/650 | chr1 | 201988951 | |||
chr1:201989008 | G | A | 4 | a0001c0005 a0001c0012 a0001c0014 others(1): Show |
12 | HG02559.hp1 HG02809.hp2 HG02886.hp2 others(9): Show |
synonymous_variant | LOW | c.552G>A | p.Thr184Thr | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/11 | 571/2399 | 552/1953 | 184/650 | chr1 | 201989008 | |||
chr1:201997358 | A | C | 2 | a0002c0007 a0002c0010 |
11 | HG02027.hp2 HG02523.hp1 NA18952.hp1 others(8): Show |
synonymous_variant | LOW | c.894A>C | p.Gly298Gly | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/11 | 913/2399 | 894/1953 | 298/650 | chr1 | 201997358 | |||
chr1:201999954 | G | A | 5 | a0001c0001 a0001c0012 a0001c0017 others(2): Show |
154 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
synonymous_variant | LOW | c.1143G>A | p.Gln381Gln | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/11 | 1162/2399 | 1143/1953 | 381/650 | chr1 | 201999954 | |||
chr1:202001434 | T | C | 18 | a0001c0001 a0001c0003 a0001c0004 others(15): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
synonymous_variant | LOW | c.1263T>C | p.Val421Val | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 7/11 | 1282/2399 | 1263/1953 | 421/650 | chr1 | 202001434 | |||
chr1:202001692 | T | C | 1 | a0007c0016 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.1351T>C | p.Leu451Leu | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/11 | 1370/2399 | 1351/1953 | 451/650 | chr1 | 202001692 | |||
chr1:202003268 | C | T | 1 | a0001c0015 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1458C>T | p.Pro486Pro | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/11 | 1477/2399 | 1458/1953 | 486/650 | chr1 | 202003268 | |||
chr1:202005584 | G | C | 2 | a0001c0004 a0001c0014 |
13 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(10): Show |
synonymous_variant | LOW | c.1821G>C | p.Leu607Leu | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 11/11 | 1840/2399 | 1821/1953 | 607/650 | chr1 | 202005584 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:202005856 | G | T | 1 | a0001c0001t0005 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 11/11 | 140 | chr1 | 202005856 | ||||||
chr1:202005914 | G | A | 1 | a0002c0007t0004 | 2 | HG02027.hp2 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*198G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 11/11 | 198 | chr1 | 202005914 | ||||||
chr1:202005973 | G | A | 1 | a0001c0001t0003 | 7 | HG02922.hp2 HG03195.hp1 NA18942.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*257G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 11/11 | 257 | chr1 | 202005973 | ||||||
chr1:202006041 | TTCTG | T | 7 | a0001c0003t0002 a0002c0002t0002 a0002c0007t0002 others(4): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*331delTGTC | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 11/11 | 328 | INFO_REALIGN_3_PRIME | chr1 | 202006041 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:201983116 | G | A | 16 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(13): Show |
19 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.447+3G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983116 | |||||||
chr1:201983151 | T | TGCCC | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG01167.hp2 HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.447+39_447+42dupGC others(2): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201983151 | ||||||
chr1:201983166 | C | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.447+53C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983166 | |||||||
chr1:201983182 | T | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.447+69T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983182 | |||||||
chr1:201983196 | CGGGAGGA others(6): Show |
C | 16 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(13): Show |
19 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+91_447+103delG others(12): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201983196 | ||||||
chr1:201983278 | T | C | 1 | a0001c0003t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.447+165T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983278 | |||||||
chr1:201983312 | C | CCTT | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.447+202_447+204dup others(3): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201983312 | ||||||
chr1:201983439 | C | T | 2 | a0002c0002t0002g0047 a0002c0002t0002g0361 |
3 | HG02257.hp2 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.447+326C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983439 | |||||||
chr1:201983446 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.447+333T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983446 | |||||||
chr1:201983470 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(109): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.447+357G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983470 | |||||||
chr1:201983627 | T | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.447+514T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983627 | |||||||
chr1:201983757 | C | T | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.447+644C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983757 | |||||||
chr1:201983766 | T | G | 16 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(13): Show |
19 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+653T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983766 | |||||||
chr1:201983798 | A | G | 9 | a0001c0005t0001g0007 a0001c0005t0001g0055 a0001c0005t0001g0056 others(6): Show |
12 | HG02559.hp1 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.447+685A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983798 | |||||||
chr1:201983810 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(278): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.447+697T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983810 | |||||||
chr1:201983967 | C | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+854C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201983967 | |||||||
chr1:201984007 | T | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+894T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984007 | |||||||
chr1:201984019 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+906G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984019 | |||||||
chr1:201984030 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+917G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984030 | |||||||
chr1:201984041 | G | T | 1 | a0001c0003t0001g0296 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.447+928G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984041 | |||||||
chr1:201984134 | T | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1021T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984134 | |||||||
chr1:201984151 | C | T | 1 | a0001c0003t0001g0360 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.447+1038C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984151 | |||||||
chr1:201984166 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1053G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984166 | |||||||
chr1:201984169 | A | T | 1 | a0001c0003t0001g0295 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.447+1056A>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984169 | |||||||
chr1:201984201 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.447+1088G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984201 | |||||||
chr1:201984212 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1099C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984212 | |||||||
chr1:201984225 | G | T | 1 | a0001c0003t0001g0146 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.447+1112G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984225 | |||||||
chr1:201984252 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.447+1139T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984252 | |||||||
chr1:201984307 | GA | G | 5 | a0001c0003t0001g0217 a0001c0003t0001g0218 a0001c0003t0001g0219 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1198delA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984307 | ||||||
chr1:201984350 | C | T | 29 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(26): Show |
34 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.447+1237C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984350 | |||||||
chr1:201984468 | T | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1355T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984468 | |||||||
chr1:201984501 | C | T | 1 | a0002c0002t0002g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.447+1388C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984501 | |||||||
chr1:201984570 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1457C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984570 | |||||||
chr1:201984613 | TAAC | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1512_447+1514d others(5): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984613 | ||||||
chr1:201984753 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1640T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984753 | |||||||
chr1:201984817 | C | CTTTCTTT others(6): Show |
1 | a0001c0003t0001g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.447+1714_447+1715i others(15): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984817 | ||||||
chr1:201984821 | C | CT | 9 | a0001c0003t0001g0206 a0001c0003t0001g0207 a0001c0003t0001g0208 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.447+1744dupT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | C | CTTTT | 9 | a0001c0003t0001g0216 a0001c0003t0001g0221 a0002c0002t0002g0030 others(6): Show |
11 | HG02040.hp2 HG02056.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.447+1741_447+1744d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | C | CTTTTTTC others(8): Show |
3 | a0002c0002t0001g0068 a0002c0002t0001g0070 a0002c0002t0002g0069 |
3 | HG01168.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.447+1714_447+1715i others(17): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTT | C | 28 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(25): Show |
33 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.447+1741_447+1744d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0293 a0002c0002t0002g0359 |
5 | HG00408.hp1 HG00544.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1734_447+1744d others(13): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTTTTT others(5): Show |
C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.447+1733_447+1744d others(14): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0147 a0001c0001t0001g0174 a0001c0001t0001g0300 others(3): Show |
6 | HG01099.hp2 HG01109.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+1732_447+1744d others(15): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTTTTT others(7): Show |
C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0151 others(25): Show |
35 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.447+1731_447+1744d others(16): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0001g0148 a0001c0003t0001g0149 a0001c0003t0001g0150 |
3 | HG02080.hp1 NA19043.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.447+1730_447+1744d others(17): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984821 | CTTTTTTT others(10): Show |
C | 7 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+1728_447+1744d others(19): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984821 | ||||||
chr1:201984822 | T | TTTTTTCT others(5): Show |
4 | a0001c0001t0001g0023 a0001c0003t0001g0120 a0002c0002t0002g0112 others(1): Show |
4 | HG03453.hp2 NA18968.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1714_447+1715i others(14): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984822 | ||||||
chr1:201984823 | T | TTTTTCTT others(4): Show |
18 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(15): Show |
18 | HG00609.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.447+1714_447+1715i others(13): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984823 | ||||||
chr1:201984824 | T | TTTTCTTT others(3): Show |
34 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0086 others(31): Show |
37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.447+1714_447+1715i others(12): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984824 | ||||||
chr1:201984826 | T | TTC | 8 | a0001c0005t0001g0007 a0001c0005t0001g0055 a0001c0005t0001g0056 others(5): Show |
10 | HG02559.hp1 HG02809.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.447+1714_447+1715i others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201984826 | ||||||
chr1:201984831 | T | C | 2 | a0001c0001t0001g0102 a0001c0003t0001g0099 |
2 | HG02615.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.447+1718T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984831 | |||||||
chr1:201984837 | T | C | 1 | a0001c0003t0001g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.447+1724T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984837 | |||||||
chr1:201984838 | T | C | 28 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(25): Show |
33 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.447+1725T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984838 | |||||||
chr1:201984839 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0293 a0002c0002t0002g0359 |
5 | HG00408.hp1 HG00544.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1726T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984839 | |||||||
chr1:201984840 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.447+1727T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984840 | |||||||
chr1:201984841 | T | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0174 a0001c0001t0001g0300 others(1): Show |
4 | HG01099.hp2 HG01346.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1728T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984841 | |||||||
chr1:201984842 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0151 others(25): Show |
35 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.447+1729T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984842 | |||||||
chr1:201984843 | T | C | 3 | a0001c0001t0001g0148 a0001c0003t0001g0149 a0001c0003t0001g0150 |
3 | HG02080.hp1 NA19043.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.447+1730T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984843 | |||||||
chr1:201984845 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0293 a0001c0003t0001g0048 others(7): Show |
12 | HG00408.hp1 HG00544.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.447+1732T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984845 | |||||||
chr1:201984846 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.447+1733T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984846 | |||||||
chr1:201984847 | T | C | 2 | a0001c0001t0001g0300 a0002c0002t0002g0222 |
2 | HG03831.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.447+1734T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984847 | |||||||
chr1:201984847 | T | G | 9 | a0001c0005t0001g0007 a0001c0005t0001g0055 a0001c0005t0001g0056 others(6): Show |
12 | HG02559.hp1 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.447+1734T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984847 | |||||||
chr1:201984866 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1753A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984866 | |||||||
chr1:201984883 | A | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1770A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984883 | |||||||
chr1:201984928 | C | T | 9 | a0001c0005t0001g0007 a0001c0005t0001g0055 a0001c0005t0001g0056 others(6): Show |
12 | HG02559.hp1 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.447+1815C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201984928 | |||||||
chr1:201985084 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+1971C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985084 | |||||||
chr1:201985191 | T | TA | 15 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0003t0001g0071 others(12): Show |
18 | HG01123.hp2 HG02559.hp1 HG02809.hp2 others(15): Show |
intron_variant | MODIFIER | c.447+2096dupA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201985191 | ||||||
chr1:201985191 | TA | T | 30 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0303 others(27): Show |
35 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.447+2096delA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201985191 | ||||||
chr1:201985191 | TAA | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.447+2095_447+2096d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201985191 | ||||||
chr1:201985211 | A | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(190): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.447+2098A>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985211 | |||||||
chr1:201985301 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+2188G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985301 | |||||||
chr1:201985307 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(93): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.447+2194T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985307 | |||||||
chr1:201985390 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+2277A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985390 | |||||||
chr1:201985394 | A | C | 1 | a0002c0002t0002g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.447+2281A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985394 | |||||||
chr1:201985412 | C | T | 1 | a0001c0001t0001g0358 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.447+2299C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985412 | |||||||
chr1:201985496 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(84): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.447+2383A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985496 | |||||||
chr1:201985504 | G | A | 59 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(56): Show |
67 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.447+2391G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985504 | |||||||
chr1:201985556 | T | G | 6 | a0001c0003t0001g0018 a0001c0003t0001g0042 a0001c0003t0001g0043 others(3): Show |
9 | HG00609.hp2 HG02083.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.447+2443T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985556 | |||||||
chr1:201985559 | A | C | 16 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(13): Show |
19 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+2446A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985559 | |||||||
chr1:201985569 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+2456C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985569 | |||||||
chr1:201985602 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+2489C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985602 | |||||||
chr1:201985603 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.447+2490T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985603 | |||||||
chr1:201985640 | T | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(78): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.447+2527T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985640 | |||||||
chr1:201985640 | T | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(93): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.447+2527T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985640 | |||||||
chr1:201985673 | A | G | 29 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(26): Show |
34 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.447+2560A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985673 | |||||||
chr1:201985679 | A | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(233): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.447+2566A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985679 | |||||||
chr1:201985696 | T | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(78): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.447+2583T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985696 | |||||||
chr1:201985859 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(78): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.447+2746C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985859 | |||||||
chr1:201985898 | C | G | 2 | a0001c0004t0001g0291 a0002c0002t0002g0290 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.447+2785C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985898 | |||||||
chr1:201985912 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(30): Show |
40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.447+2799G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985912 | |||||||
chr1:201985971 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.447+2858C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201985971 | |||||||
chr1:201986027 | A | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(56): Show |
67 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.448-2877A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986027 | |||||||
chr1:201986246 | GTTTTTTA others(1): Show |
G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.448-2645_448-2638d others(10): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201986246 | ||||||
chr1:201986433 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.448-2471G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986433 | |||||||
chr1:201986486 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.448-2418G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986486 | |||||||
chr1:201986528 | T | TTTTC | 20 | a0001c0001t0001g0155 a0001c0001t0001g0185 a0001c0003t0001g0176 others(17): Show |
20 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.448-2368_448-2365d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201986528 | ||||||
chr1:201986536 | C | CTTTCT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(106): Show |
128 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.448-2365_448-2364i others(7): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201986536 | ||||||
chr1:201986536 | C | CTTTCTT | 42 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(39): Show |
47 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.448-2365_448-2364i others(8): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201986536 | ||||||
chr1:201986538 | T | TTC | 14 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0051 others(11): Show |
17 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.448-2365_448-2364i others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201986538 | ||||||
chr1:201986539 | T | TC | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.448-2365_448-2364i others(3): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986539 | |||||||
chr1:201986540 | T | C | 6 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0003t0001g0231 others(3): Show |
7 | HG02258.hp1 HG02897.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.448-2364T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986540 | |||||||
chr1:201986661 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.448-2243C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986661 | |||||||
chr1:201986714 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.448-2190A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986714 | |||||||
chr1:201986715 | T | G | 1 | a0007c0016t0002g0233 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.448-2189T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986715 | |||||||
chr1:201986768 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.448-2136G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986768 | |||||||
chr1:201986901 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(68): Show |
82 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.448-2003C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201986901 | |||||||
chr1:201987089 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(240): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.448-1815T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987089 | |||||||
chr1:201987177 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.448-1727A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987177 | |||||||
chr1:201987189 | G | A | 15 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(12): Show |
18 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.448-1715G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987189 | |||||||
chr1:201987299 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.448-1605G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987299 | |||||||
chr1:201987428 | C | CT | 17 | a0001c0001t0001g0134 a0001c0003t0001g0010 a0001c0003t0001g0126 others(14): Show |
20 | HG01081.hp1 HG01243.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.448-1449dupT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | C | CTT | 10 | a0001c0001t0001g0140 a0001c0003t0001g0024 a0001c0003t0001g0025 others(7): Show |
12 | HG01106.hp1 HG01361.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.448-1450_448-1449d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | CT | C | 22 | a0001c0003t0001g0105 a0001c0003t0001g0106 a0001c0003t0001g0109 others(19): Show |
22 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.448-1449delT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | CTT | C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(37): Show |
48 | HG00609.hp1 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.448-1450_448-1449d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | CTTTTTTT others(2): Show |
C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(65): Show |
79 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.448-1457_448-1449d others(11): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | CTTTTTTT others(3): Show |
C | 28 | a0001c0001t0001g0308 a0001c0001t0001g0351 a0001c0001t0001g0352 others(25): Show |
32 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.448-1458_448-1449d others(12): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | CTTTTTTT others(4): Show |
C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.448-1459_448-1449d others(13): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987428 | CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0309 others(2): Show |
5 | HG01517.hp1 HG02818.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-1460_448-1449d others(14): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201987428 | ||||||
chr1:201987479 | C | A | 1 | a0001c0006t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.448-1425C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987479 | |||||||
chr1:201987554 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(30): Show |
40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.448-1350C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987554 | |||||||
chr1:201987625 | A | G | 1 | a0001c0003t0001g0074 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.448-1279A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987625 | |||||||
chr1:201987627 | A | G | 348 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(345): Show |
436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
intron_variant | MODIFIER | c.448-1277A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987627 | |||||||
chr1:201987690 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.448-1214G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987690 | |||||||
chr1:201987748 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.448-1156C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987748 | |||||||
chr1:201987802 | T | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(345): Show |
436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
intron_variant | MODIFIER | c.448-1102T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987802 | |||||||
chr1:201987903 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.448-1001A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987903 | |||||||
chr1:201987944 | C | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0044 others(14): Show |
26 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.448-960C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987944 | |||||||
chr1:201987954 | A | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(56): Show |
67 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.448-950A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987954 | |||||||
chr1:201987969 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0280 |
5 | NA18950.hp2 NA18987.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-935C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201987969 | |||||||
chr1:201988098 | C | A | 15 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(12): Show |
18 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.448-806C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988098 | |||||||
chr1:201988149 | A | AAAAAG | 29 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(26): Show |
34 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.448-743_448-739dup others(5): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201988149 | ||||||
chr1:201988232 | G | A | 1 | a0001c0003t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.448-672G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988232 | |||||||
chr1:201988353 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(75): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.448-551G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988353 | |||||||
chr1:201988373 | G | A | 1 | a0005c0011t0001g0033 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.448-531G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988373 | |||||||
chr1:201988437 | G | A | 29 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(26): Show |
34 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.448-467G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988437 | |||||||
chr1:201988457 | C | CA | 24 | a0001c0001t0001g0023 a0001c0001t0001g0078 a0001c0001t0001g0079 others(21): Show |
26 | HG00544.hp2 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.448-421dupA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201988457 | ||||||
chr1:201988457 | C | CAA | 20 | a0001c0001t0001g0134 a0001c0003t0001g0010 a0001c0003t0001g0025 others(17): Show |
24 | HG01081.hp1 HG01243.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.448-422_448-421dup others(2): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201988457 | ||||||
chr1:201988457 | C | CAAA | 11 | a0001c0001t0001g0140 a0001c0003t0001g0024 a0001c0003t0001g0054 others(8): Show |
12 | HG00735.hp1 HG01106.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.448-423_448-421dup others(3): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201988457 | ||||||
chr1:201988457 | CA | C | 54 | a0001c0001t0001g0017 a0001c0001t0001g0234 a0001c0001t0001g0237 others(51): Show |
65 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.448-421delA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201988457 | ||||||
chr1:201988457 | CAA | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.448-422_448-421del others(2): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 201988457 | ||||||
chr1:201988469 | A | C | 15 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(12): Show |
18 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.448-435A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988469 | |||||||
chr1:201988470 | A | C | 1 | a0001c0004t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.448-434A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988470 | |||||||
chr1:201988472 | A | C | 1 | a0001c0001t0001g0327 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.448-432A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988472 | |||||||
chr1:201988473 | A | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.448-431A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988473 | |||||||
chr1:201988477 | A | AC | 4 | a0001c0001t0001g0151 a0002c0002t0002g0186 a0002c0002t0002g0187 others(1): Show |
4 | HG00597.hp2 HG03927.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-427_448-426ins others(1): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988477 | |||||||
chr1:201988477 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(60): Show |
74 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.448-427A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988477 | |||||||
chr1:201988556 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.448-348A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988556 | |||||||
chr1:201988602 | G | A | 29 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(26): Show |
34 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.448-302G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988602 | |||||||
chr1:201988632 | C | A | 277 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.448-272C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 1/10 | chr1 | 201988632 | |||||||
chr1:201989066 | G | T | 1 | a0004c0008t0002g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.588+22G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/10 | chr1 | 201989066 | |||||||
chr1:201989140 | C | T | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0229 others(4): Show |
7 | HG00140.hp1 HG01069.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+96C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/10 | chr1 | 201989140 | |||||||
chr1:201989181 | C | A | 15 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(12): Show |
18 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.588+137C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/10 | chr1 | 201989181 | |||||||
chr1:201989184 | C | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0116 a0001c0003t0001g0083 others(5): Show |
8 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+140C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/10 | chr1 | 201989184 | |||||||
chr1:201989375 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02074.hp2 | splice_region_variant&intron_variant | LOW | c.589-8G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 2/10 | chr1 | 201989375 | |||||||
chr1:201989842 | AT | A | 15 | a0001c0001t0001g0084 a0001c0003t0001g0048 a0001c0003t0001g0049 others(12): Show |
18 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(15): Show |
intron_variant | MODIFIER | c.737+326delT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201989842 | ||||||
chr1:201989858 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.737+327G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201989858 | |||||||
chr1:201989994 | C | T | 1 | a0002c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.737+463C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201989994 | |||||||
chr1:201990005 | C | T | 3 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0002c0002t0002g0053 |
3 | HG02055.hp2 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.737+474C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990005 | |||||||
chr1:201990057 | C | A | 4 | a0002c0002t0002g0035 a0002c0002t0002g0244 a0002c0002t0002g0245 others(1): Show |
5 | HG00099.hp2 HG00323.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+526C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990057 | |||||||
chr1:201990060 | C | G | 4 | a0002c0002t0002g0035 a0002c0002t0002g0244 a0002c0002t0002g0245 others(1): Show |
5 | HG00099.hp2 HG00323.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+529C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990060 | |||||||
chr1:201990248 | C | T | 7 | a0001c0003t0001g0041 a0001c0003t0001g0231 a0001c0003t0001g0277 others(4): Show |
8 | HG01884.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.737+717C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990248 | |||||||
chr1:201990327 | G | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(93): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.737+796G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990327 | |||||||
chr1:201990345 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(38): Show |
49 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.737+814G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990345 | |||||||
chr1:201990362 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(54): Show |
65 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.737+831C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990362 | |||||||
chr1:201990416 | A | ACTTT | 5 | a0001c0001t0001g0308 a0001c0001t0001g0351 a0001c0001t0001g0352 others(2): Show |
5 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+885_737+886ins others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990416 | |||||||
chr1:201990419 | A | T | 5 | a0001c0001t0001g0308 a0001c0001t0001g0351 a0001c0001t0001g0352 others(2): Show |
5 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+888A>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990419 | |||||||
chr1:201990420 | A | C | 5 | a0001c0001t0001g0308 a0001c0001t0001g0351 a0001c0001t0001g0352 others(2): Show |
5 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+889A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990420 | |||||||
chr1:201990422 | G | GGAAACCT others(9): Show |
5 | a0001c0001t0001g0308 a0001c0001t0001g0351 a0001c0001t0001g0352 others(2): Show |
5 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+891_737+892ins others(16): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990422 | |||||||
chr1:201990610 | G | A | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(185): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.737+1079G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990610 | |||||||
chr1:201990650 | TA | T | 59 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(56): Show |
67 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.737+1120delA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990650 | |||||||
chr1:201990753 | C | T | 29 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0003t0001g0010 others(26): Show |
34 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.737+1222C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990753 | |||||||
chr1:201990864 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.737+1333G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990864 | |||||||
chr1:201990932 | C | G | 1 | a0001c0001t0003g0226 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.737+1401C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990932 | |||||||
chr1:201990951 | T | C | 4 | a0001c0003t0001g0249 a0002c0002t0002g0248 a0002c0002t0002g0250 others(1): Show |
4 | HG01433.hp1 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+1420T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990951 | |||||||
chr1:201990963 | A | T | 59 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(56): Show |
67 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.737+1432A>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990963 | |||||||
chr1:201990997 | C | A | 59 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(56): Show |
67 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.737+1466C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201990997 | |||||||
chr1:201991029 | T | G | 6 | a0001c0003t0001g0179 a0001c0003t0001g0217 a0001c0003t0001g0218 others(3): Show |
6 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+1498T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991029 | |||||||
chr1:201991058 | G | A | 2 | a0002c0002t0002g0196 a0002c0002t0002g0202 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.737+1527G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991058 | |||||||
chr1:201991141 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(84): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.737+1610G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991141 | |||||||
chr1:201991192 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(75): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.737+1661A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991192 | |||||||
chr1:201991200 | C | T | 1 | a0001c0003t0001g0318 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.737+1669C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991200 | |||||||
chr1:201991325 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0039 others(77): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.737+1794G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991325 | |||||||
chr1:201991365 | G | A | 1 | a0001c0003t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.737+1834G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991365 | |||||||
chr1:201991407 | G | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.737+1876G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991407 | |||||||
chr1:201991536 | G | T | 3 | a0001c0003t0001g0355 a0001c0003t0001g0356 a0001c0003t0001g0357 |
3 | HG01993.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.737+2005G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991536 | |||||||
chr1:201991562 | G | A | 2 | a0001c0003t0001g0176 a0001c0004t0001g0175 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.737+2031G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991562 | |||||||
chr1:201991619 | G | C | 8 | a0001c0005t0001g0007 a0001c0005t0001g0055 a0001c0005t0001g0056 others(5): Show |
11 | HG02559.hp1 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.737+2088G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991619 | |||||||
chr1:201991623 | G | T | 4 | a0002c0002t0002g0027 a0002c0002t0002g0153 a0002c0002t0002g0154 others(1): Show |
5 | NA18948.hp2 NA18963.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+2092G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991623 | |||||||
chr1:201991689 | G | T | 33 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0089 others(30): Show |
39 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.737+2158G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201991689 | |||||||
chr1:201992019 | T | TCTCC | 6 | a0001c0003t0001g0041 a0001c0003t0001g0277 a0001c0003t0001g0278 others(3): Show |
7 | HG01884.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.737+2508_737+2511d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201992019 | ||||||
chr1:201992284 | C | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0078 others(67): Show |
78 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.737+2753C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992284 | |||||||
chr1:201992558 | T | C | 1 | a0001c0003t0001g0297 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737+3027T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992558 | |||||||
chr1:201992583 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(73): Show |
101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.737+3052G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992583 | |||||||
chr1:201992614 | G | T | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.737+3083G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992614 | |||||||
chr1:201992618 | C | T | 1 | a0001c0003t0001g0179 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.737+3087C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992618 | |||||||
chr1:201992638 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.737+3107C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992638 | |||||||
chr1:201992645 | C | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(31): Show |
41 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.737+3114C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992645 | |||||||
chr1:201992701 | G | A | 1 | a0001c0003t0001g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.737+3170G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992701 | |||||||
chr1:201992751 | T | C | 21 | a0001c0003t0001g0041 a0001c0003t0001g0048 a0001c0003t0001g0049 others(18): Show |
25 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.737+3220T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201992751 | |||||||
chr1:201993146 | C | T | 2 | a0002c0002t0002g0016 a0002c0002t0002g0243 |
4 | NA18960.hp1 NA18975.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-3001C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993146 | |||||||
chr1:201993196 | T | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.738-2951T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993196 | |||||||
chr1:201993426 | A | G | 2 | a0002c0002t0002g0274 a0002c0002t0002g0275 |
2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.738-2721A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993426 | |||||||
chr1:201993451 | G | A | 1 | a0001c0003t0001g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.738-2696G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993451 | |||||||
chr1:201993453 | C | T | 1 | a0001c0003t0001g0349 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738-2694C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993453 | |||||||
chr1:201993463 | G | A | 1 | a0001c0003t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.738-2684G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993463 | |||||||
chr1:201993573 | G | A | 1 | a0001c0004t0001g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.738-2574G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993573 | |||||||
chr1:201993612 | C | CA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0147 others(67): Show |
77 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.738-2523dupA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201993612 | ||||||
chr1:201993612 | CA | C | 22 | a0001c0001t0001g0185 a0001c0001t0001g0192 a0001c0001t0001g0193 others(19): Show |
25 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.738-2523delA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201993612 | ||||||
chr1:201993652 | G | A | 1 | a0002c0002t0002g0331 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.738-2495G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993652 | |||||||
chr1:201993727 | C | T | 4 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0067 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-2420C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993727 | |||||||
chr1:201993758 | A | G | 12 | a0001c0001t0001g0308 a0001c0001t0001g0351 a0001c0001t0001g0352 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.738-2389A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993758 | |||||||
chr1:201993779 | A | G | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-2368A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993779 | |||||||
chr1:201993883 | G | T | 351 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(348): Show |
439 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(436): Show |
intron_variant | MODIFIER | c.738-2264G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993883 | |||||||
chr1:201993904 | A | AC | 9 | a0001c0001t0001g0023 a0001c0001t0001g0078 a0001c0001t0003g0273 others(6): Show |
11 | HG02080.hp1 HG02293.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.738-2236dupC | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201993904 | ||||||
chr1:201993931 | C | T | 1 | a0001c0003t0001g0050 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.738-2216C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993931 | |||||||
chr1:201993987 | A | G | 2 | a0001c0005t0001g0059 a0001c0005t0001g0060 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.738-2160A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201993987 | |||||||
chr1:201994032 | G | A | 3 | a0001c0001t0001g0252 a0002c0002t0002g0236 a0002c0002t0002g0253 |
3 | HG03688.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.738-2115G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994032 | |||||||
chr1:201994096 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.738-2051C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994096 | |||||||
chr1:201994172 | T | G | 1 | a0001c0003t0001g0050 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.738-1975T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994172 | |||||||
chr1:201994355 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.738-1792G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994355 | |||||||
chr1:201994442 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(341): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.738-1705T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994442 | |||||||
chr1:201994535 | G | C | 1 | a0001c0006t0001g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.738-1612G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994535 | |||||||
chr1:201994668 | C | CT | 9 | a0001c0003t0001g0049 a0001c0003t0001g0283 a0001c0003t0001g0285 others(6): Show |
12 | HG02559.hp1 HG02572.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.738-1463dupT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994668 | ||||||
chr1:201994668 | C | CTT | 13 | a0001c0003t0001g0048 a0001c0004t0001g0124 a0001c0004t0001g0130 others(10): Show |
13 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.738-1464_738-1463d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994668 | ||||||
chr1:201994668 | CT | C | 12 | a0001c0001t0001g0085 a0001c0001t0001g0280 a0001c0001t0001g0311 others(9): Show |
16 | HG00323.hp1 NA18522.hp1 NA18747.hp2 others(13): Show |
intron_variant | MODIFIER | c.738-1463delT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994668 | ||||||
chr1:201994670 | T | C | 11 | a0001c0003t0001g0216 a0002c0002t0002g0016 a0002c0002t0002g0177 others(8): Show |
13 | HG00597.hp2 HG00673.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.738-1477T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994670 | |||||||
chr1:201994787 | C | G | 13 | a0001c0004t0001g0124 a0001c0004t0001g0130 a0001c0004t0001g0135 others(10): Show |
13 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.738-1360C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994787 | |||||||
chr1:201994802 | G | C | 1 | a0001c0004t0001g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.738-1345G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994802 | |||||||
chr1:201994810 | G | A | 1 | a0001c0003t0001g0355 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.738-1337G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994810 | |||||||
chr1:201994833 | A | AT | 99 | a0001c0003t0001g0050 a0001c0003t0001g0067 a0001c0003t0001g0208 others(96): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.738-1288dupT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994833 | ||||||
chr1:201994833 | A | ATT | 19 | a0001c0004t0001g0175 a0001c0014t0001g0058 a0002c0002t0002g0011 others(16): Show |
22 | HG01109.hp2 HG01123.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.738-1289_738-1288d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994833 | ||||||
chr1:201994833 | A | ATTT | 7 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.738-1290_738-1288d others(5): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994833 | ||||||
chr1:201994833 | A | ATTTTT | 8 | a0001c0004t0001g0124 a0001c0004t0001g0130 a0001c0004t0001g0137 others(5): Show |
8 | HG00735.hp1 HG01361.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.738-1292_738-1288d others(7): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994833 | ||||||
chr1:201994833 | AT | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
206 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.738-1288delT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994833 | ||||||
chr1:201994833 | ATT | A | 11 | a0001c0001t0001g0234 a0001c0001t0001g0320 a0001c0001t0001g0322 others(8): Show |
12 | HG00609.hp2 HG02080.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.738-1289_738-1288d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201994833 | ||||||
chr1:201994856 | T | C | 4 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0001g0206 others(1): Show |
4 | HG01361.hp2 HG02735.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1291T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994856 | |||||||
chr1:201994931 | C | T | 1 | a0001c0014t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.738-1216C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994931 | |||||||
chr1:201994937 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0134 a0001c0001t0001g0140 others(6): Show |
11 | HG00544.hp1 NA18939.hp1 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.738-1210A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994937 | |||||||
chr1:201994960 | A | G | 357 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.738-1187A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994960 | |||||||
chr1:201994987 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.738-1160T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201994987 | |||||||
chr1:201995019 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
145 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.738-1128C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995019 | |||||||
chr1:201995054 | G | A | 41 | a0001c0003t0001g0041 a0001c0003t0001g0048 a0001c0003t0001g0049 others(38): Show |
46 | HG00140.hp1 HG01069.hp1 HG01361.hp2 others(43): Show |
intron_variant | MODIFIER | c.738-1093G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995054 | |||||||
chr1:201995105 | GTTTTGT | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(310): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(393): Show |
intron_variant | MODIFIER | c.738-1021_738-1016d others(8): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201995105 | ||||||
chr1:201995261 | G | A | 23 | a0002c0002t0001g0260 a0002c0002t0002g0002 a0002c0002t0002g0005 others(20): Show |
37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.738-886G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995261 | |||||||
chr1:201995425 | A | G | 357 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.738-722A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995425 | |||||||
chr1:201995484 | A | ACCAG | 9 | a0002c0002t0002g0011 a0002c0002t0002g0053 a0002c0002t0002g0286 others(6): Show |
12 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.738-658_738-655dup others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201995484 | ||||||
chr1:201995503 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
147 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.738-644C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995503 | |||||||
chr1:201995507 | AC | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
160 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.738-637delC | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 201995507 | ||||||
chr1:201995590 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG00558.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.738-557G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995590 | |||||||
chr1:201995598 | G | T | 13 | a0001c0004t0001g0124 a0001c0004t0001g0130 a0001c0004t0001g0135 others(10): Show |
13 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.738-549G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995598 | |||||||
chr1:201995684 | A | T | 4 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0219 others(1): Show |
4 | HG01891.hp1 HG01993.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-463A>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995684 | |||||||
chr1:201995741 | C | T | 1 | a0002c0002t0002g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.738-406C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995741 | |||||||
chr1:201995779 | T | A | 1 | a0002c0002t0001g0203 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.738-368T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995779 | |||||||
chr1:201995888 | C | A | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-259C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201995888 | |||||||
chr1:201996006 | C | T | 3 | a0002c0002t0001g0068 a0002c0002t0001g0070 a0002c0002t0001g0203 |
3 | HG02109.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.738-141C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201996006 | |||||||
chr1:201996020 | G | C | 1 | a0002c0013t0001g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.738-127G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201996020 | |||||||
chr1:201996097 | T | C | 2 | a0001c0003t0001g0178 a0001c0003t0001g0355 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.738-50T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 3/10 | chr1 | 201996097 | |||||||
chr1:201996465 | T | TGTGTGTG others(4): Show |
1 | a0002c0002t0002g0326 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.854+202_854+203ins others(11): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996465 | |||||||
chr1:201996465 | T | TGTGTGTG others(6): Show |
1 | a0002c0002t0002g0262 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.854+202_854+203ins others(13): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996465 | |||||||
chr1:201996465 | T | TTG | 12 | a0001c0001t0001g0064 a0001c0003t0001g0022 a0001c0003t0001g0067 others(9): Show |
13 | HG01167.hp2 HG02004.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.854+244_854+245dup others(2): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTG | 26 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0065 others(23): Show |
34 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.854+242_854+245dup others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTG | 26 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0085 others(23): Show |
28 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.854+240_854+245dup others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(1): Show |
45 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0063 others(42): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.854+238_854+245dup others(8): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(3): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(43): Show |
68 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.854+236_854+245dup others(10): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(5): Show |
25 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0158 others(22): Show |
29 | HG00558.hp2 HG00597.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.854+234_854+245dup others(12): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(7): Show |
32 | a0001c0001t0001g0026 a0001c0001t0001g0159 a0001c0001t0001g0229 others(29): Show |
36 | HG00099.hp1 HG00408.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.854+232_854+245dup others(14): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(9): Show |
12 | a0001c0001t0001g0157 a0001c0001t0001g0313 a0001c0003t0001g0357 others(9): Show |
15 | HG01070.hp2 HG01071.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.854+230_854+245dup others(16): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(11): Show |
5 | a0001c0001t0001g0312 a0001c0003t0001g0051 a0002c0002t0001g0070 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.854+228_854+245dup others(18): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | T | TTGTGTGT others(13): Show |
1 | a0002c0002t0001g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.854+226_854+245dup others(20): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTG | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0094 others(40): Show |
54 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.854+244_854+245del others(2): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTGTG | T | 3 | a0001c0003t0001g0109 a0001c0004t0001g0175 a0002c0002t0002g0242 |
3 | HG01109.hp2 NA18952.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.854+242_854+245del others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTGTGTG | T | 4 | a0001c0003t0001g0080 a0001c0003t0001g0133 a0002c0002t0002g0034 others(1): Show |
5 | HG00408.hp2 HG01243.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.854+240_854+245del others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0078 a0001c0001t0001g0358 others(2): Show |
6 | HG02559.hp2 HG03195.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.854+236_854+245del others(10): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTGTGTGT others(5): Show |
T | 10 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0066 others(7): Show |
13 | HG01891.hp2 HG02056.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.854+234_854+245del others(12): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTGTGTGT others(9): Show |
T | 2 | a0001c0003t0001g0207 a0001c0003t0001g0217 |
2 | HG03041.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.854+230_854+245del others(16): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996465 | TTGTGTGT others(11): Show |
T | 29 | a0001c0003t0001g0041 a0001c0003t0001g0050 a0001c0003t0001g0075 others(26): Show |
31 | HG00140.hp1 HG01069.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.854+228_854+245del others(18): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996465 | ||||||
chr1:201996504 | T | TGTGTGTG others(8): Show |
1 | a0002c0002t0002g0170 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.854+245_854+246ins others(15): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201996504 | ||||||
chr1:201996508 | T | TGTGTGTG others(4): Show |
3 | a0001c0001t0001g0116 a0001c0001t0001g0351 a0002c0002t0002g0270 |
3 | HG01109.hp1 HG02895.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.854+245_854+246ins others(11): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996508 | |||||||
chr1:201996508 | T | TGTGTGTG others(6): Show |
1 | a0002c0002t0002g0361 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.854+245_854+246ins others(13): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996508 | |||||||
chr1:201996508 | T | TGTGTGTG others(8): Show |
1 | a0002c0002t0002g0168 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.854+245_854+246ins others(15): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996508 | |||||||
chr1:201996508 | T | TGTGTGTG others(10): Show |
1 | a0002c0007t0002g0347 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.854+245_854+246ins others(17): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996508 | |||||||
chr1:201996533 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
229 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.854+270A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996533 | |||||||
chr1:201996554 | C | T | 1 | a0001c0003t0001g0235 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.854+291C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996554 | |||||||
chr1:201996582 | C | T | 31 | a0001c0003t0001g0041 a0001c0003t0001g0050 a0001c0003t0001g0075 others(28): Show |
33 | HG00140.hp1 HG01069.hp1 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.854+319C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996582 | |||||||
chr1:201996589 | G | A | 1 | a0002c0002t0002g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.854+326G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996589 | |||||||
chr1:201996596 | C | T | 1 | a0001c0003t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.854+333C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996596 | |||||||
chr1:201996628 | G | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0089 others(54): Show |
69 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.854+365G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996628 | |||||||
chr1:201996638 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0163 |
2 | NA18944.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.854+375C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996638 | |||||||
chr1:201996639 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0078 a0001c0001t0001g0358 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.854+376G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996639 | |||||||
chr1:201996708 | G | A | 2 | a0002c0002t0002g0214 a0002c0002t0002g0215 |
2 | NA18963.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.854+445G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996708 | |||||||
chr1:201996727 | C | T | 133 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(130): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.854+464C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996727 | |||||||
chr1:201996857 | C | T | 8 | a0001c0003t0001g0071 a0001c0003t0001g0083 a0001c0003t0001g0099 others(5): Show |
8 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.855-462C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201996857 | |||||||
chr1:201997110 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
147 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.855-209C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997110 | |||||||
chr1:201997111 | G | C | 1 | a0002c0002t0002g0027 | 2 | NA18948.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.855-208G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997111 | |||||||
chr1:201997145 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
147 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.855-174G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997145 | |||||||
chr1:201997167 | TG | T | 66 | a0002c0002t0001g0260 a0002c0002t0002g0002 a0002c0002t0002g0005 others(63): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.855-149delG | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 201997167 | ||||||
chr1:201997227 | G | A | 1 | a0001c0003t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.855-92G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997227 | |||||||
chr1:201997260 | G | A | 2 | a0001c0003t0001g0227 a0001c0003t0001g0296 |
2 | HG00140.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.855-59G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997260 | |||||||
chr1:201997289 | C | T | 1 | a0001c0004t0001g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.855-30C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997289 | |||||||
chr1:201997306 | C | T | 3 | a0001c0004t0001g0175 a0001c0004t0001g0288 a0001c0014t0001g0058 |
3 | HG01109.hp2 HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.855-13C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 4/10 | chr1 | 201997306 | |||||||
chr1:201997646 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0089 others(54): Show |
69 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1090+92T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997646 | |||||||
chr1:201997707 | A | C | 1 | a0002c0002t0002g0230 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1090+153A>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997707 | |||||||
chr1:201997740 | T | A | 1 | a0001c0004t0001g0139 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1090+186T>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997740 | |||||||
chr1:201997765 | A | AGTT | 3 | a0001c0003t0001g0022 a0001c0003t0001g0067 a0001c0003t0001g0077 |
4 | HG02818.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090+212_1090+214d others(5): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201997765 | ||||||
chr1:201997766 | G | GTT | 134 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(131): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1090+225_1090+226d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201997766 | ||||||
chr1:201997766 | G | GTTT | 67 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0089 others(64): Show |
78 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1090+224_1090+226d others(5): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201997766 | ||||||
chr1:201997766 | G | GTTTT | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
138 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1090+223_1090+226d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201997766 | ||||||
chr1:201997766 | G | GTTTTT | 7 | a0001c0001t0001g0078 a0001c0001t0001g0156 a0001c0001t0001g0314 others(4): Show |
7 | HG01175.hp1 HG01981.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+222_1090+226d others(7): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201997766 | ||||||
chr1:201997783 | G | C | 1 | a0002c0002t0002g0290 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1090+229G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997783 | |||||||
chr1:201997830 | C | T | 1 | a0001c0003t0001g0149 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1090+276C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997830 | |||||||
chr1:201997857 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
147 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1090+303G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997857 | |||||||
chr1:201997888 | C | T | 1 | a0002c0002t0002g0114 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1090+334C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201997888 | |||||||
chr1:201998054 | T | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(352): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.1090+500T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998054 | |||||||
chr1:201998087 | A | G | 1 | a0001c0001t0003g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1090+533A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998087 | |||||||
chr1:201998230 | C | CT | 156 | a0001c0003t0001g0041 a0001c0003t0001g0050 a0001c0003t0001g0051 others(153): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1090+697dupT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201998230 | ||||||
chr1:201998230 | C | CTT | 16 | a0001c0003t0001g0198 a0001c0004t0001g0124 a0001c0004t0001g0175 others(13): Show |
16 | HG00408.hp1 HG00735.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1090+696_1090+697d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201998230 | ||||||
chr1:201998230 | CT | C | 63 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0089 others(60): Show |
78 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1090+697delT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201998230 | ||||||
chr1:201998230 | CTTTT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
142 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1090+694_1090+697d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201998230 | ||||||
chr1:201998325 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
146 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1090+771G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998325 | |||||||
chr1:201998359 | A | T | 1 | a0001c0004t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1090+805A>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998359 | |||||||
chr1:201998415 | T | C | 3 | a0001c0003t0001g0041 a0001c0003t0001g0277 a0001c0005t0001g0055 |
4 | HG02717.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+861T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998415 | |||||||
chr1:201998541 | C | T | 126 | a0002c0002t0001g0068 a0002c0002t0001g0070 a0002c0002t0001g0203 others(123): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1090+987C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998541 | |||||||
chr1:201998542 | G | A | 57 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0089 others(54): Show |
69 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1090+988G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998542 | |||||||
chr1:201998748 | C | T | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-1154C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998748 | |||||||
chr1:201998794 | G | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
141 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1091-1108G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998794 | |||||||
chr1:201998860 | C | G | 2 | a0002c0002t0002g0165 a0002c0002t0002g0195 |
2 | HG01081.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1091-1042C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201998860 | |||||||
chr1:201999100 | C | T | 1 | a0002c0002t0002g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1091-802C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999100 | |||||||
chr1:201999110 | G | A | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-792G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999110 | |||||||
chr1:201999135 | T | C | 129 | a0001c0001t0001g0166 a0001c0003t0002g0092 a0002c0002t0001g0068 others(126): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1091-767T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999135 | |||||||
chr1:201999216 | C | CA | 34 | a0001c0001t0001g0192 a0001c0001t0001g0223 a0001c0001t0001g0315 others(31): Show |
41 | HG00597.hp2 HG00673.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1091-670dupA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 201999216 | ||||||
chr1:201999473 | C | A | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-429C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999473 | |||||||
chr1:201999499 | G | A | 52 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0022 others(49): Show |
61 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1091-403G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999499 | |||||||
chr1:201999556 | T | C | 49 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0024 others(46): Show |
57 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1091-346T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999556 | |||||||
chr1:201999722 | G | A | 1 | a0001c0003t0001g0357 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1091-180G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999722 | |||||||
chr1:201999837 | C | A | 1 | a0002c0002t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1091-65C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999837 | |||||||
chr1:201999868 | G | C | 1 | a0002c0002t0002g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1091-34G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999868 | |||||||
chr1:201999896 | C | G | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1091-6C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 5/10 | chr1 | 201999896 | |||||||
chr1:202000301 | A | G | 1 | a0002c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1204+286A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202000301 | |||||||
chr1:202000362 | G | A | 14 | a0001c0003t0001g0075 a0001c0003t0001g0076 a0001c0003t0001g0176 others(11): Show |
15 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1204+347G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202000362 | |||||||
chr1:202000582 | G | A | 2 | a0002c0002t0002g0153 a0002c0002t0002g0154 |
2 | NA18963.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1204+567G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202000582 | |||||||
chr1:202000785 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1205-591T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202000785 | |||||||
chr1:202000826 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1205-550A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202000826 | |||||||
chr1:202000893 | T | TA | 11 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0197 others(8): Show |
14 | HG01109.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1205-464dupA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 202000893 | ||||||
chr1:202000893 | T | TAAA | 40 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0024 others(37): Show |
48 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.1205-466_1205-464d others(5): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 202000893 | ||||||
chr1:202000893 | T | TAAAA | 10 | a0001c0003t0001g0022 a0001c0003t0001g0066 a0001c0003t0001g0071 others(7): Show |
11 | HG01123.hp2 HG01978.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1205-467_1205-464d others(6): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 202000893 | ||||||
chr1:202000893 | TA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
155 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1205-464delA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 202000893 | ||||||
chr1:202000893 | TAA | T | 121 | a0001c0001t0001g0040 a0001c0001t0001g0317 a0001c0001t0001g0343 others(118): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1205-465_1205-464d others(4): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 202000893 | ||||||
chr1:202000950 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
154 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1205-426G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202000950 | |||||||
chr1:202001288 | C | T | 1 | a0001c0003t0001g0022 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1205-88C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202001288 | |||||||
chr1:202001321 | G | A | 5 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0002c0002t0002g0213 others(2): Show |
7 | HG02040.hp2 HG02056.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205-55G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 6/10 | chr1 | 202001321 | |||||||
chr1:202001620 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
154 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1318-39G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 7/10 | chr1 | 202001620 | |||||||
chr1:202001829 | A | G | 1 | a0001c0014t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1426+62A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202001829 | |||||||
chr1:202001833 | G | A | 1 | a0002c0002t0002g0263 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1426+66G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202001833 | |||||||
chr1:202001858 | C | CA | 128 | a0001c0003t0002g0092 a0002c0002t0001g0068 a0002c0002t0001g0070 others(125): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1426+92dupA | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 202001858 | ||||||
chr1:202002165 | C | CT | 127 | a0001c0001t0001g0161 a0001c0003t0002g0092 a0002c0002t0001g0068 others(124): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1426+413dupT | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 202002165 | ||||||
chr1:202002220 | A | G | 124 | a0001c0003t0002g0092 a0002c0002t0001g0260 a0002c0002t0002g0002 others(121): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1426+453A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002220 | |||||||
chr1:202002352 | G | A | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1426+585G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002352 | |||||||
chr1:202002404 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
154 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1426+637C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002404 | |||||||
chr1:202002413 | C | T | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1426+646C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002413 | |||||||
chr1:202002586 | G | C | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427-651G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002586 | |||||||
chr1:202002592 | T | C | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427-645T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002592 | |||||||
chr1:202002656 | T | C | 2 | a0001c0003t0001g0178 a0001c0003t0001g0355 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1427-581T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002656 | |||||||
chr1:202002734 | C | T | 125 | a0001c0003t0002g0092 a0002c0002t0001g0260 a0002c0002t0002g0002 others(122): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1427-503C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002734 | |||||||
chr1:202002762 | G | C | 1 | a0001c0006t0001g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1427-475G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002762 | |||||||
chr1:202002856 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
149 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1427-381G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002856 | |||||||
chr1:202002953 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
154 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1427-284A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002953 | |||||||
chr1:202002963 | G | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0340 |
2 | HG00642.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1427-274G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002963 | |||||||
chr1:202002964 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0340 |
2 | HG00642.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1427-273C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202002964 | |||||||
chr1:202003039 | G | A | 42 | a0001c0003t0001g0041 a0001c0003t0001g0048 a0001c0003t0001g0049 others(39): Show |
47 | HG00140.hp1 HG01069.hp1 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.1427-198G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202003039 | |||||||
chr1:202003077 | C | T | 1 | a0001c0001t0001g0309 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1427-160C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 8/10 | chr1 | 202003077 | |||||||
chr1:202003613 | G | C | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651+152G>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202003613 | |||||||
chr1:202003726 | A | G | 1 | a0001c0004t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1651+265A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202003726 | |||||||
chr1:202003761 | C | T | 128 | a0001c0003t0002g0092 a0002c0002t0001g0068 a0002c0002t0001g0070 others(125): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1651+300C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202003761 | |||||||
chr1:202003827 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
154 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1651+366G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202003827 | |||||||
chr1:202003945 | T | C | 42 | a0001c0003t0001g0041 a0001c0003t0001g0048 a0001c0003t0001g0049 others(39): Show |
47 | HG00140.hp1 HG01069.hp1 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.1652-409T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202003945 | |||||||
chr1:202003993 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(310): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(393): Show |
intron_variant | MODIFIER | c.1652-361A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202003993 | |||||||
chr1:202004169 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0078 a0001c0001t0001g0358 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1652-185G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004169 | |||||||
chr1:202004214 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1652-140G>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004214 | |||||||
chr1:202004228 | A | G | 2 | a0001c0003t0001g0335 a0001c0003t0001g0342 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1652-126A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004228 | |||||||
chr1:202004241 | T | G | 2 | a0002c0002t0002g0095 a0002c0002t0002g0167 |
2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1652-113T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004241 | |||||||
chr1:202004270 | C | T | 4 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0219 others(1): Show |
4 | HG01891.hp1 HG01993.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1652-84C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004270 | |||||||
chr1:202004277 | C | T | 1 | a0001c0005t0001g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1652-77C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004277 | |||||||
chr1:202004317 | C | T | 1 | a0001c0012t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1652-37C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 9/10 | chr1 | 202004317 | |||||||
chr1:202004717 | A | G | 8 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0283 others(5): Show |
11 | HG02559.hp1 HG02572.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1794+221A>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202004717 | |||||||
chr1:202004833 | G | A | 65 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0022 others(62): Show |
74 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1794+337G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202004833 | |||||||
chr1:202004887 | C | T | 1 | a0001c0014t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1794+391C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202004887 | |||||||
chr1:202004936 | G | A | 5 | a0002c0002t0002g0011 a0002c0002t0002g0053 a0002c0002t0002g0286 others(2): Show |
8 | HG02055.hp2 HG02280.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1794+440G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202004936 | |||||||
chr1:202004946 | C | G | 1 | a0001c0003t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1794+450C>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202004946 | |||||||
chr1:202005002 | C | T | 6 | a0001c0003t0001g0150 a0001c0003t0001g0179 a0001c0003t0001g0217 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1794+506C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005002 | |||||||
chr1:202005011 | A | AGCATTGC others(3): Show |
1 | a0001c0001t0001g0328 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1794+520_1794+529d others(12): Show |
RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 202005011 | ||||||
chr1:202005050 | G | A | 5 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0279 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-508G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005050 | |||||||
chr1:202005164 | C | A | 13 | a0001c0004t0001g0124 a0001c0004t0001g0130 a0001c0004t0001g0135 others(10): Show |
13 | HG00735.hp1 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-394C>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005164 | |||||||
chr1:202005237 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0319 a0001c0001t0001g0325 others(4): Show |
9 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1795-321C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005237 | |||||||
chr1:202005238 | G | A | 15 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(12): Show |
18 | HG00609.hp1 HG00642.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1795-320G>A | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005238 | |||||||
chr1:202005314 | T | C | 65 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0022 others(62): Show |
74 | HG00544.hp2 HG00609.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1795-244T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005314 | |||||||
chr1:202005322 | T | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0280 |
5 | NA18950.hp2 NA18987.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-236T>G | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005322 | |||||||
chr1:202005375 | C | T | 355 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(352): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.1795-183C>T | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005375 | |||||||
chr1:202005538 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1795-20T>C | RNPEP | ENSG00000176393.11 | transcript | ENST00000295640.9 | protein_coding | 10/10 | chr1 | 202005538 |