Item | Value |
---|---|
geneid | 1380 |
ensemblid | ENSG00000117322.19 |
hgncid | 2336 |
symbol | CR2 |
name | complement C3d receptor 2 |
refseq_nuc | NM_001006658.3 |
refseq_prot | NP_001006659.1 |
ensembl_nuc | ENST00000367057.8 |
ensembl_prot | ENSP00000356024.3 |
mane_status | MANE Select |
chr | chr1 |
start | 207454328 |
end | 207489892 |
strand | + |
ver | v1.2 |
region | chr1:207454328-207489892 |
region5000 | chr1:207449328-207494892 |
regionname0 | CR2_chr1_207454328_207489892 |
regionname5000 | CR2_chr1_207449328_207494892 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1092 | 240 | 33 | 36 | 144 | 6 | 20 | 112 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0002 | 0/0 | 1092 | 86 | 36 | 14 | 28 | 2 | 6 | 22 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0003 | 0/0 | 1092 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0004 | 1/0 | 1092 | 6 | 0 | 3 | 0 | 1 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0005 | 0/0 | 1092 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0006 | 0/0 | 1092 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0007 | 0/0 | 1092 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0008 | 0/0 | 1092 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0009 | 0/0 | 1092 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0010 | 0/0 | 1092 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0011 | 0/0 | 1092 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0012 | 0/0 | 1092 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0013 | 0/0 | 1092 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0014 | 0/0 | 1092 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0015 | 0/0 | 1092 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0016 | 0/0 | 1092 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0017 | 0/0 | 1092 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0018 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0019 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0020 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0021 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0022 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0023 | 0/0 | 1092 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
a0024 | 0/0 | 1092 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | MGAAG others(1087): Show |
chr1 | 207449328 | 207494892 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3276 | 190 | 20 | 31 | 115 | 6 | 17 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0001c0003 | 0/0 | 3276 | 41 | 6 | 3 | 29 | 0 | 3 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0001c0007 | 0/0 | 3276 | 7 | 6 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0001c0016 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0001c0031 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0002c0002 | 0/0 | 3276 | 58 | 16 | 9 | 28 | 0 | 5 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0002c0004 | 0/0 | 3276 | 15 | 9 | 3 | 0 | 2 | 1 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0002c0005 | 0/0 | 3276 | 11 | 11 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0002c0013 | 0/0 | 3276 | 2 | 0 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0003c0006 | 0/0 | 3276 | 10 | 10 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0004c0008 | 1/0 | 3276 | 6 | 0 | 3 | 0 | 1 | 1 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0005c0010 | 0/0 | 3276 | 5 | 0 | 0 | 5 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0006c0009 | 0/0 | 3276 | 5 | 3 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0007c0012 | 0/0 | 3276 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0008c0011 | 0/0 | 3276 | 3 | 0 | 0 | 3 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0009c0023 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0009c0033 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0010c0015 | 0/0 | 3276 | 2 | 0 | 0 | 0 | 0 | 2 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0011c0025 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0011c0026 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0012c0014 | 0/0 | 3276 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0013c0022 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0014c0028 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0015c0017 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0016c0027 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0017c0024 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0018c0018 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0019c0021 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0020c0029 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0021c0030 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0022c0019 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0023c0020 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 | ||
a0024c0032 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | ATGGG others(3271): Show |
chr1 | 207449328 | 207494892 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4139 | 176 | 20 | 26 | 107 | 5 | 17 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0001t0003 | 0/0 | 4139 | 12 | 0 | 4 | 8 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0001t0006 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0001t0007 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0003t0001 | 0/0 | 4139 | 38 | 6 | 2 | 28 | 0 | 2 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0003t0003 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0003t0004 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0003t0005 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0007t0001 | 0/0 | 4139 | 4 | 3 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0007t0003 | 0/0 | 4139 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0016t0003 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0001c0031t0001 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0002c0002t0001 | 0/0 | 4139 | 10 | 10 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0002c0002t0002 | 0/0 | 4139 | 48 | 6 | 9 | 28 | 0 | 5 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0002c0004t0001 | 0/0 | 4139 | 15 | 9 | 3 | 0 | 2 | 1 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0002c0005t0001 | 0/0 | 4139 | 11 | 11 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0002c0013t0002 | 0/0 | 4139 | 2 | 0 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0003c0006t0001 | 0/0 | 4139 | 7 | 7 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0003c0006t0003 | 0/0 | 4139 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0004c0008t0003 | 1/0 | 4139 | 6 | 0 | 3 | 0 | 1 | 1 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0005c0010t0002 | 0/0 | 4139 | 5 | 0 | 0 | 5 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0006c0009t0001 | 0/0 | 4139 | 5 | 3 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0007c0012t0001 | 0/0 | 4139 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0007c0012t0003 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0008c0011t0003 | 0/0 | 4139 | 3 | 0 | 0 | 3 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0009c0023t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0009c0033t0003 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0010c0015t0002 | 0/0 | 4139 | 2 | 0 | 0 | 0 | 0 | 2 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0011c0025t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0011c0026t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0012c0014t0001 | 0/0 | 4139 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0013c0022t0002 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0014c0028t0001 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0015c0017t0001 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0016c0027t0001 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0017c0024t0001 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0018c0018t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0019c0021t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0020c0029t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0021c0030t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0022c0019t0001 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0023c0020t0001 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
a0024c0032t0001 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | AGCTG others(4134): Show |
chr1 | 207449328 | 207494892 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0003 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0011 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0017 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0003t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0007t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0016t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0001c0031t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0046 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0005t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0002c0013t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0003c0006t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0003c0006t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0003c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0003c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0003c0006t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0004c0008t0003g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0004c0008t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0004c0008t0003g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0005c0010t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0005c0010t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0005c0010t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0006c0009t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0006c0009t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0007c0012t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0007c0012t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0007c0012t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0008c0011t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0008c0011t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0009c0023t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0009c0033t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0010c0015t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0010c0015t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0011c0025t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0011c0026t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0012c0014t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0012c0014t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0013c0022t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0014c0028t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0015c0017t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0016c0027t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0017c0024t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0018c0018t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0019c0021t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0020c0029t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0021c0030t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0022c0019t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0023c0020t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
a0024c0032t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0022 | t0002 | g0005 | EUR | GBR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00140 | hp1 | a0002 | c0004 | t0001 | g0055 | EUR | GBR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0115 | EUR | FIN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00609 | hp1 | a0005 | c0010 | t0002 | g0001 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00639 | hp2 | a0004 | c0008 | t0003 | g0169 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0241 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00735 | hp2 | a0002 | c0004 | t0001 | g0059 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00741 | hp1 | a0014 | c0028 | t0001 | g0163 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01069 | hp2 | a0006 | c0009 | t0001 | g0038 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01070 | hp2 | a0004 | c0008 | t0003 | g0010 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01071 | hp1 | a0006 | c0009 | t0001 | g0038 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01081 | hp1 | a0015 | c0017 | t0001 | g0014 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01109 | hp1 | a0001 | c0003 | t0003 | g0211 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01168 | hp2 | a0002 | c0004 | t0001 | g0058 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01175 | hp2 | a0001 | c0031 | t0001 | g0269 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0233 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01257 | hp2 | a0001 | c0007 | t0001 | g0209 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01346 | hp2 | a0002 | c0013 | t0002 | g0005 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01358 | hp1 | a0002 | c0004 | t0001 | g0026 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01361 | hp1 | a0004 | c0008 | t0003 | g0010 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01361 | hp2 | a0002 | c0013 | t0002 | g0005 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0191 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01496 | hp1 | a0016 | c0027 | t0001 | g0003 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01891 | hp1 | a0001 | c0007 | t0003 | g0194 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0069 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02040 | hp2 | a0017 | c0024 | t0001 | g0053 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02055 | hp2 | a0001 | c0007 | t0003 | g0193 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02145 | hp1 | a0009 | c0023 | t0001 | g0263 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CDX | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02257 | hp2 | a0001 | c0007 | t0003 | g0187 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02258 | hp1 | a0006 | c0009 | t0001 | g0018 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02451 | hp1 | a0003 | c0006 | t0003 | g0020 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0265 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02572 | hp1 | a0007 | c0012 | t0001 | g0223 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02572 | hp2 | a0002 | c0004 | t0001 | g0024 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02602 | hp1 | a0010 | c0015 | t0002 | g0251 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02615 | hp2 | a0002 | c0005 | t0001 | g0258 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02622 | hp1 | a0002 | c0005 | t0001 | g0022 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02622 | hp2 | a0002 | c0004 | t0001 | g0056 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02630 | hp1 | a0018 | c0018 | t0001 | g0255 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02630 | hp2 | a0011 | c0026 | t0001 | g0213 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02717 | hp1 | a0002 | c0004 | t0001 | g0228 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0184 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02809 | hp1 | a0002 | c0004 | t0001 | g0024 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02809 | hp2 | a0003 | c0006 | t0001 | g0221 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02818 | hp1 | a0002 | c0004 | t0001 | g0224 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02818 | hp2 | a0002 | c0005 | t0001 | g0253 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02895 | hp1 | a0002 | c0005 | t0001 | g0049 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02896 | hp1 | a0002 | c0004 | t0001 | g0227 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02896 | hp2 | a0001 | c0016 | t0003 | g0186 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02897 | hp1 | a0002 | c0005 | t0001 | g0049 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02897 | hp2 | a0002 | c0004 | t0001 | g0226 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02922 | hp1 | a0003 | c0006 | t0001 | g0044 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02922 | hp2 | a0002 | c0005 | t0001 | g0254 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02970 | hp1 | a0001 | c0007 | t0001 | g0195 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03041 | hp2 | a0007 | c0012 | t0001 | g0222 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03139 | hp1 | a0001 | c0007 | t0001 | g0196 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03195 | hp1 | a0003 | c0006 | t0001 | g0021 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03209 | hp1 | a0019 | c0021 | t0001 | g0260 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03209 | hp2 | a0020 | c0029 | t0001 | g0259 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03225 | hp1 | a0007 | c0012 | t0003 | g0054 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03225 | hp2 | a0006 | c0009 | t0001 | g0018 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03239 | hp1 | a0002 | c0004 | t0001 | g0026 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0247 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03453 | hp2 | a0021 | c0030 | t0001 | g0062 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03486 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03491 | hp1 | a0004 | c0008 | t0003 | g0010 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0182 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0181 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0180 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03516 | hp2 | a0022 | c0019 | t0001 | g0025 | AFR | ESN | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03540 | hp1 | a0002 | c0005 | t0001 | g0257 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03579 | hp1 | a0002 | c0005 | t0001 | g0050 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03579 | hp2 | a0003 | c0006 | t0003 | g0020 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03710 | hp2 | a0001 | c0003 | t0005 | g0201 | SAS | PJL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03831 | hp2 | a0010 | c0015 | t0002 | g0005 | SAS | BEB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG04204 | hp1 | a0023 | c0020 | t0001 | g0057 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18522 | hp1 | a0001 | c0007 | t0001 | g0207 | AFR | YRI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | YRI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18906 | hp1 | a0009 | c0033 | t0003 | g0256 | AFR | YRI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18906 | hp2 | a0002 | c0004 | t0001 | g0025 | AFR | YRI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18940 | hp2 | a0008 | c0011 | t0003 | g0153 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18942 | hp1 | a0012 | c0014 | t0001 | g0003 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18943 | hp2 | a0008 | c0011 | t0003 | g0042 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18963 | hp2 | a0012 | c0014 | t0001 | g0083 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18970 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18977 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18979 | hp1 | a0001 | c0003 | t0004 | g0200 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18983 | hp2 | a0008 | c0011 | t0003 | g0042 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18987 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18988 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19006 | hp1 | a0005 | c0010 | t0002 | g0012 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19009 | hp1 | a0005 | c0010 | t0002 | g0249 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | LWK | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19030 | hp2 | a0003 | c0006 | t0001 | g0021 | AFR | LWK | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19043 | hp1 | a0002 | c0004 | t0001 | g0225 | AFR | LWK | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19043 | hp2 | a0003 | c0006 | t0001 | g0021 | AFR | LWK | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19055 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0189 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19063 | hp1 | a0024 | c0032 | t0001 | g0109 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19064 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19077 | hp1 | a0005 | c0010 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19084 | hp1 | a0005 | c0010 | t0002 | g0001 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA19240 | hp2 | a0003 | c0006 | t0003 | g0020 | AFR | YRI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20129 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | ASW | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20752 | hp1 | a0004 | c0008 | t0003 | g0010 | EUR | TSI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20752 | hp2 | a0002 | c0004 | t0001 | g0060 | EUR | TSI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02109 | hp1 | a0003 | c0006 | t0001 | g0052 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0236 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0252 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG02559 | hp2 | a0002 | c0005 | t0001 | g0050 | AFR | ACB | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0250 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA20300 | hp2 | a0003 | c0006 | t0001 | g0044 | AFR | USA | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA21309 | hp1 | a0011 | c0025 | t0001 | g0066 | AFR | LWK | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
NA21309 | hp2 | a0006 | c0009 | t0001 | g0018 | AFR | LWK | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0077 | REF | REF | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
homoSapiens | grch38p0 | a0004 | c0008 | t0003 | g0261 | REF | REF | CR2_chr1_207449328_207494892 | CR2 | chr1 | 207449328 | 207494892 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:207466667 | C | G | 1 | a0005 | 5 | HG00609.hp1 NA19006.hp1 NA19009.hp1 others(2): Show |
missense_variant | MODERATE | c.200C>G | p.Thr67Ser | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/20 | 291/4139 | 200/3279 | 67/1092 | chr1 | 207466667 | |||
chr1:207466843 | G | A | 1 | a0015 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.376G>A | p.Gly126Arg | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/20 | 467/4139 | 376/3279 | 126/1092 | chr1 | 207466843 | |||
chr1:207468605 | C | T | 1 | a0010 | 2 | HG02602.hp1 HG03831.hp2 |
missense_variant | MODERATE | c.524C>T | p.Pro175Leu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 3/20 | 615/4139 | 524/3279 | 175/1092 | chr1 | 207468605 | |||
chr1:207468680 | C | T | 1 | a0024 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.599C>T | p.Ser200Leu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 3/20 | 690/4139 | 599/3279 | 200/1092 | chr1 | 207468680 | |||
chr1:207468806 | G | A | 1 | a0008 | 3 | NA18940.hp2 NA18943.hp2 NA18983.hp2 |
missense_variant | MODERATE | c.641G>A | p.Arg214His | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 4/20 | 732/4139 | 641/3279 | 214/1092 | chr1 | 207468806 | |||
chr1:207469989 | A | G | 1 | a0021 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1112A>G | p.Tyr371Cys | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/20 | 1203/4139 | 1112/3279 | 371/1092 | chr1 | 207469989 | |||
chr1:207471069 | A | G | 1 | a0020 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1475A>G | p.Asn492Ser | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 8/20 | 1566/4139 | 1475/3279 | 492/1092 | chr1 | 207471069 | |||
chr1:207472823 | G | T | 1 | a0006 | 5 | HG01069.hp2 HG01071.hp1 HG02258.hp1 others(2): Show |
missense_variant | MODERATE | c.1622G>T | p.Ser541Ile | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/20 | 1713/4139 | 1622/3279 | 541/1092 | chr1 | 207472823 | |||
chr1:207473117 | G | A | 10 | a0002 a0005 a0009 others(7): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
missense_variant | MODERATE | c.1916G>A | p.Ser639Asn | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/20 | 2007/4139 | 1916/3279 | 639/1092 | chr1 | 207473117 | |||
chr1:207473553 | T | C | 13 | a0002 a0003 a0005 others(10): Show |
115 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(112): Show |
missense_variant | MODERATE | c.1987T>C | p.Ser663Pro | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 11/20 | 2078/4139 | 1987/3279 | 663/1092 | chr1 | 207473553 | |||
chr1:207473578 | G | A | 10 | a0002 a0005 a0009 others(7): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
missense_variant | MODERATE | c.2012G>A | p.Arg671His | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 11/20 | 2103/4139 | 2012/3279 | 671/1092 | chr1 | 207473578 | |||
chr1:207473863 | G | A | 1 | a0018 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2218G>A | p.Val740Ile | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 12/20 | 2309/4139 | 2218/3279 | 740/1092 | chr1 | 207473863 | |||
chr1:207475111 | G | T | 1 | a0023 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2611G>T | p.Val871Leu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/20 | 2702/4139 | 2611/3279 | 871/1092 | chr1 | 207475111 | |||
chr1:207475128 | T | G | 1 | a0016 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2628T>G | p.Asn876Lys | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/20 | 2719/4139 | 2628/3279 | 876/1092 | chr1 | 207475128 | |||
chr1:207475211 | A | G | 1 | a0022 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2711A>G | p.Lys904Arg | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/20 | 2802/4139 | 2711/3279 | 904/1092 | chr1 | 207475211 | |||
chr1:207476353 | G | A | 1 | a0019 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2836G>A | p.Val946Met | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/20 | 2927/4139 | 2836/3279 | 946/1092 | chr1 | 207476353 | |||
chr1:207478015 | G | C | 1 | a0017 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.3033G>C | p.Gln1011His | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/20 | 3124/4139 | 3033/3279 | 1011/1092 | chr1 | 207478015 | |||
chr1:207479987 | C | T | 1 | a0012 | 2 | NA18942.hp1 NA18963.hp2 |
missense_variant | MODERATE | c.3122C>T | p.Ala1041Val | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/20 | 3213/4139 | 3122/3279 | 1041/1092 | chr1 | 207479987 | |||
chr1:207480019 | A | G | 5 | a0007 a0009 a0011 others(2): Show |
9 | HG00741.hp1 HG02040.hp2 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.3154A>G | p.Ile1052Val | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/20 | 3245/4139 | 3154/3279 | 1052/1092 | chr1 | 207480019 | |||
chr1:207480050 | C | A | 22 | a0001 a0002 a0003 others(19): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
missense_variant | MODERATE | c.3185C>A | p.Ala1062Glu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/20 | 3276/4139 | 3185/3279 | 1062/1092 | chr1 | 207480050 | |||
chr1:207480052 | C | T | 1 | a0013 | 1 | HG00099.hp1 | missense_variant&splice_region_variant | MODERATE | c.3187C>T | p.Arg1063Cys | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/20 | 3278/4139 | 3187/3279 | 1063/1092 | chr1 | 207480052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:207466548 | G | A | 1 | a0001c0016 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.81G>A | p.Pro27Pro | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/20 | 172/4139 | 81/3279 | 27/1092 | chr1 | 207466548 | |||
chr1:207466656 | A | G | 1 | a0009c0033 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.189A>G | p.Leu63Leu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/20 | 280/4139 | 189/3279 | 63/1092 | chr1 | 207466656 | |||
chr1:207468705 | C | G | 1 | a0001c0031 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.624C>G | p.Pro208Pro | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 3/20 | 715/4139 | 624/3279 | 208/1092 | chr1 | 207468705 | |||
chr1:207472818 | C | T | 1 | a0001c0007 | 7 | HG01257.hp2 HG01891.hp1 HG02055.hp2 others(4): Show |
synonymous_variant | LOW | c.1617C>T | p.Thr539Thr | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/20 | 1708/4139 | 1617/3279 | 539/1092 | chr1 | 207472818 | |||
chr1:207472977 | G | A | 23 | a0001c0003 a0001c0007 a0001c0016 others(20): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(164): Show |
synonymous_variant | LOW | c.1776G>A | p.Leu592Leu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/20 | 1867/4139 | 1776/3279 | 592/1092 | chr1 | 207472977 | |||
chr1:207474828 | T | C | 3 | a0002c0004 a0022c0019 a0023c0020 |
17 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(14): Show |
synonymous_variant | LOW | c.2328T>C | p.Ile776Ile | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/20 | 2419/4139 | 2328/3279 | 776/1092 | chr1 | 207474828 | |||
chr1:207475149 | T | C | 3 | a0002c0005 a0009c0033 a0018c0018 |
13 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
synonymous_variant | LOW | c.2649T>C | p.Gly883Gly | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/20 | 2740/4139 | 2649/3279 | 883/1092 | chr1 | 207475149 | |||
chr1:207475194 | T | C | 1 | a0011c0025 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2694T>C | p.Gly898Gly | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/20 | 2785/4139 | 2694/3279 | 898/1092 | chr1 | 207475194 | |||
chr1:207476361 | G | A | 1 | a0002c0013 | 2 | HG01346.hp2 HG01361.hp2 |
synonymous_variant | LOW | c.2844G>A | p.Glu948Glu | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/20 | 2935/4139 | 2844/3279 | 948/1092 | chr1 | 207476361 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:207454348 | T | C | 5 | a0002c0002t0002 a0002c0013t0002 a0005c0010t0002 others(2): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/20 | chr1 | 207454348 | |||||||
chr1:207454353 | C | T | 1 | a0001c0001t0007 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/20 | 66 | chr1 | 207454353 | ||||||
chr1:207454365 | C | T | 1 | a0001c0001t0006 | 1 | HG01978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/20 | 54 | chr1 | 207454365 | ||||||
chr1:207489567 | T | C | 33 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(30): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*444T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 20/20 | 4013 | chr1 | 207489567 | ||||||
chr1:207489567 | T | G | 1 | a0001c0003t0005 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 20/20 | 4013 | chr1 | 207489567 | ||||||
chr1:207489684 | T | C | 1 | a0001c0003t0004 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 20/20 | 4130 | chr1 | 207489684 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:207454529 | T | C | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58+53T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207454529 | |||||||
chr1:207454573 | G | A | 10 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0026 others(7): Show |
12 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+97G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207454573 | |||||||
chr1:207454653 | C | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0031t0001g0269 |
3 | HG00741.hp2 HG01175.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.58+177C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207454653 | |||||||
chr1:207454731 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.58+255G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207454731 | |||||||
chr1:207454766 | G | A | 2 | a0001c0003t0001g0027 a0021c0030t0001g0062 |
3 | HG01243.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.58+290G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207454766 | |||||||
chr1:207454949 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.58+473A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207454949 | |||||||
chr1:207455307 | T | C | 1 | a0003c0006t0001g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58+831T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207455307 | |||||||
chr1:207455443 | A | T | 2 | a0001c0003t0001g0265 a0001c0003t0001g0266 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58+967A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207455443 | |||||||
chr1:207455524 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.58+1048A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207455524 | |||||||
chr1:207455548 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.58+1072A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207455548 | |||||||
chr1:207455549 | T | C | 1 | a0002c0004t0001g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.58+1073T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207455549 | |||||||
chr1:207456071 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.58+1595T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456071 | |||||||
chr1:207456169 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.58+1693G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456169 | |||||||
chr1:207456178 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.58+1702G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456178 | |||||||
chr1:207456214 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.58+1738T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456214 | |||||||
chr1:207456349 | T | C | 1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.58+1873T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456349 | |||||||
chr1:207456357 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.58+1881A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456357 | |||||||
chr1:207456518 | A | G | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58+2042A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456518 | |||||||
chr1:207456656 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.58+2180C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456656 | |||||||
chr1:207456687 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.58+2211G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456687 | |||||||
chr1:207456949 | A | G | 1 | a0002c0005t0001g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.58+2473A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207456949 | |||||||
chr1:207457099 | C | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.58+2623C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457099 | |||||||
chr1:207457150 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.58+2674C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457150 | |||||||
chr1:207457172 | G | T | 1 | a0001c0003t0001g0043 | 2 | NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.58+2696G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457172 | |||||||
chr1:207457491 | C | T | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58+3015C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457491 | |||||||
chr1:207457543 | C | A | 15 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0026 others(12): Show |
17 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.58+3067C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457543 | |||||||
chr1:207457570 | G | T | 1 | a0007c0012t0003g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58+3094G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457570 | |||||||
chr1:207457614 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.58+3138T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457614 | |||||||
chr1:207457703 | T | A | 7 | a0001c0003t0001g0027 a0003c0006t0001g0021 a0003c0006t0001g0044 others(4): Show |
13 | HG01243.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+3227T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457703 | |||||||
chr1:207457782 | C | CT | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3312dupT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207457782 | ||||||
chr1:207457813 | T | A | 37 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0008 others(34): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.58+3337T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457813 | |||||||
chr1:207457842 | T | C | 1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+3366T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457842 | |||||||
chr1:207457860 | A | G | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0008 others(43): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.58+3384A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457860 | |||||||
chr1:207457987 | A | T | 9 | a0002c0005t0001g0022 a0002c0005t0001g0049 a0002c0005t0001g0050 others(6): Show |
13 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+3511A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207457987 | |||||||
chr1:207458054 | G | A | 1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+3578G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458054 | |||||||
chr1:207458059 | A | AAC | 6 | a0002c0002t0002g0005 a0002c0002t0002g0252 a0002c0013t0002g0005 others(3): Show |
8 | HG00099.hp1 HG01346.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+3622_58+3623dup others(2): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACAC | 14 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(11): Show |
16 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.58+3620_58+3623dup others(4): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACAC | 16 | a0001c0001t0001g0037 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
28 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.58+3618_58+3623dup others(6): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(1): Show |
19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0065 others(16): Show |
23 | HG00408.hp2 HG00639.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.58+3616_58+3623dup others(8): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(3): Show |
56 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0017 others(53): Show |
83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.58+3614_58+3623dup others(10): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(5): Show |
59 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.58+3612_58+3623dup others(12): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(7): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0078 others(26): Show |
33 | HG00408.hp1 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+3610_58+3623dup others(14): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(9): Show |
6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG02818.hp2 HG04199.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3608_58+3623dup others(16): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(11): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | NA18949.hp2 NA18966.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.58+3606_58+3623dup others(18): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(13): Show |
2 | a0001c0001t0006g0069 a0002c0004t0001g0224 |
2 | HG01978.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.58+3604_58+3623dup others(20): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | AACACACA others(21): Show |
1 | a0001c0001t0001g0068 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+3596_58+3623dup others(28): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0214 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.58+3583_58+3584ins others(13): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458059 | |||||||
chr1:207458059 | AAC | A | 6 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(3): Show |
13 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+3622_58+3623del others(2): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458059 | AACACACA others(11): Show |
A | 1 | a0008c0011t0003g0042 | 2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.58+3606_58+3623del others(18): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458059 | ||||||
chr1:207458063 | C | CACACACA others(17): Show |
1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.58+3610_58+3611ins others(24): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458063 | ||||||
chr1:207458067 | C | CACACACA others(15): Show |
1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.58+3612_58+3613ins others(22): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458067 | ||||||
chr1:207458071 | C | CACACACA others(31): Show |
1 | a0001c0003t0001g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58+3612_58+3613ins others(38): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458071 | ||||||
chr1:207458071 | C | CACACACA others(9): Show |
1 | a0003c0006t0001g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58+3610_58+3611ins others(16): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458071 | ||||||
chr1:207458073 | C | CACACACA others(27): Show |
1 | a0001c0003t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58+3616_58+3617ins others(34): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458073 | ||||||
chr1:207458073 | C | CACACACA others(29): Show |
1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+3614_58+3615ins others(36): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458073 | ||||||
chr1:207458073 | C | CACACACA others(25): Show |
3 | a0001c0003t0001g0184 a0001c0003t0001g0185 a0001c0016t0003g0186 |
3 | HG02257.hp1 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.58+3614_58+3615ins others(32): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458073 | ||||||
chr1:207458073 | C | CACACACA others(31): Show |
1 | a0001c0003t0003g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.58+3612_58+3613ins others(38): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458073 | ||||||
chr1:207458073 | C | CACACACA others(29): Show |
1 | a0001c0003t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58+3612_58+3613ins others(36): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458073 | ||||||
chr1:207458073 | C | CACACACA others(25): Show |
1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.58+3606_58+3607ins others(32): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458073 | ||||||
chr1:207458075 | C | CACACACA others(23): Show |
1 | a0001c0007t0003g0187 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58+3614_58+3615ins others(30): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458075 | ||||||
chr1:207458077 | C | CACACACA others(22): Show |
1 | a0001c0003t0001g0067 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.58+3614_58+3615ins others(29): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACACA others(23): Show |
3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG03491.hp2 HG03492.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.58+3616_58+3617ins others(30): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACACA others(21): Show |
28 | a0001c0003t0001g0019 a0001c0003t0001g0039 a0001c0003t0001g0040 others(25): Show |
34 | HG00673.hp1 HG01257.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+3614_58+3615ins others(28): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACACA others(25): Show |
2 | a0003c0006t0001g0044 a0003c0006t0001g0221 |
3 | HG02809.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58+3610_58+3611ins others(32): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACACA others(17): Show |
1 | a0001c0003t0001g0212 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.58+3610_58+3611ins others(24): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACAT | 3 | a0001c0003t0001g0027 a0003c0006t0001g0021 a0021c0030t0001g0062 |
6 | HG01243.hp1 HG03195.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+3606_58+3607ins others(6): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACATA others(25): Show |
1 | a0003c0006t0003g0020 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.58+3606_58+3607ins others(32): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458077 | C | CACACATA others(21): Show |
1 | a0007c0012t0001g0222 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58+3606_58+3607ins others(28): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458077 | ||||||
chr1:207458099 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.58+3623_58+3624ins others(11): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458099 | |||||||
chr1:207458277 | A | AT | 6 | a0001c0003t0003g0211 a0002c0002t0002g0250 a0002c0004t0001g0025 others(3): Show |
6 | HG01109.hp1 HG02622.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3814dupT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458277 | ||||||
chr1:207458277 | AT | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.58+3814delT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207458277 | ||||||
chr1:207458317 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.58+3841A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458317 | |||||||
chr1:207458331 | C | T | 1 | a0002c0004t0001g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3855C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458331 | |||||||
chr1:207458332 | G | A | 1 | a0007c0012t0001g0222 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58+3856G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458332 | |||||||
chr1:207458408 | C | T | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58+3932C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458408 | |||||||
chr1:207458433 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.58+3957T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458433 | |||||||
chr1:207458606 | T | C | 5 | a0002c0004t0001g0224 a0002c0004t0001g0225 a0002c0004t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+4130T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458606 | |||||||
chr1:207458746 | C | T | 2 | a0001c0003t0001g0183 a0001c0003t0001g0210 |
2 | HG02027.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.58+4270C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458746 | |||||||
chr1:207458784 | G | C | 1 | a0002c0004t0001g0024 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.58+4308G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458784 | |||||||
chr1:207458885 | T | A | 1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.58+4409T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458885 | |||||||
chr1:207458952 | C | G | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.58+4476C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207458952 | |||||||
chr1:207459142 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.58+4666A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459142 | |||||||
chr1:207459181 | G | C | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58+4705G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459181 | |||||||
chr1:207459321 | G | GT | 27 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0131 others(24): Show |
45 | HG00558.hp2 HG00639.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.58+4856dupT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207459321 | ||||||
chr1:207459324 | T | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0162 a0001c0001t0001g0172 |
3 | HG02056.hp1 NA18944.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.58+4848T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459324 | |||||||
chr1:207459451 | A | G | 18 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0026 others(15): Show |
20 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+4975A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459451 | |||||||
chr1:207459460 | T | C | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58+4984T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459460 | |||||||
chr1:207459544 | T | C | 1 | a0003c0006t0003g0020 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.58+5068T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459544 | |||||||
chr1:207459566 | G | C | 1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+5090G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459566 | |||||||
chr1:207459599 | T | C | 1 | a0001c0003t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.58+5123T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459599 | |||||||
chr1:207459610 | C | T | 1 | a0001c0007t0001g0209 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.58+5134C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459610 | |||||||
chr1:207459788 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.58+5312A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459788 | |||||||
chr1:207459849 | T | C | 2 | a0001c0003t0001g0265 a0001c0003t0001g0266 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58+5373T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459849 | |||||||
chr1:207459939 | T | G | 2 | a0001c0003t0001g0181 a0001c0003t0001g0182 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.58+5463T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207459939 | |||||||
chr1:207460143 | T | G | 1 | a0001c0003t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58+5667T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207460143 | |||||||
chr1:207460176 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0099 others(1): Show |
4 | HG00558.hp1 HG02523.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5700G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207460176 | |||||||
chr1:207460502 | A | G | 1 | a0002c0005t0001g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.59-6024A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207460502 | |||||||
chr1:207460530 | A | G | 2 | a0003c0006t0001g0052 a0007c0012t0003g0054 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-5996A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207460530 | |||||||
chr1:207460929 | T | C | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-5597T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207460929 | |||||||
chr1:207460949 | A | G | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-5577A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207460949 | |||||||
chr1:207461100 | G | A | 1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59-5426G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461100 | |||||||
chr1:207461118 | GT | G | 5 | a0002c0004t0001g0224 a0002c0004t0001g0225 a0002c0004t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-5401delT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207461118 | ||||||
chr1:207461138 | G | T | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-5388G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461138 | |||||||
chr1:207461272 | A | G | 2 | a0001c0003t0001g0265 a0001c0003t0001g0266 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.59-5254A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461272 | |||||||
chr1:207461308 | A | T | 1 | a0002c0002t0002g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-5218A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461308 | |||||||
chr1:207461325 | T | C | 38 | a0001c0003t0001g0019 a0001c0003t0001g0039 a0001c0003t0001g0040 others(35): Show |
44 | HG00673.hp1 HG01257.hp2 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.59-5201T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461325 | |||||||
chr1:207461330 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59-5196G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461330 | |||||||
chr1:207461542 | G | A | 1 | a0002c0002t0002g0048 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.59-4984G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461542 | |||||||
chr1:207461742 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.59-4784G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461742 | |||||||
chr1:207461831 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-4695C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207461831 | |||||||
chr1:207462045 | G | A | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-4481G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462045 | |||||||
chr1:207462101 | T | C | 1 | a0010c0015t0002g0251 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.59-4425T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462101 | |||||||
chr1:207462228 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.59-4298A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462228 | |||||||
chr1:207462288 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
9 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-4238C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462288 | |||||||
chr1:207462339 | C | T | 1 | a0002c0004t0001g0024 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.59-4187C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462339 | |||||||
chr1:207462444 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.59-4082T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462444 | |||||||
chr1:207462491 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.59-4035C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462491 | |||||||
chr1:207462554 | C | A | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-3972C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462554 | |||||||
chr1:207462850 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.59-3676A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462850 | |||||||
chr1:207462863 | G | T | 37 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0008 others(34): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.59-3663G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207462863 | |||||||
chr1:207463163 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG00544.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.59-3363T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207463163 | |||||||
chr1:207463264 | A | G | 1 | a0001c0003t0001g0041 | 2 | NA18960.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.59-3262A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207463264 | |||||||
chr1:207463330 | G | T | 2 | a0003c0006t0001g0052 a0007c0012t0003g0054 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-3196G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207463330 | |||||||
chr1:207464014 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.59-2512T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464014 | |||||||
chr1:207464106 | T | C | 1 | a0002c0002t0002g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-2420T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464106 | |||||||
chr1:207464175 | C | T | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.59-2351C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464175 | |||||||
chr1:207464336 | T | A | 1 | a0001c0003t0003g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.59-2190T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464336 | |||||||
chr1:207464384 | G | A | 1 | a0002c0005t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59-2142G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464384 | |||||||
chr1:207464549 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.59-1977A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464549 | |||||||
chr1:207464772 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0138 |
2 | HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.59-1754T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464772 | |||||||
chr1:207464785 | G | C | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.59-1741G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464785 | |||||||
chr1:207464970 | G | A | 1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-1556G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464970 | |||||||
chr1:207464992 | G | A | 1 | a0023c0020t0001g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.59-1534G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207464992 | |||||||
chr1:207465055 | C | T | 1 | a0003c0006t0001g0021 | 3 | HG03195.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.59-1471C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207465055 | |||||||
chr1:207465168 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0217 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.59-1358G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207465168 | |||||||
chr1:207465391 | T | C | 1 | a0002c0005t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.59-1135T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207465391 | |||||||
chr1:207465408 | C | CAT | 20 | a0002c0002t0002g0001 a0002c0002t0002g0008 a0002c0002t0002g0012 others(17): Show |
35 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.59-1104_59-1103dup others(2): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207465408 | ||||||
chr1:207465408 | CAT | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.59-1104_59-1103del others(2): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 207465408 | ||||||
chr1:207465421 | A | T | 3 | a0003c0006t0001g0052 a0007c0012t0003g0054 a0017c0024t0001g0053 |
3 | HG02040.hp2 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.59-1105A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207465421 | |||||||
chr1:207465501 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.59-1025G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207465501 | |||||||
chr1:207466060 | G | A | 1 | a0001c0003t0001g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-466G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207466060 | |||||||
chr1:207466350 | C | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
262 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.59-176C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207466350 | |||||||
chr1:207466518 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0035 |
4 | NA18989.hp1 NA18993.hp1 NA19070.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.59-8C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 1/19 | chr1 | 207466518 | |||||||
chr1:207466972 | C | T | 1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+60C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207466972 | |||||||
chr1:207467000 | G | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.445+88G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467000 | |||||||
chr1:207467135 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.445+223T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467135 | |||||||
chr1:207467147 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.445+235C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467147 | |||||||
chr1:207467328 | A | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.445+416A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467328 | |||||||
chr1:207467678 | T | C | 72 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(69): Show |
105 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.445+766T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467678 | |||||||
chr1:207467683 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.445+771G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467683 | |||||||
chr1:207467718 | C | T | 1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+806C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467718 | |||||||
chr1:207467878 | G | C | 8 | a0001c0001t0001g0028 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
9 | HG01884.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-649G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467878 | |||||||
chr1:207467984 | TTAAG | T | 5 | a0003c0006t0001g0021 a0003c0006t0001g0044 a0003c0006t0001g0221 others(2): Show |
10 | HG02451.hp1 HG02809.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-542_446-539del others(4): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467984 | |||||||
chr1:207467990 | A | T | 5 | a0003c0006t0001g0021 a0003c0006t0001g0044 a0003c0006t0001g0221 others(2): Show |
10 | HG02451.hp1 HG02809.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-537A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207467990 | |||||||
chr1:207468340 | AT | A | 6 | a0002c0002t0002g0045 a0002c0004t0001g0224 a0002c0004t0001g0225 others(3): Show |
7 | HG01109.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-177delT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 207468340 | ||||||
chr1:207468456 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.446-71A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207468456 | |||||||
chr1:207468495 | C | T | 37 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0008 others(34): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.446-32C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 2/19 | chr1 | 207468495 | |||||||
chr1:207468950 | G | A | 47 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0008 others(44): Show |
72 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.734+51G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 4/19 | chr1 | 207468950 | |||||||
chr1:207469503 | C | A | 1 | a0002c0002t0002g0045 | 2 | HG01109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.818-192C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 5/19 | chr1 | 207469503 | |||||||
chr1:207469625 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.818-70G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 5/19 | chr1 | 207469625 | |||||||
chr1:207469656 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.818-39C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 5/19 | chr1 | 207469656 | |||||||
chr1:207470202 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1225+100T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470202 | |||||||
chr1:207470221 | T | C | 4 | a0001c0003t0001g0027 a0001c0003t0001g0265 a0001c0003t0001g0266 others(1): Show |
5 | HG01243.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225+119T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470221 | |||||||
chr1:207470245 | G | A | 2 | a0003c0006t0001g0052 a0007c0012t0003g0054 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1225+143G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470245 | |||||||
chr1:207470264 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1225+162C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470264 | |||||||
chr1:207470328 | T | C | 68 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(65): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1225+226T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470328 | |||||||
chr1:207470370 | G | A | 1 | a0002c0002t0001g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1225+268G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470370 | |||||||
chr1:207470456 | A | T | 1 | a0001c0003t0001g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1226-284A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470456 | |||||||
chr1:207470604 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1226-136G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 6/19 | chr1 | 207470604 | |||||||
chr1:207471227 | A | G | 1 | a0002c0004t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1493+140A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 8/19 | chr1 | 207471227 | |||||||
chr1:207471744 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0088 others(5): Show |
10 | HG00621.hp1 HG01081.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1570+245C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207471744 | |||||||
chr1:207471916 | G | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA19063.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1570+417G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207471916 | |||||||
chr1:207471937 | G | C | 68 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(65): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1570+438G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207471937 | |||||||
chr1:207471970 | C | G | 1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1570+471C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207471970 | |||||||
chr1:207472016 | G | A | 9 | a0002c0005t0001g0022 a0002c0005t0001g0049 a0002c0005t0001g0050 others(6): Show |
13 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1570+517G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472016 | |||||||
chr1:207472040 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1570+541G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472040 | |||||||
chr1:207472114 | T | G | 1 | a0002c0005t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1570+615T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472114 | |||||||
chr1:207472218 | C | A | 2 | a0003c0006t0001g0021 a0007c0012t0001g0222 |
4 | HG03041.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-554C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472218 | |||||||
chr1:207472247 | T | G | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1571-525T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472247 | |||||||
chr1:207472334 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1571-438T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472334 | |||||||
chr1:207472398 | G | C | 68 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(65): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1571-374G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472398 | |||||||
chr1:207472494 | G | T | 2 | a0008c0011t0003g0042 a0008c0011t0003g0153 |
3 | NA18940.hp2 NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1571-278G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472494 | |||||||
chr1:207472512 | G | A | 1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1571-260G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472512 | |||||||
chr1:207472550 | G | A | 68 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(65): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1571-222G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472550 | |||||||
chr1:207472611 | C | A | 70 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(67): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1571-161C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472611 | |||||||
chr1:207472639 | C | A | 2 | a0001c0003t0001g0188 a0001c0003t0001g0189 |
2 | NA18977.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1571-133C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472639 | |||||||
chr1:207472764 | C | A | 1 | a0002c0002t0002g0242 | 1 | NA19012.hp1 | splice_region_variant&intron_variant | LOW | c.1571-8C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 9/19 | chr1 | 207472764 | |||||||
chr1:207473246 | C | T | 1 | a0003c0006t0001g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1978+67C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/19 | chr1 | 207473246 | |||||||
chr1:207473303 | A | G | 2 | a0003c0006t0001g0044 a0003c0006t0001g0221 |
3 | HG02809.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1978+124A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/19 | chr1 | 207473303 | |||||||
chr1:207473379 | A | G | 1 | a0003c0006t0003g0020 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1979-166A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/19 | chr1 | 207473379 | |||||||
chr1:207473492 | T | C | 1 | a0001c0001t0003g0156 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1979-53T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 10/19 | chr1 | 207473492 | |||||||
chr1:207473994 | A | G | 17 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(14): Show |
28 | HG01891.hp2 HG02040.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2240+109A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 12/19 | chr1 | 207473994 | |||||||
chr1:207474078 | A | T | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2241-163A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 12/19 | chr1 | 207474078 | |||||||
chr1:207474097 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2241-144T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 12/19 | chr1 | 207474097 | |||||||
chr1:207474199 | A | T | 2 | a0001c0001t0001g0116 a0001c0001t0007g0115 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2241-42A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 12/19 | chr1 | 207474199 | |||||||
chr1:207474648 | C | A | 16 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(13): Show |
27 | HG01891.hp2 HG02040.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.2324-176C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 13/19 | chr1 | 207474648 | |||||||
chr1:207475375 | ATTGT | A | 5 | a0002c0004t0001g0224 a0002c0004t0001g0225 a0002c0004t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2716+166_2716+169d others(6): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 207475375 | ||||||
chr1:207475458 | G | A | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2716+242G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | chr1 | 207475458 | |||||||
chr1:207475532 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2716+316A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | chr1 | 207475532 | |||||||
chr1:207475609 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2716+393A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | chr1 | 207475609 | |||||||
chr1:207475879 | G | A | 12 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(9): Show |
23 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2717-355G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | chr1 | 207475879 | |||||||
chr1:207475901 | A | G | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2717-333A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | chr1 | 207475901 | |||||||
chr1:207476089 | G | C | 2 | a0001c0003t0001g0027 a0021c0030t0001g0062 |
3 | HG01243.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2717-145G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 14/19 | chr1 | 207476089 | |||||||
chr1:207476563 | T | C | 1 | a0014c0028t0001g0163 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2902+144T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207476563 | |||||||
chr1:207476740 | A | G | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2902+321A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207476740 | |||||||
chr1:207476846 | A | G | 7 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(4): Show |
13 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2902+427A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207476846 | |||||||
chr1:207477119 | A | C | 12 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(9): Show |
23 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2902+700A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477119 | |||||||
chr1:207477153 | T | G | 1 | a0007c0012t0001g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2903-732T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477153 | |||||||
chr1:207477270 | G | A | 3 | a0003c0006t0001g0044 a0003c0006t0001g0221 a0003c0006t0003g0020 |
6 | HG02451.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2903-615G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477270 | |||||||
chr1:207477362 | A | G | 1 | a0009c0023t0001g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2903-523A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477362 | |||||||
chr1:207477395 | C | T | 1 | a0002c0004t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2903-490C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477395 | |||||||
chr1:207477444 | C | A | 1 | a0023c0020t0001g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2903-441C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477444 | |||||||
chr1:207477512 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2903-373G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477512 | |||||||
chr1:207477593 | G | T | 15 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0026 others(12): Show |
17 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.2903-292G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477593 | |||||||
chr1:207477678 | G | C | 1 | a0003c0006t0001g0021 | 3 | HG03195.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2903-207G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477678 | |||||||
chr1:207477714 | T | C | 4 | a0002c0004t0001g0026 a0002c0004t0001g0055 a0002c0004t0001g0058 others(1): Show |
5 | HG00140.hp1 HG01168.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2903-171T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 15/19 | chr1 | 207477714 | |||||||
chr1:207478140 | G | A | 2 | a0001c0003t0001g0180 a0001c0003t0001g0185 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3088+70G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478140 | |||||||
chr1:207478141 | C | T | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3088+71C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478141 | |||||||
chr1:207478368 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3088+298A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478368 | |||||||
chr1:207478371 | T | A | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3088+301T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478371 | |||||||
chr1:207478383 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0171 |
2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3088+313C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478383 | |||||||
chr1:207478490 | C | A | 74 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(71): Show |
112 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3088+420C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478490 | |||||||
chr1:207478525 | C | CA | 23 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0073 others(20): Show |
27 | HG00621.hp2 HG01109.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.3088+477dupA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478525 | ||||||
chr1:207478525 | CA | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0037 others(34): Show |
43 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.3088+477delA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478525 | ||||||
chr1:207478525 | CAA | C | 46 | a0001c0001t0001g0127 a0001c0001t0001g0178 a0002c0002t0002g0001 others(43): Show |
72 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.3088+476_3088+477d others(4): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478525 | ||||||
chr1:207478525 | CAAA | C | 26 | a0002c0002t0001g0013 a0002c0002t0001g0023 a0002c0002t0001g0051 others(23): Show |
37 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.3088+475_3088+477d others(5): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478525 | ||||||
chr1:207478525 | CAAAAAAA others(4): Show |
C | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3088+467_3088+477d others(13): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478525 | ||||||
chr1:207478544 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0075 |
2 | HG04199.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.3088+474A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478544 | |||||||
chr1:207478590 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.3088+520A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478590 | |||||||
chr1:207478612 | T | A | 1 | a0002c0005t0001g0049 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3088+542T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478612 | |||||||
chr1:207478718 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3089-539G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478718 | |||||||
chr1:207478831 | A | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0037 others(37): Show |
48 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3089-426A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478831 | |||||||
chr1:207478874 | A | G | 1 | a0002c0005t0001g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3089-383A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207478874 | |||||||
chr1:207478887 | G | GA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0072 others(10): Show |
15 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.3089-361dupA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478887 | ||||||
chr1:207478968 | TTTTTTG | T | 83 | a0001c0003t0001g0027 a0001c0003t0001g0265 a0001c0003t0001g0266 others(80): Show |
122 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.3089-260_3089-255d others(8): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 207478968 | ||||||
chr1:207479203 | T | C | 8 | a0001c0003t0001g0041 a0001c0003t0001g0190 a0001c0003t0001g0191 others(5): Show |
9 | HG01433.hp2 NA18954.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.3089-54T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 16/19 | chr1 | 207479203 | |||||||
chr1:207479352 | A | G | 1 | a0011c0025t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3112+72A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479352 | |||||||
chr1:207479430 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3112+150C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479430 | |||||||
chr1:207479466 | A | G | 2 | a0001c0003t0001g0191 a0001c0003t0004g0200 |
2 | HG01433.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3112+186A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479466 | |||||||
chr1:207479482 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3112+202C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479482 | |||||||
chr1:207479499 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0119 a0001c0001t0001g0137 others(1): Show |
6 | HG01081.hp2 HG01256.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+219T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479499 | |||||||
chr1:207479583 | A | C | 4 | a0003c0006t0001g0052 a0007c0012t0001g0223 a0007c0012t0003g0054 others(1): Show |
4 | HG02040.hp2 HG02109.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3112+303A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479583 | |||||||
chr1:207479589 | C | T | 5 | a0003c0006t0001g0052 a0007c0012t0001g0223 a0007c0012t0003g0054 others(2): Show |
5 | HG02040.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3112+309C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479589 | |||||||
chr1:207479642 | T | G | 8 | a0001c0003t0003g0211 a0002c0002t0001g0013 a0002c0002t0001g0023 others(5): Show |
14 | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3113-336T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479642 | |||||||
chr1:207479647 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.3113-331A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479647 | |||||||
chr1:207479660 | T | C | 2 | a0002c0004t0001g0025 a0022c0019t0001g0025 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3113-318T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479660 | |||||||
chr1:207479761 | A | C | 54 | a0001c0003t0001g0266 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
77 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.3113-217A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479761 | |||||||
chr1:207479833 | C | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(92): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.3113-145C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 17/19 | chr1 | 207479833 | |||||||
chr1:207480099 | T | A | 35 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0008 others(32): Show |
56 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.3188+46T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480099 | |||||||
chr1:207480239 | C | T | 1 | a0001c0003t0001g0212 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3188+186C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480239 | |||||||
chr1:207480356 | T | A | 18 | a0001c0001t0001g0142 a0001c0003t0001g0265 a0001c0003t0001g0266 others(15): Show |
20 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.3188+303T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480356 | |||||||
chr1:207480359 | G | A | 1 | a0003c0006t0003g0020 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3188+306G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480359 | |||||||
chr1:207480446 | A | G | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3188+393A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480446 | |||||||
chr1:207480448 | G | GT | 44 | a0001c0003t0001g0185 a0002c0002t0002g0001 a0002c0002t0002g0005 others(41): Show |
70 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.3188+395_3188+396i others(3): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480448 | |||||||
chr1:207480469 | T | C | 45 | a0001c0003t0001g0185 a0002c0002t0002g0001 a0002c0002t0002g0005 others(42): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.3188+416T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480469 | |||||||
chr1:207480648 | A | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0088 others(3): Show |
8 | HG01256.hp2 HG01952.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.3188+595A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480648 | |||||||
chr1:207480648 | A | T | 1 | a0001c0003t0001g0205 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3188+595A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480648 | |||||||
chr1:207480920 | CA | C | 46 | a0001c0003t0001g0185 a0002c0002t0002g0001 a0002c0002t0002g0005 others(43): Show |
70 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.3188+876delA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 207480920 | ||||||
chr1:207480956 | A | T | 19 | a0001c0001t0001g0142 a0001c0003t0001g0265 a0001c0003t0001g0266 others(16): Show |
21 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.3188+903A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207480956 | |||||||
chr1:207481026 | G | T | 1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3188+973G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207481026 | |||||||
chr1:207481226 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3188+1173T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207481226 | |||||||
chr1:207481535 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3188+1482G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207481535 | |||||||
chr1:207481848 | C | G | 37 | a0001c0001t0001g0113 a0001c0001t0001g0165 a0002c0002t0002g0001 others(34): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.3188+1795C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207481848 | |||||||
chr1:207482127 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
132 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.3188+2074A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482127 | |||||||
chr1:207482262 | T | C | 1 | a0002c0002t0002g0243 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3188+2209T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482262 | |||||||
chr1:207482454 | G | T | 1 | a0002c0002t0002g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3188+2401G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482454 | |||||||
chr1:207482470 | G | A | 37 | a0001c0001t0001g0113 a0001c0001t0001g0165 a0002c0002t0002g0001 others(34): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.3188+2417G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482470 | |||||||
chr1:207482485 | C | T | 1 | a0003c0006t0001g0021 | 3 | HG03195.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3188+2432C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482485 | |||||||
chr1:207482527 | C | T | 1 | a0003c0006t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3188+2474C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482527 | |||||||
chr1:207482705 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.3188+2652C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482705 | |||||||
chr1:207482903 | T | G | 1 | a0017c0024t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3189-2561T>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207482903 | |||||||
chr1:207482960 | GA | G | 58 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0063 others(55): Show |
71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.3189-2490delA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 207482960 | ||||||
chr1:207483018 | T | C | 1 | a0007c0012t0003g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3189-2446T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483018 | |||||||
chr1:207483069 | G | A | 5 | a0002c0002t0002g0246 a0002c0002t0002g0250 a0003c0006t0001g0044 others(2): Show |
6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3189-2395G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483069 | |||||||
chr1:207483105 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3189-2359C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483105 | |||||||
chr1:207483117 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3189-2347C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483117 | |||||||
chr1:207483144 | T | A | 1 | a0003c0006t0001g0021 | 3 | HG03195.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3189-2320T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483144 | |||||||
chr1:207483157 | C | T | 37 | a0001c0001t0001g0113 a0001c0001t0001g0165 a0002c0002t0002g0001 others(34): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.3189-2307C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483157 | |||||||
chr1:207483243 | C | T | 5 | a0001c0007t0001g0195 a0001c0007t0001g0207 a0001c0007t0003g0187 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3189-2221C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483243 | |||||||
chr1:207483260 | G | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.3189-2204G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483260 | |||||||
chr1:207483313 | T | A | 1 | a0001c0003t0001g0204 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3189-2151T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483313 | |||||||
chr1:207483352 | G | C | 1 | a0021c0030t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3189-2112G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483352 | |||||||
chr1:207483555 | G | GT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.3189-1900dupT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 207483555 | ||||||
chr1:207483555 | G | GTT | 10 | a0001c0003t0001g0185 a0001c0003t0001g0265 a0001c0003t0003g0211 others(7): Show |
10 | HG01109.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3189-1901_3189-190 others(6): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 207483555 | ||||||
chr1:207483828 | C | A | 17 | a0001c0001t0001g0142 a0001c0003t0001g0266 a0001c0007t0001g0196 others(14): Show |
22 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.3189-1636C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483828 | |||||||
chr1:207483829 | G | A | 2 | a0007c0012t0001g0223 a0019c0021t0001g0260 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3189-1635G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207483829 | |||||||
chr1:207484030 | C | T | 39 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0064 others(36): Show |
43 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.3189-1434C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484030 | |||||||
chr1:207484178 | C | A | 1 | a0018c0018t0001g0255 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3189-1286C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484178 | |||||||
chr1:207484330 | TTTATTTC others(11): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3189-1133_3189-111 others(22): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484330 | |||||||
chr1:207484349 | C | A | 1 | a0002c0002t0002g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3189-1115C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484349 | |||||||
chr1:207484543 | C | T | 1 | a0005c0010t0002g0249 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3189-921C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484543 | |||||||
chr1:207484680 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.3189-784T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484680 | |||||||
chr1:207484800 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.3189-664A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484800 | |||||||
chr1:207484811 | A | T | 1 | a0001c0003t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3189-653A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484811 | |||||||
chr1:207484814 | C | T | 2 | a0001c0003t0001g0180 a0017c0024t0001g0053 |
2 | HG02040.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3189-650C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484814 | |||||||
chr1:207484946 | T | C | 1 | a0003c0006t0003g0020 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3189-518T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207484946 | |||||||
chr1:207485050 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0146 a0015c0017t0001g0014 |
4 | HG00280.hp1 HG00642.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3189-414C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207485050 | |||||||
chr1:207485162 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.3189-302A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207485162 | |||||||
chr1:207485286 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3189-178T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207485286 | |||||||
chr1:207485328 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3189-136A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | chr1 | 207485328 | |||||||
chr1:207485454 | TTC | T | 1 | a0003c0006t0003g0020 | 3 | HG02451.hp1 HG03579.hp2 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.3189-8_3189-7delCT | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 207485454 | ||||||
chr1:207485799 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*18+227C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207485799 | |||||||
chr1:207486124 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*18+552G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486124 | |||||||
chr1:207486184 | CTGCGCCA others(4): Show |
C | 1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*18+613_*18+623del others(11): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486184 | |||||||
chr1:207486188 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.*18+616G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486188 | |||||||
chr1:207486197 | C | A | 1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*18+625C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486197 | |||||||
chr1:207486199 | C | A | 1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*18+627C>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486199 | |||||||
chr1:207486200 | C | G | 1 | a0011c0026t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*18+628C>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486200 | |||||||
chr1:207486230 | C | CA | 33 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0061 others(30): Show |
42 | HG00621.hp1 HG01106.hp2 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.*18+684dupA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAA | 9 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0105 others(6): Show |
10 | HG00621.hp2 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.*18+683_*18+684dup others(2): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0064 a0001c0001t0001g0092 a0001c0001t0001g0126 others(4): Show |
7 | HG00558.hp1 HG00558.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.*18+676_*18+684dup others(9): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(3): Show |
14 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0098 others(11): Show |
15 | HG02040.hp1 HG02074.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.*18+675_*18+684dup others(10): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(4): Show |
12 | a0001c0001t0001g0037 a0001c0001t0001g0076 a0001c0001t0001g0088 others(9): Show |
15 | HG01891.hp2 HG02602.hp2 HG03130.hp2 others(12): Show |
intron_variant | MODIFIER | c.*18+674_*18+684dup others(11): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0267 a0001c0003t0001g0182 a0023c0020t0001g0057 |
3 | HG02698.hp2 HG03491.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.*18+673_*18+684dup others(12): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(6): Show |
2 | a0001c0003t0001g0181 a0001c0003t0005g0201 |
2 | HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.*18+672_*18+684dup others(13): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(7): Show |
1 | a0001c0007t0003g0187 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*18+671_*18+684dup others(14): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(8): Show |
3 | a0001c0007t0001g0195 a0001c0007t0001g0207 a0001c0007t0003g0194 |
3 | HG01891.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*18+670_*18+684dup others(15): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(9): Show |
11 | a0001c0001t0001g0110 a0001c0001t0001g0117 a0001c0003t0001g0040 others(8): Show |
13 | HG01433.hp2 HG02055.hp2 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.*18+669_*18+684dup others(16): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(10): Show |
12 | a0001c0001t0001g0030 a0001c0001t0001g0085 a0001c0001t0001g0122 others(9): Show |
14 | HG00544.hp2 HG02083.hp2 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.*18+668_*18+684dup others(17): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0108 |
2 | NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.*18+667_*18+684dup others(18): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(13): Show |
2 | a0001c0003t0001g0041 a0001c0003t0001g0197 |
3 | NA18960.hp2 NA18988.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.*18+665_*18+684dup others(20): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | C | CAAAAAAA others(14): Show |
2 | a0001c0003t0001g0208 a0001c0003t0004g0200 |
2 | NA18979.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.*18+664_*18+684dup others(21): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | CA | C | 24 | a0001c0001t0001g0033 a0001c0001t0001g0103 a0001c0001t0001g0107 others(21): Show |
35 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.*18+684delA | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | CAAA | C | 5 | a0001c0001t0001g0142 a0002c0004t0001g0026 a0002c0004t0001g0055 others(2): Show |
6 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.*18+682_*18+684del others(3): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486230 | CAAAAA | C | 22 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0111 others(19): Show |
29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.*18+680_*18+684del others(5): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486230 | ||||||
chr1:207486272 | A | G | 2 | a0002c0002t0001g0023 a0002c0002t0001g0051 |
5 | HG01891.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.*18+700A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486272 | |||||||
chr1:207486346 | G | A | 11 | a0001c0003t0001g0266 a0001c0007t0001g0196 a0002c0002t0001g0013 others(8): Show |
15 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.*18+774G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486346 | |||||||
chr1:207486452 | G | A | 1 | a0002c0002t0002g0241 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*18+880G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486452 | |||||||
chr1:207486568 | CTG | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.*18+1000_*18+1001d others(4): Show |
CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 207486568 | ||||||
chr1:207486721 | G | A | 4 | a0001c0001t0001g0215 a0001c0003t0001g0027 a0007c0012t0001g0222 others(1): Show |
5 | HG01243.hp1 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.*18+1149G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486721 | |||||||
chr1:207486726 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.*18+1154C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486726 | |||||||
chr1:207486778 | C | T | 2 | a0002c0002t0002g0047 a0002c0002t0002g0237 |
3 | HG01255.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.*18+1206C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486778 | |||||||
chr1:207486779 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.*18+1207G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486779 | |||||||
chr1:207486978 | T | C | 2 | a0002c0002t0002g0246 a0002c0002t0002g0250 |
2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.*18+1406T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486978 | |||||||
chr1:207486999 | T | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.*18+1427T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207486999 | |||||||
chr1:207487031 | C | T | 1 | a0024c0032t0001g0109 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.*18+1459C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487031 | |||||||
chr1:207487033 | A | G | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.*18+1461A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487033 | |||||||
chr1:207487038 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.*18+1466T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487038 | |||||||
chr1:207487041 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.*18+1469A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487041 | |||||||
chr1:207487045 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.*18+1473G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487045 | |||||||
chr1:207487313 | G | A | 1 | a0001c0001t0007g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.*18+1741G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487313 | |||||||
chr1:207487458 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.*19-1684T>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487458 | |||||||
chr1:207487520 | A | C | 5 | a0002c0002t0002g0008 a0002c0002t0002g0229 a0002c0002t0002g0230 others(2): Show |
9 | HG00423.hp2 NA18947.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.*19-1622A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487520 | |||||||
chr1:207487573 | T | C | 7 | a0002c0002t0002g0246 a0002c0002t0002g0250 a0002c0004t0001g0224 others(4): Show |
7 | HG02717.hp1 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.*19-1569T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487573 | |||||||
chr1:207487610 | G | A | 1 | a0007c0012t0003g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*19-1532G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487610 | |||||||
chr1:207487619 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.*19-1523A>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487619 | |||||||
chr1:207487756 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.*19-1386G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487756 | |||||||
chr1:207487794 | C | T | 7 | a0002c0002t0002g0246 a0002c0002t0002g0250 a0002c0004t0001g0224 others(4): Show |
7 | HG02717.hp1 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.*19-1348C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487794 | |||||||
chr1:207487944 | G | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.*19-1198G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487944 | |||||||
chr1:207487976 | G | A | 1 | a0001c0016t0003g0186 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.*19-1166G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207487976 | |||||||
chr1:207488053 | G | A | 8 | a0002c0002t0001g0013 a0002c0002t0001g0262 a0002c0004t0001g0025 others(5): Show |
11 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.*19-1089G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488053 | |||||||
chr1:207488101 | A | G | 8 | a0001c0001t0001g0142 a0001c0003t0001g0185 a0002c0004t0001g0026 others(5): Show |
9 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.*19-1041A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488101 | |||||||
chr1:207488140 | A | G | 11 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0111 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.*19-1002A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488140 | |||||||
chr1:207488170 | A | T | 1 | a0001c0003t0003g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*19-972A>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488170 | |||||||
chr1:207488192 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.*19-950G>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488192 | |||||||
chr1:207488205 | G | C | 1 | a0001c0001t0001g0176 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.*19-937G>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488205 | |||||||
chr1:207488207 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.*19-935T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488207 | |||||||
chr1:207488292 | A | G | 5 | a0002c0004t0001g0224 a0002c0004t0001g0225 a0002c0004t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.*19-850A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488292 | |||||||
chr1:207488295 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.*19-847C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488295 | |||||||
chr1:207488334 | T | C | 5 | a0001c0001t0001g0142 a0002c0004t0001g0026 a0002c0004t0001g0055 others(2): Show |
6 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.*19-808T>C | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488334 | |||||||
chr1:207488516 | C | T | 11 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0111 others(8): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.*19-626C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488516 | |||||||
chr1:207488610 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*19-532G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488610 | |||||||
chr1:207488835 | A | G | 31 | a0001c0001t0001g0037 a0001c0001t0001g0064 a0001c0001t0001g0076 others(28): Show |
32 | HG00558.hp1 HG00558.hp2 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.*19-307A>G | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488835 | |||||||
chr1:207488961 | G | A | 4 | a0001c0003t0001g0266 a0001c0007t0001g0196 a0002c0004t0001g0024 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.*19-181G>A | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207488961 | |||||||
chr1:207489087 | C | T | 3 | a0002c0004t0001g0025 a0002c0004t0001g0056 a0022c0019t0001g0025 |
3 | HG02622.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*19-55C>T | CR2 | ENSG00000117322.19 | transcript | ENST00000367057.8 | protein_coding | 19/19 | chr1 | 207489087 |