Item | Value |
---|---|
geneid | 9398 |
ensemblid | ENSG00000134256.13 |
hgncid | 5949 |
symbol | CD101 |
name | CD101 molecule |
refseq_nuc | NM_001256106.3 |
refseq_prot | NP_001243035.1 |
ensembl_nuc | ENST00000682167.1 |
ensembl_prot | ENSP00000508039.1 |
mane_status | MANE Select |
chr | chr1 |
start | 117001760 |
end | 117036552 |
strand | + |
ver | v1.2 |
region | chr1:117001760-117036552 |
region5000 | chr1:116996760-117041552 |
regionname0 | CD101_chr1_117001760_117036552 |
regionname5000 | CD101_chr1_116996760_117041552 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1021 | 264 | 58 | 41 | 131 | 6 | 28 | 99 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0002 | 0/1 | 1021 | 52 | 6 | 19 | 14 | 6 | 6 | 11 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0003 | 1/0 | 1021 | 34 | 2 | 3 | 25 | 1 | 2 | 18 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0004 | 0/0 | 1021 | 14 | 0 | 0 | 14 | 0 | 0 | 12 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0005 | 0/0 | 1021 | 10 | 4 | 4 | 0 | 1 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0006 | 0/0 | 1021 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0007 | 0/0 | 1021 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0008 | 0/0 | 1021 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0009 | 0/0 | 1021 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0010 | 0/0 | 1021 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0011 | 0/0 | 1021 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0012 | 0/0 | 1021 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0013 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0014 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0015 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0016 | 0/0 | 1021 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0017 | 0/0 | 1021 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0018 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0019 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0020 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0021 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0022 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0023 | 0/0 | 1011 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1006): Show |
chr1 | 116996760 | 117041552 |
a0024 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0025 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0026 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0027 | 0/0 | 1021 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0028 | 0/0 | 1021 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
a0029 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | MAGIS others(1016): Show |
chr1 | 116996760 | 117041552 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3063 | 105 | 46 | 18 | 31 | 3 | 7 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0002 | 0/0 | 3063 | 75 | 1 | 20 | 38 | 3 | 13 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0003 | 0/0 | 3063 | 75 | 4 | 3 | 61 | 0 | 7 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0010 | 0/0 | 3063 | 4 | 4 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0022 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0031 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0033 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0034 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0001c0038 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0002c0004 | 0/1 | 3063 | 51 | 6 | 19 | 13 | 6 | 6 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0002c0040 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0003c0005 | 1/0 | 3063 | 34 | 2 | 3 | 25 | 1 | 2 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0004c0006 | 0/0 | 3063 | 14 | 0 | 0 | 14 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0005c0007 | 0/0 | 3063 | 10 | 4 | 4 | 0 | 1 | 1 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0006c0008 | 0/0 | 3063 | 5 | 5 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0006c0021 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0007c0012 | 0/0 | 3063 | 3 | 0 | 2 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0007c0020 | 0/0 | 3063 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0007c0036 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0008c0009 | 0/0 | 3063 | 5 | 0 | 4 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0009c0011 | 0/0 | 3063 | 4 | 4 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0010c0013 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0010c0030 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0011c0016 | 0/0 | 3063 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0011c0026 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0012c0014 | 0/0 | 3063 | 2 | 1 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0013c0015 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0014c0023 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0014c0029 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0015c0019 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0016c0018 | 0/0 | 3063 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0017c0017 | 0/0 | 3063 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0018c0039 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0019c0037 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0020c0024 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0021c0028 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0022c0043 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0023c0041 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3028): Show |
chr1 | 116996760 | 117041552 | ||
a0024c0027 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0025c0025 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0026c0032 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0027c0042 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0028c0035 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 | ||
a0029c0044 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ATGGC others(3058): Show |
chr1 | 116996760 | 117041552 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3542 | 87 | 31 | 18 | 29 | 2 | 7 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0001t0002 | 0/0 | 3541 | 6 | 4 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0001c0001t0003 | 0/0 | 3543 | 7 | 6 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0001c0001t0004 | 0/0 | 3541 | 5 | 5 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0001c0002t0001 | 0/0 | 3542 | 65 | 1 | 20 | 29 | 2 | 13 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0002t0002 | 0/0 | 3541 | 8 | 0 | 0 | 7 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0001c0002t0003 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0001c0002t0007 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0003t0001 | 0/0 | 3542 | 68 | 3 | 3 | 55 | 0 | 7 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0003t0002 | 0/0 | 3541 | 6 | 0 | 0 | 6 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0001c0003t0004 | 0/0 | 3541 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0001c0010t0003 | 0/0 | 3543 | 4 | 4 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0001c0022t0001 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0031t0006 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0033t0001 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0001c0034t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0001c0038t0001 | 0/0 | 3542 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0002c0004t0001 | 0/1 | 3542 | 46 | 1 | 19 | 13 | 6 | 6 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0002c0004t0002 | 0/0 | 3541 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0002c0004t0003 | 0/0 | 3543 | 3 | 3 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0002c0040t0001 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0003c0005t0001 | 1/0 | 3542 | 28 | 2 | 1 | 22 | 1 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0003c0005t0002 | 0/0 | 3541 | 6 | 0 | 2 | 3 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0004c0006t0001 | 0/0 | 3542 | 13 | 0 | 0 | 13 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0004c0006t0002 | 0/0 | 3541 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0005c0007t0001 | 0/0 | 3542 | 9 | 3 | 4 | 0 | 1 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0005c0007t0004 | 0/0 | 3541 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0006c0008t0001 | 0/0 | 3542 | 5 | 5 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0006c0021t0001 | 0/0 | 3542 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0007c0012t0001 | 0/0 | 3542 | 3 | 0 | 2 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0007c0020t0001 | 0/0 | 3542 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0007c0036t0001 | 0/0 | 3542 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0008c0009t0001 | 0/0 | 3542 | 5 | 0 | 4 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0009c0011t0001 | 0/0 | 3542 | 4 | 4 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0010c0013t0004 | 0/0 | 3541 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0010c0030t0004 | 0/0 | 3541 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0011c0016t0001 | 0/0 | 3542 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0011c0026t0001 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0012c0014t0001 | 0/0 | 3542 | 2 | 1 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0013c0015t0001 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0013c0015t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0014c0023t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0014c0029t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0015c0019t0001 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0015c0019t0002 | 0/0 | 3541 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0016c0018t0001 | 0/0 | 3542 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0017c0017t0001 | 0/0 | 3542 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0018c0039t0001 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0019c0037t0001 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0020c0024t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0021c0028t0001 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0022c0043t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0023c0041t0005 | 0/0 | 3509 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3504): Show |
chr1 | 116996760 | 117041552 |
a0024c0027t0001 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0025c0025t0003 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3538): Show |
chr1 | 116996760 | 117041552 |
a0026c0032t0002 | 0/0 | 3541 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3536): Show |
chr1 | 116996760 | 117041552 |
a0027c0042t0001 | 0/0 | 3542 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0028c0035t0001 | 0/0 | 3542 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
a0029c0044t0001 | 0/0 | 3542 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | ACTCA others(3537): Show |
chr1 | 116996760 | 117041552 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0002t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0003t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0010t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0010t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0010t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0010t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0022t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0031t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0033t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0034t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0001c0038t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0001 | 0/0 | 8 | 1 | 4 | 0 | 1 | 2 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0004t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0002c0040t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0013 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0003c0005t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0004c0006t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0005c0007t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0006c0008t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0006c0008t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0006c0008t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0006c0008t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0006c0021t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0006c0021t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0007c0012t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0007c0012t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0007c0020t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0007c0020t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0007c0036t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0008c0009t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0008c0009t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0008c0009t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0008c0009t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0009c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0009c0011t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0009c0011t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0009c0011t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0010c0013t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0010c0013t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0010c0030t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0011c0016t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0011c0016t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0011c0026t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0012c0014t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0012c0014t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0013c0015t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0013c0015t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0014c0023t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0014c0029t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0015c0019t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0015c0019t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0016c0018t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0016c0018t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0017c0017t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0017c0017t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0018c0039t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0019c0037t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0020c0024t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0021c0028t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0022c0043t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0023c0041t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0024c0027t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0025c0025t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0026c0032t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0027c0042t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0028c0035t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
a0029c0044t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | GBR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0095 | EUR | GBR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00140 | hp1 | a0008 | c0009 | t0001 | g0079 | EUR | GBR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00140 | hp2 | a0002 | c0004 | t0001 | g0044 | EUR | GBR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0203 | EUR | FIN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00280 | hp2 | a0003 | c0005 | t0001 | g0325 | EUR | FIN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00323 | hp1 | a0002 | c0004 | t0001 | g0224 | EUR | FIN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | FIN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00408 | hp2 | a0018 | c0039 | t0001 | g0254 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00438 | hp2 | a0003 | c0005 | t0002 | g0276 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00621 | hp1 | a0003 | c0005 | t0001 | g0268 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00639 | hp2 | a0002 | c0004 | t0001 | g0001 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0336 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | CHS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00733 | hp1 | a0002 | c0004 | t0001 | g0044 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00741 | hp1 | a0005 | c0007 | t0001 | g0014 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0046 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01070 | hp1 | a0002 | c0004 | t0001 | g0047 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0046 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01074 | hp1 | a0002 | c0004 | t0001 | g0047 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01081 | hp2 | a0002 | c0004 | t0001 | g0136 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01109 | hp1 | a0005 | c0007 | t0001 | g0328 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01167 | hp1 | a0002 | c0004 | t0001 | g0292 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01167 | hp2 | a0008 | c0009 | t0001 | g0016 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01168 | hp1 | a0007 | c0012 | t0001 | g0051 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01168 | hp2 | a0002 | c0004 | t0001 | g0281 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01169 | hp1 | a0008 | c0009 | t0001 | g0016 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01169 | hp2 | a0007 | c0012 | t0001 | g0051 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01175 | hp2 | a0003 | c0005 | t0001 | g0013 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01192 | hp1 | a0002 | c0004 | t0001 | g0231 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01192 | hp2 | a0005 | c0007 | t0001 | g0014 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01255 | hp1 | a0005 | c0007 | t0001 | g0329 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01258 | hp1 | a0002 | c0004 | t0001 | g0303 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01261 | hp1 | a0002 | c0004 | t0001 | g0290 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01346 | hp1 | a0002 | c0004 | t0001 | g0280 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01358 | hp2 | a0002 | c0004 | t0001 | g0001 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01361 | hp1 | a0002 | c0004 | t0001 | g0244 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01361 | hp2 | a0002 | c0004 | t0001 | g0138 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01433 | hp1 | a0002 | c0004 | t0001 | g0001 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01433 | hp2 | a0012 | c0014 | t0001 | g0342 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01496 | hp1 | a0002 | c0004 | t0001 | g0001 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01515 | hp1 | a0005 | c0007 | t0001 | g0330 | EUR | IBS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01515 | hp2 | a0002 | c0004 | t0001 | g0235 | EUR | IBS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01516 | hp1 | a0007 | c0012 | t0001 | g0189 | EUR | IBS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01516 | hp2 | a0002 | c0004 | t0001 | g0234 | EUR | IBS | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01884 | hp2 | a0005 | c0007 | t0004 | g0326 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01891 | hp1 | a0006 | c0021 | t0001 | g0116 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0146 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01943 | hp2 | a0008 | c0009 | t0001 | g0017 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0161 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02015 | hp1 | a0003 | c0005 | t0001 | g0271 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02040 | hp2 | a0001 | c0003 | t0002 | g0174 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02055 | hp2 | a0001 | c0031 | t0006 | g0240 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02056 | hp1 | a0004 | c0006 | t0001 | g0040 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0335 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02071 | hp1 | a0003 | c0005 | t0001 | g0298 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02074 | hp1 | a0003 | c0005 | t0001 | g0266 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02083 | hp1 | a0004 | c0006 | t0002 | g0255 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02129 | hp1 | a0003 | c0005 | t0001 | g0295 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02129 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02132 | hp1 | a0003 | c0005 | t0002 | g0267 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02132 | hp2 | a0002 | c0040 | t0001 | g0310 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02135 | hp2 | a0002 | c0004 | t0001 | g0038 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0338 | EAS | CDX | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | CDX | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02165 | hp1 | a0019 | c0037 | t0001 | g0108 | EAS | CDX | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0337 | EAS | CDX | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02257 | hp1 | a0020 | c0024 | t0003 | g0332 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02258 | hp1 | a0003 | c0005 | t0001 | g0013 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02273 | hp1 | a0003 | c0005 | t0002 | g0035 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02280 | hp1 | a0001 | c0010 | t0003 | g0124 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02280 | hp2 | a0014 | c0029 | t0003 | g0262 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02293 | hp1 | a0003 | c0005 | t0002 | g0035 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02293 | hp2 | a0008 | c0009 | t0001 | g0069 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02451 | hp1 | a0002 | c0004 | t0003 | g0307 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02523 | hp2 | a0001 | c0002 | t0007 | g0019 | EAS | KHV | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02615 | hp2 | a0002 | c0004 | t0002 | g0308 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02622 | hp2 | a0015 | c0019 | t0002 | g0134 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02630 | hp2 | a0009 | c0011 | t0001 | g0305 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02647 | hp1 | a0021 | c0028 | t0001 | g0288 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02647 | hp2 | a0022 | c0043 | t0003 | g0239 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02683 | hp2 | a0023 | c0041 | t0005 | g0243 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0147 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02698 | hp2 | a0002 | c0004 | t0001 | g0001 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02717 | hp1 | a0005 | c0007 | t0001 | g0052 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02717 | hp2 | a0012 | c0014 | t0001 | g0343 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02723 | hp1 | a0013 | c0015 | t0001 | g0122 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0229 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02738 | hp1 | a0002 | c0004 | t0001 | g0282 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02809 | hp2 | a0002 | c0004 | t0003 | g0048 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02818 | hp1 | a0024 | c0027 | t0001 | g0133 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02896 | hp2 | a0002 | c0004 | t0002 | g0309 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02922 | hp1 | a0025 | c0025 | t0003 | g0249 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02922 | hp2 | a0001 | c0010 | t0003 | g0128 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02965 | hp1 | a0001 | c0010 | t0003 | g0125 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02970 | hp1 | a0006 | c0008 | t0001 | g0340 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02970 | hp2 | a0001 | c0022 | t0001 | g0127 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03017 | hp2 | a0003 | c0005 | t0002 | g0316 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03041 | hp1 | a0001 | c0003 | t0004 | g0178 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03098 | hp1 | a0014 | c0023 | t0003 | g0130 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03098 | hp2 | a0005 | c0007 | t0001 | g0052 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03139 | hp2 | a0009 | c0011 | t0001 | g0252 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03195 | hp1 | a0006 | c0008 | t0001 | g0053 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03209 | hp2 | a0001 | c0034 | t0003 | g0162 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03239 | hp2 | a0002 | c0004 | t0001 | g0319 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03453 | hp1 | a0006 | c0008 | t0001 | g0341 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03486 | hp1 | a0026 | c0032 | t0002 | g0228 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03486 | hp2 | a0005 | c0007 | t0001 | g0327 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03491 | hp1 | a0011 | c0016 | t0001 | g0091 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03492 | hp1 | a0011 | c0016 | t0001 | g0092 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03516 | hp1 | a0003 | c0005 | t0001 | g0299 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03516 | hp2 | a0001 | c0010 | t0003 | g0123 | AFR | ESN | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03540 | hp2 | a0015 | c0019 | t0001 | g0135 | AFR | GWD | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03579 | hp2 | a0006 | c0008 | t0001 | g0053 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0131 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0132 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03688 | hp1 | a0001 | c0038 | t0001 | g0075 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03688 | hp2 | a0007 | c0036 | t0001 | g0143 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03704 | hp1 | a0007 | c0020 | t0001 | g0216 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03704 | hp2 | a0002 | c0004 | t0001 | g0318 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03710 | hp1 | a0005 | c0007 | t0001 | g0014 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03834 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03834 | hp2 | a0003 | c0005 | t0001 | g0311 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03927 | hp2 | a0016 | c0018 | t0001 | g0265 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03942 | hp2 | a0002 | c0004 | t0001 | g0291 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04115 | hp2 | a0016 | c0018 | t0001 | g0236 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0160 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04228 | hp1 | a0027 | c0042 | t0001 | g0279 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG04228 | hp2 | a0007 | c0020 | t0001 | g0003 | SAS | STU | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | CHB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18747 | hp2 | a0002 | c0004 | t0001 | g0012 | EAS | CHB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18906 | hp1 | a0009 | c0011 | t0001 | g0304 | AFR | YRI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18906 | hp2 | a0002 | c0004 | t0003 | g0048 | AFR | YRI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18939 | hp2 | a0003 | c0005 | t0001 | g0274 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18941 | hp2 | a0004 | c0006 | t0001 | g0039 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18942 | hp2 | a0003 | c0005 | t0001 | g0273 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18945 | hp1 | a0004 | c0006 | t0001 | g0039 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0027 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18949 | hp2 | a0003 | c0005 | t0001 | g0277 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18950 | hp1 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18951 | hp1 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0333 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18952 | hp2 | a0002 | c0004 | t0001 | g0037 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18960 | hp1 | a0004 | c0006 | t0001 | g0008 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18962 | hp2 | a0002 | c0004 | t0001 | g0037 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18963 | hp1 | a0003 | c0005 | t0001 | g0296 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18963 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18964 | hp1 | a0001 | c0033 | t0001 | g0261 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18964 | hp2 | a0011 | c0026 | t0001 | g0145 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18965 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18967 | hp2 | a0002 | c0004 | t0001 | g0247 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18974 | hp2 | a0004 | c0006 | t0001 | g0008 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18977 | hp1 | a0003 | c0005 | t0001 | g0275 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18981 | hp1 | a0002 | c0004 | t0001 | g0246 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18981 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18984 | hp2 | a0002 | c0004 | t0001 | g0283 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18985 | hp1 | a0003 | c0005 | t0002 | g0297 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18987 | hp2 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18988 | hp2 | a0002 | c0004 | t0001 | g0038 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18990 | hp2 | a0003 | c0005 | t0001 | g0010 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18995 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18995 | hp2 | a0002 | c0004 | t0001 | g0012 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19001 | hp2 | a0003 | c0005 | t0001 | g0010 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19002 | hp1 | a0002 | c0004 | t0001 | g0012 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0331 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19003 | hp2 | a0004 | c0006 | t0001 | g0258 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19004 | hp1 | a0003 | c0005 | t0001 | g0010 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19005 | hp1 | a0003 | c0005 | t0001 | g0269 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19007 | hp1 | a0002 | c0004 | t0001 | g0242 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19009 | hp1 | a0003 | c0005 | t0001 | g0294 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19010 | hp2 | a0003 | c0005 | t0001 | g0278 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19011 | hp1 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | LWK | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19030 | hp2 | a0006 | c0008 | t0001 | g0339 | AFR | LWK | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | LWK | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19043 | hp2 | a0009 | c0011 | t0001 | g0041 | AFR | LWK | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19055 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19056 | hp2 | a0004 | c0006 | t0001 | g0008 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19057 | hp1 | a0002 | c0004 | t0001 | g0284 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19058 | hp1 | a0003 | c0005 | t0001 | g0272 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19060 | hp1 | a0003 | c0005 | t0001 | g0324 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19068 | hp1 | a0004 | c0006 | t0001 | g0256 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19070 | hp1 | a0004 | c0006 | t0001 | g0289 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19075 | hp1 | a0028 | c0035 | t0001 | g0155 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19076 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19076 | hp2 | a0003 | c0005 | t0001 | g0317 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19078 | hp1 | a0003 | c0005 | t0001 | g0010 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19078 | hp2 | a0001 | c0002 | t0003 | g0088 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19081 | hp2 | a0004 | c0006 | t0001 | g0245 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0027 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19083 | hp1 | a0001 | c0003 | t0001 | g0334 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19083 | hp2 | a0017 | c0017 | t0001 | g0270 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19085 | hp2 | a0004 | c0006 | t0001 | g0251 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19088 | hp2 | a0004 | c0006 | t0001 | g0008 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19089 | hp1 | a0004 | c0006 | t0001 | g0040 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19091 | hp2 | a0017 | c0017 | t0001 | g0111 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19240 | hp1 | a0010 | c0013 | t0004 | g0129 | AFR | YRI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | YRI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ASW | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20129 | hp2 | a0010 | c0030 | t0004 | g0263 | AFR | ASW | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20752 | hp2 | a0002 | c0004 | t0001 | g0182 | EUR | TSI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20805 | hp1 | a0002 | c0004 | t0001 | g0001 | EUR | TSI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0019 | EUR | TSI | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0076 | SAS | GIH | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01123 | hp1 | a0002 | c0004 | t0001 | g0237 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02109 | hp1 | a0013 | c0015 | t0003 | g0121 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02486 | hp1 | a0006 | c0021 | t0001 | g0117 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG03471 | hp2 | a0010 | c0013 | t0004 | g0126 | AFR | MSL | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | USA | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | USA | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18955 | hp1 | a0002 | c0004 | t0001 | g0248 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | USA | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | USA | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA21309 | hp1 | a0029 | c0044 | t0001 | g0344 | AFR | LWK | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
NA21309 | hp2 | a0002 | c0004 | t0001 | g0001 | AFR | LWK | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
homoSapiens | chm13v2 | a0002 | c0004 | t0001 | g0212 | REF | REF | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
homoSapiens | grch38p0 | a0003 | c0005 | t0001 | g0013 | REF | REF | CD101_chr1_116996760_117041552 | CD101 | chr1 | 116996760 | 117041552 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117010105 | A | G | 1 | a0029 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.299A>G | p.Gln100Arg | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/10 | 357/3542 | 299/3066 | 100/1021 | chr1 | 117010105 | |||
chr1:117010183 | C | A | 1 | a0020 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.377C>A | p.Thr126Asn | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/10 | 435/3542 | 377/3066 | 126/1021 | chr1 | 117010183 | |||
chr1:117011594 | G | A | 2 | a0009 a0025 |
5 | HG02630.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.469G>A | p.Gly157Ser | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/10 | 527/3542 | 469/3066 | 157/1021 | chr1 | 117011594 | |||
chr1:117011789 | G | A | 1 | a0011 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.664G>A | p.Val222Ile | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/10 | 722/3542 | 664/3066 | 222/1021 | chr1 | 117011789 | |||
chr1:117011789 | G | C | 1 | a0011 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.664G>C | p.Val222Leu | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/10 | 722/3542 | 664/3066 | 222/1021 | chr1 | 117011789 | |||
chr1:117011799 | A | G | 4 | a0002 a0022 a0023 others(1): Show |
54 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
missense_variant | MODERATE | c.674A>G | p.Asn225Ser | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/10 | 732/3542 | 674/3066 | 225/1021 | chr1 | 117011799 | |||
chr1:117011880 | C | T | 1 | a0018 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.755C>T | p.Thr252Met | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/10 | 813/3542 | 755/3066 | 252/1021 | chr1 | 117011880 | |||
chr1:117017104 | A | G | 26 | a0001 a0002 a0004 others(23): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
missense_variant | MODERATE | c.1243A>G | p.Met415Val | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/10 | 1301/3542 | 1243/3066 | 415/1021 | chr1 | 117017104 | |||
chr1:117017216 | G | A | 1 | a0017 | 2 | NA19083.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.1355G>A | p.Arg452Gln | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/10 | 1413/3542 | 1355/3066 | 452/1021 | chr1 | 117017216 | |||
chr1:117017429 | A | G | 1 | a0019 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1568A>G | p.Asp523Gly | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/10 | 1626/3542 | 1568/3066 | 523/1021 | chr1 | 117017429 | |||
chr1:117017436 | C | G | 3 | a0005 a0012 a0013 |
14 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(11): Show |
missense_variant | MODERATE | c.1575C>G | p.Ser525Arg | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/10 | 1633/3542 | 1575/3066 | 525/1021 | chr1 | 117017436 | |||
chr1:117018368 | C | T | 1 | a0025 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1825C>T | p.Arg609Trp | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 1883/3542 | 1825/3066 | 609/1021 | chr1 | 117018368 | |||
chr1:117018408 | G | A | 1 | a0024 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1865G>A | p.Arg622His | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 1923/3542 | 1865/3066 | 622/1021 | chr1 | 117018408 | |||
chr1:117018494 | T | G | 2 | a0015 a0024 |
3 | HG02622.hp2 HG02818.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1951T>G | p.Tyr651Asp | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 2009/3542 | 1951/3066 | 651/1021 | chr1 | 117018494 | |||
chr1:117021794 | A | G | 1 | a0020 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.2239A>G | p.Arg747Gly | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/10 | 2297/3542 | 2239/3066 | 747/1021 | chr1 | 117021794 | |||
chr1:117025578 | G | A | 2 | a0004 a0018 |
15 | HG00408.hp2 HG02056.hp1 HG02083.hp1 others(12): Show |
missense_variant | MODERATE | c.2498G>A | p.Arg833His | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/10 | 2556/3542 | 2498/3066 | 833/1021 | chr1 | 117025578 | |||
chr1:117025595 | G | A | 1 | a0008 | 5 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
missense_variant | MODERATE | c.2515G>A | p.Val839Ile | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/10 | 2573/3542 | 2515/3066 | 839/1021 | chr1 | 117025595 | |||
chr1:117025811 | G | A | 1 | a0021 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2731G>A | p.Val911Met | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/10 | 2789/3542 | 2731/3066 | 911/1021 | chr1 | 117025811 | |||
chr1:117025878 | G | A | 3 | a0006 a0022 a0029 |
9 | HG01891.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
missense_variant | MODERATE | c.2798G>A | p.Arg933Gln | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/10 | 2856/3542 | 2798/3066 | 933/1021 | chr1 | 117025878 | |||
chr1:117025892 | G | A | 1 | a0028 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.2812G>A | p.Val938Met | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/10 | 2870/3542 | 2812/3066 | 938/1021 | chr1 | 117025892 | |||
chr1:117033900 | A | T | 3 | a0007 a0016 a0027 |
9 | HG01168.hp1 HG01169.hp2 HG01516.hp1 others(6): Show |
missense_variant | MODERATE | c.2865A>T | p.Leu955Phe | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 2923/3542 | 2865/3066 | 955/1021 | chr1 | 117033900 | |||
chr1:117033922 | C | G | 1 | a0026 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2887C>G | p.Pro963Ala | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 2945/3542 | 2887/3066 | 963/1021 | chr1 | 117033922 | |||
chr1:117033928 | G | A | 2 | a0013 a0022 |
3 | HG02109.hp1 HG02647.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.2893G>A | p.Val965Ile | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 2951/3542 | 2893/3066 | 965/1021 | chr1 | 117033928 | |||
chr1:117033967 | T | C | 1 | a0012 | 2 | HG01433.hp2 HG02717.hp2 |
missense_variant | MODERATE | c.2932T>C | p.Tyr978His | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 2990/3542 | 2932/3066 | 978/1021 | chr1 | 117033967 | |||
chr1:117033997 | C | T | 1 | a0022 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.2962C>T | p.Arg988Cys | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 3020/3542 | 2962/3066 | 988/1021 | chr1 | 117033997 | |||
chr1:117034009 | C | T | 1 | a0010 | 3 | HG03471.hp2 NA19240.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.2974C>T | p.Arg992Trp | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 3032/3542 | 2974/3066 | 992/1021 | chr1 | 117034009 | |||
chr1:117034057 | A | G | 1 | a0014 | 2 | HG02280.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.3022A>G | p.Thr1008Ala | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 3080/3542 | 3022/3066 | 1008/1021 | chr1 | 117034057 | |||
chr1:117034068 | GAGGGAAG others(26): Show |
G | 1 | a0023 | 1 | HG02683.hp2 | stop_lost&conservative_inframe_deletion | HIGH | c.3035_*1delGGGAAGAC others(25): Show |
p.Arg1012_Ter1022del others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 3093/3542 | 3035/3066 | 1012/1021 | INFO_REALIGN_3_PRIME | chr1 | 117034068 | ||
chr1:117036170 | T | G | 1 | a0001 | 1 | HG02055.hp2 | splice_region_variant | LOW | c.*36T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 10/10 | chr1 | 117036170 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117009938 | T | C | 7 | a0001c0010 a0001c0022 a0005c0007 others(4): Show |
22 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(19): Show |
synonymous_variant | LOW | c.132T>C | p.Asn44Asn | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/10 | 190/3542 | 132/3066 | 44/1021 | chr1 | 117009938 | |||
chr1:117013503 | A | G | 1 | a0013c0015 | 2 | HG02109.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.939A>G | p.Pro313Pro | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/10 | 997/3542 | 939/3066 | 313/1021 | chr1 | 117013503 | |||
chr1:117013683 | C | T | 1 | a0001c0038 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.1119C>T | p.Gly373Gly | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/10 | 1177/3542 | 1119/3066 | 373/1021 | chr1 | 117013683 | |||
chr1:117013731 | C | T | 2 | a0006c0021 a0029c0044 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.1167C>T | p.Ser389Ser | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/10 | 1225/3542 | 1167/3066 | 389/1021 | chr1 | 117013731 | |||
chr1:117017160 | C | T | 1 | a0012c0014 | 2 | HG01433.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.1299C>T | p.Leu433Leu | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/10 | 1357/3542 | 1299/3066 | 433/1021 | chr1 | 117017160 | |||
chr1:117018196 | A | G | 11 | a0001c0002 a0001c0003 a0001c0034 others(8): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
synonymous_variant | LOW | c.1653A>G | p.Gln551Gln | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 1711/3542 | 1653/3066 | 551/1021 | chr1 | 117018196 | |||
chr1:117018214 | C | A | 1 | a0001c0022 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1671C>A | p.Thr557Thr | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 1729/3542 | 1671/3066 | 557/1021 | chr1 | 117018214 | |||
chr1:117018241 | C | T | 1 | a0022c0043 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1698C>T | p.Ala566Ala | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 1756/3542 | 1698/3066 | 566/1021 | chr1 | 117018241 | |||
chr1:117018307 | C | A | 6 | a0001c0002 a0001c0038 a0007c0020 others(3): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
synonymous_variant | LOW | c.1764C>A | p.Ile588Ile | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/10 | 1822/3542 | 1764/3066 | 588/1021 | chr1 | 117018307 | |||
chr1:117021586 | A | G | 1 | a0001c0033 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.2031A>G | p.Lys677Lys | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/10 | 2089/3542 | 2031/3066 | 677/1021 | chr1 | 117021586 | |||
chr1:117021703 | T | C | 1 | a0001c0034 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2148T>C | p.Ser716Ser | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/10 | 2206/3542 | 2148/3066 | 716/1021 | chr1 | 117021703 | |||
chr1:117025726 | G | A | 1 | a0002c0040 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.2646G>A | p.Leu882Leu | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/10 | 2704/3542 | 2646/3066 | 882/1021 | chr1 | 117025726 | |||
chr1:117033990 | A | G | 1 | a0001c0031 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2955A>G | p.Ser985Ser | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/10 | 3013/3542 | 2955/3066 | 985/1021 | chr1 | 117033990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117036202 | C | T | 1 | a0001c0002t0007 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 10/10 | 2101 | chr1 | 117036202 | ||||||
chr1:117036486 | T | C | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(5): Show |
31 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*352T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 10/10 | 2385 | chr1 | 117036486 | ||||||
chr1:117036517 | T | TA | 11 | a0001c0001t0003 a0001c0002t0003 a0001c0010t0003 others(8): Show |
22 | HG00280.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*398dupA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 10/10 | 2432 | INFO_REALIGN_3_PRIME | chr1 | 117036517 | |||||
chr1:117036517 | TA | T | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(10): Show |
41 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*398delA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 10/10 | 2431 | INFO_REALIGN_3_PRIME | chr1 | 117036517 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117002050 | A | G | 3 | a0012c0014t0001g0342 a0012c0014t0001g0343 a0029c0044t0001g0344 |
3 | HG01433.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.43+190A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002050 | |||||||
chr1:117002080 | T | C | 76 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0017 others(73): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.43+220T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002080 | |||||||
chr1:117002153 | C | T | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+293C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002153 | |||||||
chr1:117002257 | T | C | 20 | a0001c0001t0001g0120 a0001c0001t0003g0119 a0001c0001t0004g0118 others(17): Show |
20 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.43+397T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002257 | |||||||
chr1:117002393 | A | T | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+533A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002393 | |||||||
chr1:117002523 | A | G | 6 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0336 others(3): Show |
6 | HG00673.hp1 HG02056.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+663A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002523 | |||||||
chr1:117002599 | T | C | 1 | a0001c0002t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.43+739T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117002599 | |||||||
chr1:117003072 | G | A | 1 | a0002c0004t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.43+1212G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003072 | |||||||
chr1:117003205 | C | T | 3 | a0015c0019t0001g0135 a0015c0019t0002g0134 a0024c0027t0001g0133 |
3 | HG02622.hp2 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+1345C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003205 | |||||||
chr1:117003207 | G | A | 3 | a0015c0019t0001g0135 a0015c0019t0002g0134 a0024c0027t0001g0133 |
3 | HG02622.hp2 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+1347G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003207 | |||||||
chr1:117003310 | G | C | 76 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0017 others(73): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.43+1450G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003310 | |||||||
chr1:117003356 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+1496G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003356 | |||||||
chr1:117003399 | G | T | 2 | a0001c0003t0001g0131 a0001c0003t0001g0132 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.43+1539G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003399 | |||||||
chr1:117003433 | C | T | 1 | a0020c0024t0003g0332 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.43+1573C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003433 | |||||||
chr1:117003462 | G | A | 3 | a0015c0019t0001g0135 a0015c0019t0002g0134 a0024c0027t0001g0133 |
3 | HG02622.hp2 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+1602G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003462 | |||||||
chr1:117003619 | A | G | 1 | a0001c0003t0001g0331 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.43+1759A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003619 | |||||||
chr1:117003756 | C | G | 8 | a0001c0010t0003g0123 a0001c0010t0003g0124 a0001c0010t0003g0125 others(5): Show |
8 | HG02280.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+1896C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003756 | |||||||
chr1:117003932 | C | T | 5 | a0013c0015t0001g0122 a0013c0015t0003g0121 a0015c0019t0001g0135 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+2072C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003932 | |||||||
chr1:117003942 | A | T | 8 | a0003c0005t0001g0325 a0005c0007t0001g0014 a0005c0007t0001g0052 others(5): Show |
11 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+2082A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003942 | |||||||
chr1:117003965 | T | G | 6 | a0013c0015t0001g0122 a0013c0015t0003g0121 a0015c0019t0001g0135 others(3): Show |
6 | HG02109.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+2105T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003965 | |||||||
chr1:117003974 | G | C | 1 | a0002c0004t0001g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.43+2114G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003974 | |||||||
chr1:117003989 | T | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(217): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.43+2129T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117003989 | |||||||
chr1:117004066 | G | A | 1 | a0001c0003t0001g0139 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.43+2206G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004066 | |||||||
chr1:117004069 | T | C | 5 | a0013c0015t0001g0122 a0013c0015t0003g0121 a0015c0019t0001g0135 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+2209T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004069 | |||||||
chr1:117004147 | G | A | 1 | a0001c0002t0001g0055 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.43+2287G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004147 | |||||||
chr1:117004147 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.43+2287G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004147 | |||||||
chr1:117004507 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0003g0119 a0001c0001t0004g0118 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+2647A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004507 | |||||||
chr1:117004637 | T | G | 3 | a0015c0019t0001g0135 a0015c0019t0002g0134 a0024c0027t0001g0133 |
3 | HG02622.hp2 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+2777T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004637 | |||||||
chr1:117004642 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.43+2782C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004642 | |||||||
chr1:117004658 | T | C | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+2798T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004658 | |||||||
chr1:117004751 | C | G | 1 | a0003c0005t0001g0324 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.43+2891C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004751 | |||||||
chr1:117004753 | T | C | 134 | a0001c0001t0001g0140 a0001c0001t0001g0179 a0001c0001t0001g0180 others(131): Show |
161 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.43+2893T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004753 | |||||||
chr1:117004761 | A | G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0221 a0001c0001t0003g0220 others(8): Show |
13 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+2901A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004761 | |||||||
chr1:117004763 | C | G | 138 | a0001c0001t0001g0140 a0001c0001t0001g0179 a0001c0001t0001g0180 others(135): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.43+2903C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004763 | |||||||
chr1:117004839 | G | A | 1 | a0002c0004t0001g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.43+2979G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004839 | |||||||
chr1:117004873 | T | G | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+3013T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004873 | |||||||
chr1:117004875 | G | A | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+3015G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117004875 | |||||||
chr1:117005048 | A | G | 1 | a0001c0002t0001g0113 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.43+3188A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005048 | |||||||
chr1:117005168 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(33): Show |
45 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.43+3308G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005168 | |||||||
chr1:117005195 | C | A | 2 | a0001c0003t0001g0033 a0001c0003t0001g0217 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.43+3335C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005195 | |||||||
chr1:117005258 | A | T | 138 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0002t0001g0003 others(135): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.43+3398A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005258 | |||||||
chr1:117005270 | C | G | 1 | a0001c0002t0002g0112 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.43+3410C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005270 | |||||||
chr1:117005271 | G | A | 1 | a0001c0003t0001g0025 | 2 | NA18990.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.43+3411G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005271 | |||||||
chr1:117005320 | C | G | 1 | a0001c0003t0001g0181 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.43+3460C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005320 | |||||||
chr1:117005347 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(37): Show |
49 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.43+3487G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005347 | |||||||
chr1:117005394 | C | T | 1 | a0002c0004t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.43+3534C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005394 | |||||||
chr1:117005479 | A | G | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.43+3619A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005479 | |||||||
chr1:117005700 | C | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(39): Show |
51 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.43+3840C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005700 | |||||||
chr1:117005895 | C | T | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-3955C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005895 | |||||||
chr1:117005905 | C | G | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG00099.hp1 HG01175.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.44-3945C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005905 | |||||||
chr1:117005978 | A | T | 1 | a0001c0002t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.44-3872A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117005978 | |||||||
chr1:117006036 | T | C | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.44-3814T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006036 | |||||||
chr1:117006100 | A | G | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-3750A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006100 | |||||||
chr1:117006118 | C | A | 1 | a0003c0005t0002g0035 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.44-3732C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006118 | |||||||
chr1:117006159 | G | C | 1 | a0001c0002t0001g0056 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.44-3691G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006159 | |||||||
chr1:117006173 | TC | T | 2 | a0001c0001t0001g0320 a0007c0012t0001g0051 |
3 | HG01168.hp1 HG01169.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.44-3675delC | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 117006173 | ||||||
chr1:117006633 | T | C | 1 | a0026c0032t0002g0228 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.44-3217T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006633 | |||||||
chr1:117006684 | C | T | 1 | a0006c0008t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44-3166C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006684 | |||||||
chr1:117006687 | A | G | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.44-3163A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006687 | |||||||
chr1:117006691 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.44-3159C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006691 | |||||||
chr1:117006763 | A | G | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.44-3087A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006763 | |||||||
chr1:117006883 | G | A | 136 | a0001c0001t0001g0179 a0001c0002t0001g0003 a0001c0002t0001g0015 others(133): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.44-2967G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117006883 | |||||||
chr1:117007000 | C | T | 2 | a0002c0004t0001g0318 a0002c0004t0001g0319 |
2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.44-2850C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007000 | |||||||
chr1:117007046 | A | G | 4 | a0005c0007t0001g0014 a0005c0007t0001g0328 a0005c0007t0001g0329 others(1): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-2804A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007046 | |||||||
chr1:117007248 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.44-2602A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007248 | |||||||
chr1:117007252 | C | T | 1 | a0003c0005t0001g0317 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.44-2598C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007252 | |||||||
chr1:117007253 | G | A | 1 | a0001c0002t0001g0057 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.44-2597G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007253 | |||||||
chr1:117007288 | G | T | 1 | a0003c0005t0002g0316 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.44-2562G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007288 | |||||||
chr1:117007330 | C | T | 2 | a0001c0001t0001g0179 a0001c0003t0004g0178 |
2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.44-2520C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007330 | |||||||
chr1:117007390 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0003g0215 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.44-2460C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007390 | |||||||
chr1:117007391 | G | T | 1 | a0001c0002t0001g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.44-2459G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007391 | |||||||
chr1:117007434 | G | A | 139 | a0001c0001t0001g0179 a0001c0002t0001g0003 a0001c0002t0001g0015 others(136): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.44-2416G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007434 | |||||||
chr1:117007446 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
8 | HG02109.hp2 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-2404C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007446 | |||||||
chr1:117007480 | T | A | 8 | a0001c0010t0003g0123 a0001c0010t0003g0124 a0001c0010t0003g0125 others(5): Show |
8 | HG02280.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-2370T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007480 | |||||||
chr1:117007504 | A | G | 2 | a0003c0005t0001g0311 a0003c0005t0002g0316 |
2 | HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.44-2346A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007504 | |||||||
chr1:117007577 | C | G | 136 | a0001c0001t0001g0179 a0001c0002t0001g0003 a0001c0002t0001g0015 others(133): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.44-2273C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007577 | |||||||
chr1:117007612 | A | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(218): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.44-2238A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007612 | |||||||
chr1:117007640 | G | T | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-2210G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007640 | |||||||
chr1:117007685 | G | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
5 | HG02258.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-2165G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007685 | |||||||
chr1:117007694 | A | G | 3 | a0006c0021t0001g0116 a0006c0021t0001g0117 a0029c0044t0001g0344 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.44-2156A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007694 | |||||||
chr1:117007705 | C | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(34): Show |
46 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.44-2145C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007705 | |||||||
chr1:117007813 | T | A | 1 | a0001c0003t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.44-2037T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007813 | |||||||
chr1:117007846 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.44-2004G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007846 | |||||||
chr1:117007862 | C | T | 1 | a0014c0023t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-1988C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007862 | |||||||
chr1:117007870 | T | C | 1 | a0002c0004t0001g0231 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.44-1980T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007870 | |||||||
chr1:117007893 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.44-1957C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117007893 | |||||||
chr1:117008000 | G | A | 5 | a0001c0002t0001g0058 a0001c0002t0002g0059 a0001c0002t0002g0060 others(2): Show |
5 | HG02523.hp1 NA18612.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-1850G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008000 | |||||||
chr1:117008001 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(218): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.44-1849A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008001 | |||||||
chr1:117008011 | A | T | 3 | a0001c0002t0001g0054 a0001c0002t0001g0109 a0019c0037t0001g0108 |
3 | HG00621.hp2 HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.44-1839A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008011 | |||||||
chr1:117008141 | T | C | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.44-1709T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008141 | |||||||
chr1:117008325 | C | T | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.44-1525C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008325 | |||||||
chr1:117008406 | A | G | 1 | a0001c0002t0001g0107 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44-1444A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008406 | |||||||
chr1:117008462 | CA | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0205 a0001c0002t0001g0056 others(3): Show |
7 | HG00735.hp2 HG01934.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-1375delA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 117008462 | ||||||
chr1:117008481 | A | C | 8 | a0003c0005t0001g0325 a0005c0007t0001g0014 a0005c0007t0001g0052 others(5): Show |
11 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.44-1369A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008481 | |||||||
chr1:117008490 | G | T | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-1360G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008490 | |||||||
chr1:117008535 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0003g0222 |
2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.44-1315A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008535 | |||||||
chr1:117008625 | A | G | 1 | a0002c0040t0001g0310 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.44-1225A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008625 | |||||||
chr1:117008693 | C | T | 10 | a0001c0002t0001g0024 a0001c0002t0001g0097 a0001c0002t0001g0098 others(7): Show |
11 | HG00738.hp1 HG01106.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-1157C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008693 | |||||||
chr1:117008734 | A | T | 4 | a0002c0004t0002g0308 a0002c0004t0002g0309 a0002c0004t0003g0048 others(1): Show |
5 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1116A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008734 | |||||||
chr1:117008739 | G | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG00735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.44-1111G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008739 | |||||||
chr1:117008807 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0002g0049 a0001c0001t0002g0312 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-1043G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008807 | |||||||
chr1:117008878 | A | G | 1 | a0001c0003t0001g0176 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.44-972A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008878 | |||||||
chr1:117008879 | C | T | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-971C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117008879 | |||||||
chr1:117009018 | T | G | 2 | a0002c0004t0001g0234 a0002c0004t0001g0235 |
2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.44-832T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009018 | |||||||
chr1:117009083 | C | T | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.44-767C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009083 | |||||||
chr1:117009245 | C | G | 8 | a0001c0010t0003g0123 a0001c0010t0003g0124 a0001c0010t0003g0125 others(5): Show |
8 | HG02280.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-605C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009245 | |||||||
chr1:117009311 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.44-539G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009311 | |||||||
chr1:117009362 | G | A | 172 | a0001c0001t0001g0034 a0001c0001t0001g0179 a0001c0001t0001g0214 others(169): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.44-488G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009362 | |||||||
chr1:117009457 | T | C | 61 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0006 others(58): Show |
79 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.44-393T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009457 | |||||||
chr1:117009590 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.44-260C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009590 | |||||||
chr1:117009600 | T | A | 1 | a0016c0018t0001g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.44-250T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009600 | |||||||
chr1:117009604 | G | T | 7 | a0005c0007t0001g0014 a0005c0007t0001g0052 a0005c0007t0001g0327 others(4): Show |
10 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-246G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009604 | |||||||
chr1:117009699 | T | G | 8 | a0001c0010t0003g0123 a0001c0010t0003g0124 a0001c0010t0003g0125 others(5): Show |
8 | HG02280.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-151T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009699 | |||||||
chr1:117009787 | T | G | 17 | a0001c0002t0001g0024 a0001c0002t0001g0058 a0001c0002t0001g0097 others(14): Show |
18 | HG00544.hp1 HG00738.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-63T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 1/9 | chr1 | 117009787 | |||||||
chr1:117010506 | A | G | 2 | a0001c0003t0001g0337 a0001c0003t0001g0338 |
2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.424+276A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117010506 | |||||||
chr1:117010515 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.424+285A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117010515 | |||||||
chr1:117010577 | G | C | 1 | a0003c0005t0002g0316 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.424+347G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117010577 | |||||||
chr1:117010601 | G | T | 2 | a0009c0011t0001g0304 a0009c0011t0001g0305 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.424+371G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117010601 | |||||||
chr1:117010780 | C | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.424+550C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117010780 | |||||||
chr1:117011017 | C | A | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-533C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011017 | |||||||
chr1:117011115 | A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.425-435A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011115 | |||||||
chr1:117011183 | T | C | 3 | a0006c0021t0001g0116 a0006c0021t0001g0117 a0029c0044t0001g0344 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.425-367T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011183 | |||||||
chr1:117011322 | G | A | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-228G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011322 | |||||||
chr1:117011339 | G | T | 2 | a0006c0021t0001g0116 a0006c0021t0001g0117 |
2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.425-211G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011339 | |||||||
chr1:117011424 | A | G | 1 | a0001c0002t0002g0095 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.425-126A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011424 | |||||||
chr1:117011457 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0003g0119 a0001c0001t0004g0118 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.425-93G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011457 | |||||||
chr1:117011482 | C | T | 3 | a0002c0004t0001g0046 a0002c0004t0001g0047 a0002c0004t0001g0303 |
5 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.425-68C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 2/9 | chr1 | 117011482 | |||||||
chr1:117011982 | C | T | 1 | a0001c0003t0002g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.841+16C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117011982 | |||||||
chr1:117012100 | T | C | 1 | a0002c0004t0001g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.841+134T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012100 | |||||||
chr1:117012195 | A | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.841+229A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012195 | |||||||
chr1:117012283 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.841+317C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012283 | |||||||
chr1:117012303 | G | T | 1 | a0010c0013t0004g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.841+337G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012303 | |||||||
chr1:117012390 | A | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(38): Show |
50 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.841+424A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012390 | |||||||
chr1:117012698 | G | T | 1 | a0001c0001t0001g0300 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.842-708G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012698 | |||||||
chr1:117012706 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.842-700C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012706 | |||||||
chr1:117012848 | A | G | 2 | a0001c0001t0004g0218 a0001c0001t0004g0219 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.842-558A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012848 | |||||||
chr1:117012852 | T | C | 20 | a0001c0010t0003g0123 a0001c0010t0003g0124 a0001c0010t0003g0125 others(17): Show |
23 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.842-554T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012852 | |||||||
chr1:117012882 | T | C | 5 | a0001c0002t0001g0058 a0001c0002t0002g0059 a0001c0002t0002g0060 others(2): Show |
5 | HG02523.hp1 NA18612.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.842-524T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012882 | |||||||
chr1:117012907 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0003g0203 |
2 | HG00280.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.842-499C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117012907 | |||||||
chr1:117013005 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0030 |
7 | NA18953.hp2 NA18974.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-401G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117013005 | |||||||
chr1:117013157 | A | G | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.842-249A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117013157 | |||||||
chr1:117013255 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.842-151T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117013255 | |||||||
chr1:117013263 | G | C | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.842-143G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117013263 | |||||||
chr1:117013276 | G | A | 345 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(342): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.842-130G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 3/9 | chr1 | 117013276 | |||||||
chr1:117013804 | C | G | 4 | a0002c0004t0002g0308 a0002c0004t0002g0309 a0002c0004t0003g0048 others(1): Show |
5 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228+12C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117013804 | |||||||
chr1:117013864 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0003g0203 |
2 | HG00280.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1228+72G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117013864 | |||||||
chr1:117013873 | A | G | 1 | a0001c0003t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1228+81A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117013873 | |||||||
chr1:117014054 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1228+262G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014054 | |||||||
chr1:117014177 | C | T | 15 | a0001c0002t0001g0109 a0001c0003t0001g0007 a0001c0003t0001g0028 others(12): Show |
20 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228+385C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014177 | |||||||
chr1:117014185 | T | TTG | 45 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(42): Show |
52 | HG00280.hp1 HG00597.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1228+436_1228+437d others(4): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | T | TTGTG | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0137 others(38): Show |
53 | HG00597.hp2 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1228+434_1228+437d others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | T | TTGTGTG | 24 | a0001c0001t0001g0186 a0001c0001t0001g0214 a0001c0001t0003g0215 others(21): Show |
29 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1228+432_1228+437d others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | T | TTGTGTGT others(1): Show |
5 | a0001c0003t0001g0004 a0001c0003t0001g0006 a0001c0003t0001g0033 others(2): Show |
6 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+430_1228+437d others(10): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTG | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0034 others(5): Show |
8 | HG00558.hp1 HG01433.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1228+436_1228+437d others(4): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTG | T | 71 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0041 others(68): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228+434_1228+437d others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTGTG | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0259 a0001c0001t0001g0285 others(3): Show |
7 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1228+432_1228+437d others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTGTGT others(1): Show |
T | 51 | a0001c0001t0001g0036 a0001c0001t0001g0253 a0001c0001t0001g0300 others(48): Show |
67 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1228+430_1228+437d others(10): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTGTGT others(3): Show |
T | 1 | a0002c0040t0001g0310 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1228+428_1228+437d others(12): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTGTGT others(5): Show |
T | 4 | a0001c0001t0004g0213 a0006c0021t0001g0116 a0006c0021t0001g0117 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228+426_1228+437d others(14): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTGTGT others(7): Show |
T | 3 | a0001c0001t0001g0120 a0001c0001t0003g0119 a0001c0001t0004g0118 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1228+424_1228+437d others(16): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014185 | TTGTGTGT others(17): Show |
T | 1 | a0001c0003t0001g0028 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228+414_1228+437d others(26): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014185 | ||||||
chr1:117014228 | T | TGA | 5 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228+437_1228+438d others(4): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014228 | ||||||
chr1:117014228 | T | TGTGA | 5 | a0001c0002t0001g0015 a0001c0002t0001g0070 a0001c0002t0001g0071 others(2): Show |
6 | HG02027.hp1 HG02155.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228+437_1228+438i others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014228 | ||||||
chr1:117014228 | T | TGTGTGA | 50 | a0001c0002t0001g0003 a0001c0002t0001g0017 a0001c0002t0001g0018 others(47): Show |
58 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1228+437_1228+438i others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014228 | ||||||
chr1:117014228 | T | TGTGTGTG others(1): Show |
8 | a0001c0002t0001g0023 a0001c0002t0001g0058 a0001c0002t0001g0089 others(5): Show |
9 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228+437_1228+438i others(10): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014228 | ||||||
chr1:117014228 | T | TGTGTGTG others(3): Show |
6 | a0001c0002t0001g0093 a0001c0002t0002g0060 a0001c0002t0002g0061 others(3): Show |
6 | HG02165.hp1 HG02523.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+437_1228+438i others(12): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014228 | ||||||
chr1:117014228 | T | TGTGTGTG others(5): Show |
1 | a0001c0002t0001g0094 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1228+437_1228+438i others(14): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117014228 | ||||||
chr1:117014258 | C | T | 1 | a0001c0002t0002g0061 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1228+466C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014258 | |||||||
chr1:117014462 | T | C | 1 | a0001c0003t0001g0142 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1228+670T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014462 | |||||||
chr1:117014474 | G | A | 1 | a0007c0036t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1228+682G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014474 | |||||||
chr1:117014609 | G | A | 170 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0003g0215 others(167): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1228+817G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014609 | |||||||
chr1:117014671 | C | A | 1 | a0001c0002t0003g0088 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1228+879C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014671 | |||||||
chr1:117014747 | A | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01123.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1228+955A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014747 | |||||||
chr1:117014825 | C | T | 8 | a0003c0005t0001g0010 a0003c0005t0001g0294 a0003c0005t0001g0295 others(5): Show |
11 | HG02071.hp1 HG02129.hp1 NA18963.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228+1033C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014825 | |||||||
chr1:117014840 | T | A | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1228+1048T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014840 | |||||||
chr1:117014963 | T | C | 8 | a0003c0005t0001g0325 a0005c0007t0001g0014 a0005c0007t0001g0052 others(5): Show |
11 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228+1171T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014963 | |||||||
chr1:117014984 | A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1228+1192A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117014984 | |||||||
chr1:117015010 | G | A | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228+1218G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117015010 | |||||||
chr1:117015110 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1228+1318G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117015110 | |||||||
chr1:117015135 | T | C | 2 | a0001c0003t0001g0026 a0001c0003t0001g0141 |
3 | NA18941.hp1 NA18943.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1228+1343T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117015135 | |||||||
chr1:117015356 | A | T | 1 | a0006c0008t0001g0053 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1228+1564A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117015356 | |||||||
chr1:117015407 | G | GAGATTAT others(7): Show |
173 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0001g0221 others(170): Show |
206 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1228+1616_1228+161 others(18): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117015407 | ||||||
chr1:117015446 | AT | A | 3 | a0006c0021t0001g0116 a0006c0021t0001g0117 a0029c0044t0001g0344 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-1639delT | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117015446 | ||||||
chr1:117015738 | T | G | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1229-1352T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117015738 | |||||||
chr1:117016100 | C | T | 7 | a0005c0007t0001g0014 a0005c0007t0001g0052 a0005c0007t0001g0327 others(4): Show |
10 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1229-990C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016100 | |||||||
chr1:117016186 | TTA | T | 5 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(2): Show |
6 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-890_1229-889d others(4): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 117016186 | ||||||
chr1:117016202 | T | A | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1229-888T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016202 | |||||||
chr1:117016243 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1229-847G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016243 | |||||||
chr1:117016672 | A | G | 1 | a0013c0015t0001g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1229-418A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016672 | |||||||
chr1:117016686 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0205 |
3 | HG00735.hp2 HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1229-404G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016686 | |||||||
chr1:117016871 | T | G | 3 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0089 |
3 | HG02738.hp2 HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1229-219T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016871 | |||||||
chr1:117016882 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0004g0218 a0001c0001t0004g0219 others(1): Show |
5 | HG02559.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1229-208G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016882 | |||||||
chr1:117016976 | C | A | 56 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0006 others(53): Show |
73 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1229-114C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117016976 | |||||||
chr1:117017039 | T | C | 2 | a0003c0005t0001g0010 a0003c0005t0001g0294 |
5 | NA18990.hp2 NA19001.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1229-51T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 4/9 | chr1 | 117017039 | |||||||
chr1:117017503 | C | T | 1 | a0012c0014t0001g0343 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1612+30C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017503 | |||||||
chr1:117017543 | G | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0001g0221 others(8): Show |
12 | HG02145.hp2 HG02622.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1612+70G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017543 | |||||||
chr1:117017544 | C | T | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1612+71C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017544 | |||||||
chr1:117017754 | G | T | 1 | a0001c0003t0001g0007 | 4 | NA18942.hp1 NA19055.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1612+281G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017754 | |||||||
chr1:117017778 | A | T | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1612+305A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017778 | |||||||
chr1:117017828 | C | G | 1 | a0002c0004t0001g0291 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1613-328C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017828 | |||||||
chr1:117017920 | A | G | 137 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0017 others(134): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1613-236A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117017920 | |||||||
chr1:117018033 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0003g0119 a0001c0001t0004g0118 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1613-123T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117018033 | |||||||
chr1:117018035 | G | T | 3 | a0006c0021t0001g0116 a0006c0021t0001g0117 a0029c0044t0001g0344 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1613-121G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117018035 | |||||||
chr1:117018133 | T | G | 2 | a0001c0002t0002g0062 a0001c0002t0002g0063 |
2 | HG00544.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1613-23T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 5/9 | chr1 | 117018133 | |||||||
chr1:117018638 | A | G | 2 | a0001c0003t0001g0337 a0001c0003t0001g0338 |
2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2017+78A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117018638 | |||||||
chr1:117018963 | T | A | 1 | a0001c0002t0001g0015 | 2 | HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2017+403T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117018963 | |||||||
chr1:117018992 | A | G | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2017+432A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117018992 | |||||||
chr1:117019172 | G | T | 5 | a0001c0002t0001g0022 a0001c0002t0001g0071 a0001c0002t0001g0086 others(2): Show |
6 | HG00738.hp2 HG02300.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+612G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019172 | |||||||
chr1:117019186 | C | T | 3 | a0006c0021t0001g0116 a0006c0021t0001g0117 a0029c0044t0001g0344 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2017+626C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019186 | |||||||
chr1:117019241 | A | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(223): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2017+681A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019241 | |||||||
chr1:117019347 | C | T | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2017+787C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019347 | |||||||
chr1:117019676 | C | A | 4 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(1): Show |
5 | HG02970.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017+1116C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019676 | |||||||
chr1:117019776 | C | T | 1 | a0003c0005t0001g0317 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2017+1216C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019776 | |||||||
chr1:117019815 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2017+1255T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019815 | |||||||
chr1:117019827 | T | C | 169 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0214 others(166): Show |
202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2017+1267T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117019827 | |||||||
chr1:117020093 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2018-1480A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020093 | |||||||
chr1:117020212 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2018-1361A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020212 | |||||||
chr1:117020218 | C | T | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2018-1355C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020218 | |||||||
chr1:117020234 | G | A | 5 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(2): Show |
5 | HG02738.hp2 HG03688.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1339G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020234 | |||||||
chr1:117020373 | G | A | 2 | a0005c0007t0001g0052 a0005c0007t0004g0326 |
3 | HG01884.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2018-1200G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020373 | |||||||
chr1:117020531 | A | G | 3 | a0001c0002t0001g0054 a0001c0002t0001g0109 a0019c0037t0001g0108 |
3 | HG00621.hp2 HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2018-1042A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020531 | |||||||
chr1:117020642 | A | G | 1 | a0004c0006t0001g0289 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2018-931A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020642 | |||||||
chr1:117020654 | C | T | 7 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(4): Show |
8 | HG01891.hp1 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2018-919C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020654 | |||||||
chr1:117020821 | G | A | 1 | a0002c0004t0001g0242 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2018-752G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020821 | |||||||
chr1:117020839 | A | G | 1 | a0007c0036t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2018-734A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020839 | |||||||
chr1:117020936 | G | C | 1 | a0001c0001t0001g0036 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2018-637G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020936 | |||||||
chr1:117020944 | A | C | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-629A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020944 | |||||||
chr1:117020947 | A | C | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-626A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020947 | |||||||
chr1:117020949 | A | C | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-624A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020949 | |||||||
chr1:117020951 | C | A | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-622C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020951 | |||||||
chr1:117020952 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-621T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020952 | |||||||
chr1:117020954 | C | A | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-619C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020954 | |||||||
chr1:117020959 | G | T | 1 | a0001c0002t0001g0085 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2018-614G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020959 | |||||||
chr1:117020960 | T | C | 159 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0001c0001t0001g0214 others(156): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2018-613T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117020960 | |||||||
chr1:117021246 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0230 others(5): Show |
10 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2018-327C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117021246 | |||||||
chr1:117021251 | C | A | 2 | a0002c0004t0001g0244 a0023c0041t0005g0243 |
2 | HG01361.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2018-322C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117021251 | |||||||
chr1:117021335 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2018-238G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117021335 | |||||||
chr1:117021451 | T | C | 1 | a0002c0004t0001g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2018-122T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117021451 | |||||||
chr1:117021479 | G | A | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2018-94G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117021479 | |||||||
chr1:117021538 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2018-35A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 6/9 | chr1 | 117021538 | |||||||
chr1:117022053 | T | G | 1 | a0001c0001t0002g0183 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2428+70T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022053 | |||||||
chr1:117022112 | T | A | 1 | a0004c0006t0001g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2428+129T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022112 | |||||||
chr1:117022268 | C | T | 137 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0017 others(134): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2428+285C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022268 | |||||||
chr1:117022287 | C | A | 148 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0001g0221 others(145): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2428+304C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022287 | |||||||
chr1:117022725 | C | T | 7 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(4): Show |
8 | HG01891.hp1 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2428+742C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022725 | |||||||
chr1:117022754 | T | C | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2428+771T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022754 | |||||||
chr1:117022786 | A | G | 1 | a0005c0007t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2428+803A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022786 | |||||||
chr1:117022793 | G | C | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG00099.hp1 HG01175.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2428+810G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117022793 | |||||||
chr1:117023122 | G | T | 1 | a0020c0024t0003g0332 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2428+1139G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023122 | |||||||
chr1:117023497 | A | G | 1 | a0001c0003t0001g0161 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2428+1514A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023497 | |||||||
chr1:117023559 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2428+1576G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023559 | |||||||
chr1:117023565 | T | C | 10 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2428+1582T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023565 | |||||||
chr1:117023571 | C | T | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2428+1588C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023571 | |||||||
chr1:117023579 | G | A | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2428+1596G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023579 | |||||||
chr1:117023597 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2428+1614A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023597 | |||||||
chr1:117023631 | G | A | 1 | a0001c0003t0001g0144 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2428+1648G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023631 | |||||||
chr1:117023758 | T | C | 5 | a0002c0004t0001g0037 a0002c0004t0001g0038 a0002c0004t0001g0246 others(2): Show |
7 | HG02135.hp2 NA18952.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2429-1751T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023758 | |||||||
chr1:117023796 | G | A | 2 | a0006c0021t0001g0116 a0006c0021t0001g0117 |
2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2429-1713G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117023796 | |||||||
chr1:117024023 | A | C | 1 | a0026c0032t0002g0228 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2429-1486A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024023 | |||||||
chr1:117024086 | T | C | 1 | a0001c0002t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2429-1423T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024086 | |||||||
chr1:117024202 | C | T | 1 | a0001c0002t0002g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2429-1307C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024202 | |||||||
chr1:117024302 | C | A | 1 | a0001c0002t0001g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2429-1207C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024302 | |||||||
chr1:117024391 | C | T | 1 | a0001c0003t0001g0336 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2429-1118C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024391 | |||||||
chr1:117024426 | A | G | 165 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0001g0221 others(162): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.2429-1083A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024426 | |||||||
chr1:117024431 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(305): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2429-1078T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024431 | |||||||
chr1:117024471 | C | T | 8 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(5): Show |
9 | HG01891.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2429-1038C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024471 | |||||||
chr1:117024494 | A | AAAAT | 3 | a0006c0021t0001g0116 a0006c0021t0001g0117 a0029c0044t0001g0344 |
3 | HG01891.hp1 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2429-986_2429-983d others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 117024494 | ||||||
chr1:117024494 | A | AAAATAAA others(1): Show |
5 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(2): Show |
6 | HG02647.hp2 HG02970.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2429-990_2429-983d others(10): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 117024494 | ||||||
chr1:117024494 | AAAAT | A | 330 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(327): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.2429-986_2429-983d others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 117024494 | ||||||
chr1:117024867 | T | C | 10 | a0006c0008t0001g0053 a0006c0008t0001g0339 a0006c0008t0001g0340 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2429-642T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024867 | |||||||
chr1:117024904 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(215): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.2429-605G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117024904 | |||||||
chr1:117025205 | A | T | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2429-304A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117025205 | |||||||
chr1:117025235 | C | T | 1 | a0001c0001t0004g0218 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2429-274C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117025235 | |||||||
chr1:117025236 | G | A | 1 | a0011c0026t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2429-273G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117025236 | |||||||
chr1:117025311 | T | C | 2 | a0013c0015t0001g0122 a0013c0015t0003g0121 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2429-198T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117025311 | |||||||
chr1:117025378 | T | TA | 5 | a0001c0002t0001g0054 a0001c0002t0001g0093 a0001c0002t0001g0096 others(2): Show |
5 | HG00408.hp1 HG00621.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2429-123dupA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 117025378 | ||||||
chr1:117025451 | G | T | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2429-58G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117025451 | |||||||
chr1:117025471 | G | T | 28 | a0003c0005t0001g0010 a0003c0005t0001g0043 a0003c0005t0001g0266 others(25): Show |
33 | HG00438.hp2 HG00621.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.2429-38G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 7/9 | chr1 | 117025471 | |||||||
chr1:117025992 | C | CCTT | 9 | a0001c0001t0003g0220 a0006c0008t0001g0053 a0006c0008t0001g0339 others(6): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2824+91_2824+93dup others(3): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117025992 | ||||||
chr1:117026110 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2824+206A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026110 | |||||||
chr1:117026126 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2824+222C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026126 | |||||||
chr1:117026156 | G | T | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2824+252G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026156 | |||||||
chr1:117026241 | T | C | 1 | a0001c0003t0001g0164 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2824+337T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026241 | |||||||
chr1:117026318 | T | C | 1 | a0003c0005t0001g0324 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2824+414T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026318 | |||||||
chr1:117026325 | G | C | 155 | a0001c0001t0001g0034 a0001c0001t0001g0120 a0001c0001t0001g0214 others(152): Show |
185 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.2824+421G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026325 | |||||||
chr1:117026353 | A | G | 1 | a0010c0030t0004g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2824+449A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026353 | |||||||
chr1:117026403 | G | C | 1 | a0001c0001t0003g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2824+499G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026403 | |||||||
chr1:117026435 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2824+531T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026435 | |||||||
chr1:117026687 | G | T | 1 | a0003c0005t0002g0316 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2824+783G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026687 | |||||||
chr1:117026689 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0120 a0001c0001t0003g0119 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2824+785G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026689 | |||||||
chr1:117026728 | A | G | 1 | a0001c0003t0001g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2824+824A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026728 | |||||||
chr1:117026768 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(213): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.2824+864C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026768 | |||||||
chr1:117026816 | C | G | 2 | a0001c0003t0001g0159 a0001c0003t0001g0173 |
2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2824+912C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026816 | |||||||
chr1:117026862 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0004g0218 a0001c0001t0004g0219 others(1): Show |
5 | HG02965.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2824+958T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026862 | |||||||
chr1:117026892 | G | A | 70 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0200 others(67): Show |
79 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.2824+988G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026892 | |||||||
chr1:117026908 | A | G | 1 | a0029c0044t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2824+1004A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026908 | |||||||
chr1:117026911 | T | A | 18 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0004g0218 others(15): Show |
20 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.2824+1007T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026911 | |||||||
chr1:117026971 | A | T | 4 | a0006c0008t0001g0339 a0006c0008t0001g0340 a0014c0029t0003g0262 others(1): Show |
4 | HG02280.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2824+1067A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026971 | |||||||
chr1:117026994 | T | A | 106 | a0001c0001t0001g0034 a0001c0001t0001g0180 a0001c0001t0001g0186 others(103): Show |
125 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.2824+1090T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117026994 | |||||||
chr1:117027051 | G | T | 15 | a0001c0001t0001g0034 a0001c0001t0002g0049 a0001c0001t0004g0213 others(12): Show |
20 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2824+1147G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027051 | |||||||
chr1:117027162 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0259 others(2): Show |
9 | NA18943.hp1 NA18950.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.2824+1258A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027162 | |||||||
chr1:117027175 | C | A | 9 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0003t0001g0033 others(6): Show |
10 | HG01433.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2824+1271C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027175 | |||||||
chr1:117027191 | C | T | 1 | a0001c0001t0003g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2824+1287C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027191 | |||||||
chr1:117027201 | A | G | 5 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0012c0014t0001g0342 others(2): Show |
5 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2824+1297A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027201 | |||||||
chr1:117027445 | G | A | 1 | a0003c0005t0001g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2824+1541G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027445 | |||||||
chr1:117027507 | A | G | 335 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(332): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.2824+1603A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027507 | |||||||
chr1:117027614 | G | C | 2 | a0001c0002t0001g0018 a0001c0002t0001g0077 |
3 | HG03490.hp1 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2824+1710G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027614 | |||||||
chr1:117027737 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2824+1833T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027737 | |||||||
chr1:117027806 | G | A | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2824+1902G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027806 | |||||||
chr1:117027820 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(11): Show |
18 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2824+1916G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027820 | |||||||
chr1:117027825 | T | A | 1 | a0001c0002t0001g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2824+1921T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027825 | |||||||
chr1:117027861 | G | A | 15 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(12): Show |
19 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2824+1957G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027861 | |||||||
chr1:117027870 | C | T | 190 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0041 others(187): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2824+1966C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027870 | |||||||
chr1:117027871 | G | A | 15 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(12): Show |
19 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2824+1967G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027871 | |||||||
chr1:117027941 | C | T | 3 | a0006c0008t0001g0339 a0006c0008t0001g0340 a0029c0044t0001g0344 |
3 | HG02970.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2824+2037C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027941 | |||||||
chr1:117027999 | C | T | 3 | a0010c0013t0004g0126 a0010c0013t0004g0129 a0010c0030t0004g0263 |
3 | HG03471.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2824+2095C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117027999 | |||||||
chr1:117028042 | G | A | 2 | a0001c0003t0001g0217 a0001c0003t0004g0178 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2824+2138G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028042 | |||||||
chr1:117028089 | A | C | 1 | a0002c0040t0001g0310 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2824+2185A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028089 | |||||||
chr1:117028102 | T | TA | 178 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0041 others(175): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2824+2201dupA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117028102 | ||||||
chr1:117028102 | T | TAAAATA | 14 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0002t0001g0066 others(11): Show |
14 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2824+2201_2824+220 others(10): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117028102 | ||||||
chr1:117028102 | T | TAAATAAA others(26): Show |
1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2824+2205_2824+220 others(37): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117028102 | ||||||
chr1:117028107 | A | AAATAAAT | 20 | a0001c0001t0001g0034 a0001c0001t0001g0250 a0001c0001t0001g0300 others(17): Show |
23 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2824+2205_2824+220 others(11): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117028107 | ||||||
chr1:117028107 | A | AAATAAAT others(4): Show |
3 | a0002c0004t0001g0244 a0005c0007t0001g0052 a0006c0021t0001g0116 |
4 | HG01361.hp1 HG01891.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2824+2205_2824+220 others(15): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117028107 | ||||||
chr1:117028124 | G | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(332): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.2824+2220G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028124 | |||||||
chr1:117028367 | G | A | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2824+2463G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028367 | |||||||
chr1:117028457 | G | C | 1 | a0006c0021t0001g0117 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2824+2553G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028457 | |||||||
chr1:117028457 | G | T | 36 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0185 others(33): Show |
39 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2824+2553G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028457 | |||||||
chr1:117028607 | G | T | 1 | a0001c0003t0002g0335 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2824+2703G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028607 | |||||||
chr1:117028624 | G | C | 2 | a0001c0002t0001g0098 a0001c0002t0001g0099 |
2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2824+2720G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028624 | |||||||
chr1:117028711 | G | T | 3 | a0010c0013t0004g0126 a0010c0013t0004g0129 a0010c0030t0004g0263 |
3 | HG03471.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2824+2807G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028711 | |||||||
chr1:117028959 | G | A | 8 | a0001c0001t0001g0221 a0001c0001t0003g0222 a0001c0010t0003g0123 others(5): Show |
9 | HG02280.hp1 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2824+3055G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117028959 | |||||||
chr1:117029022 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3118G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029022 | |||||||
chr1:117029024 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3120G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029024 | |||||||
chr1:117029025 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3121G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029025 | |||||||
chr1:117029032 | C | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3128C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029032 | |||||||
chr1:117029033 | C | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3129C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029033 | |||||||
chr1:117029036 | C | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3132C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029036 | |||||||
chr1:117029043 | AAAAG | A | 18 | a0001c0001t0001g0199 a0001c0003t0001g0007 a0001c0003t0001g0029 others(15): Show |
22 | HG00438.hp1 HG00673.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.2824+3149_2824+315 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029043 | ||||||
chr1:117029057 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3153G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029057 | |||||||
chr1:117029063 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3159G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029063 | |||||||
chr1:117029065 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3161G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029065 | |||||||
chr1:117029066 | A | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3162A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029066 | |||||||
chr1:117029069 | A | T | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3165A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029069 | |||||||
chr1:117029072 | G | A | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0002t0001g0115 others(1): Show |
4 | HG00099.hp1 HG02559.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2824+3168G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029072 | |||||||
chr1:117029075 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3171G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029075 | |||||||
chr1:117029080 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3176G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029080 | |||||||
chr1:117029087 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3183G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029087 | |||||||
chr1:117029089 | T | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3185T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029089 | |||||||
chr1:117029091 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3187G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029091 | |||||||
chr1:117029093 | T | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3189T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029093 | |||||||
chr1:117029094 | T | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3190T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029094 | |||||||
chr1:117029102 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3198G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029102 | |||||||
chr1:117029105 | T | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3201T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029105 | |||||||
chr1:117029107 | G | C | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3203G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029107 | |||||||
chr1:117029109 | T | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3205T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029109 | |||||||
chr1:117029115 | T | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3211T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029115 | |||||||
chr1:117029118 | C | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3214C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029118 | |||||||
chr1:117029121 | T | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3217T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029121 | |||||||
chr1:117029122 | C | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3218C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029122 | |||||||
chr1:117029123 | C | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3219C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029123 | |||||||
chr1:117029126 | C | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3222C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029126 | |||||||
chr1:117029128 | T | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3224T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029128 | |||||||
chr1:117029129 | C | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3225C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029129 | |||||||
chr1:117029129 | CAGAA | C | 18 | a0001c0001t0001g0225 a0001c0002t0001g0086 a0001c0002t0001g0087 others(15): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2824+3299_2824+330 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029129 | ||||||
chr1:117029129 | CAGAAAGA others(1): Show |
C | 11 | a0001c0001t0001g0187 a0001c0001t0001g0250 a0001c0002t0001g0022 others(8): Show |
12 | HG00738.hp2 HG01255.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.2824+3295_2824+330 others(12): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029129 | ||||||
chr1:117029129 | CAGAAAGA others(5): Show |
C | 3 | a0001c0001t0001g0209 a0001c0001t0004g0219 a0001c0003t0001g0165 |
3 | HG00558.hp2 HG03139.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2824+3291_2824+330 others(16): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029129 | ||||||
chr1:117029131 | GAAAGAAA others(75): Show |
G | 3 | a0001c0002t0001g0065 a0003c0005t0001g0325 a0005c0007t0001g0014 |
5 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.2824+3289_2824+337 others(86): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029131 | ||||||
chr1:117029135 | GAAAGAAA others(71): Show |
G | 3 | a0005c0007t0001g0328 a0005c0007t0001g0329 a0005c0007t0001g0330 |
3 | HG01109.hp1 HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2824+3293_2824+337 others(82): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029135 | ||||||
chr1:117029139 | GAAAGAAA others(67): Show |
G | 1 | a0002c0004t0001g0244 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2824+3297_2824+337 others(78): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029139 | ||||||
chr1:117029174 | A | G | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3270A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029174 | |||||||
chr1:117029175 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3271G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029175 | |||||||
chr1:117029179 | GAAAGAAA others(14): Show |
G | 2 | a0001c0001t0004g0241 a0010c0013t0004g0129 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2824+3278_2824+329 others(25): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029179 | ||||||
chr1:117029182 | A | G | 4 | a0001c0034t0003g0162 a0002c0004t0003g0048 a0012c0014t0001g0343 others(1): Show |
4 | HG02717.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2824+3278A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029182 | |||||||
chr1:117029183 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3279G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029183 | |||||||
chr1:117029183 | GAAAGAAA others(10): Show |
G | 5 | a0001c0001t0003g0184 a0001c0002t0001g0067 a0001c0003t0001g0005 others(2): Show |
5 | HG00323.hp2 HG02809.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.2824+3282_2824+329 others(21): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029183 | ||||||
chr1:117029184 | A | AAAGAAAG others(3): Show |
1 | a0004c0006t0001g0251 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2824+3289_2824+329 others(14): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029184 | ||||||
chr1:117029184 | AAAGAAAG others(66): Show |
A | 2 | a0001c0001t0001g0034 a0006c0021t0001g0116 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2824+3283_2824+335 others(77): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029184 | ||||||
chr1:117029186 | A | G | 5 | a0001c0002t0001g0020 a0001c0002t0001g0077 a0002c0004t0001g0290 others(2): Show |
5 | HG01261.hp1 HG01433.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2824+3282A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029186 | |||||||
chr1:117029187 | GAAAGAAA others(6): Show |
G | 9 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0002g0312 others(6): Show |
10 | HG00621.hp2 HG01168.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2824+3286_2824+329 others(17): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029187 | ||||||
chr1:117029188 | AAAGAAAG others(4): Show |
A | 1 | a0001c0002t0001g0057 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2824+3287_2824+329 others(15): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029188 | ||||||
chr1:117029188 | AAAGAAAG others(62): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2824+3287_2824+335 others(73): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029188 | ||||||
chr1:117029190 | A | G | 21 | a0001c0001t0001g0214 a0001c0001t0001g0287 a0001c0002t0001g0018 others(18): Show |
23 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.2824+3286A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029190 | |||||||
chr1:117029191 | GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2824+3299_2824+331 others(17): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029191 | ||||||
chr1:117029192 | AAAGAAAG others(18): Show |
A | 2 | a0001c0034t0003g0162 a0026c0032t0002g0228 |
2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2824+3291_2824+331 others(29): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029192 | ||||||
chr1:117029192 | AAAGAAAG others(26): Show |
A | 1 | a0002c0004t0003g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2824+3291_2824+332 others(37): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029192 | ||||||
chr1:117029192 | AAAGAAAG others(30): Show |
A | 1 | a0012c0014t0001g0343 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2824+3291_2824+332 others(41): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029192 | ||||||
chr1:117029192 | AAAGAAAG others(58): Show |
A | 2 | a0005c0007t0001g0052 a0015c0019t0001g0135 |
2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2824+3291_2824+335 others(69): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029192 | ||||||
chr1:117029194 | A | AGAAAGAA others(13): Show |
2 | a0001c0001t0001g0204 a0001c0003t0004g0178 |
2 | HG01952.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2824+3302_2824+330 others(24): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029194 | ||||||
chr1:117029194 | A | AGAAAGAA others(9): Show |
6 | a0001c0001t0001g0041 a0001c0001t0001g0233 a0001c0001t0001g0238 others(3): Show |
6 | HG00735.hp1 HG02074.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824+3302_2824+330 others(20): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029194 | ||||||
chr1:117029194 | A | AGAAAGAA others(5): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0197 a0002c0004t0001g0012 others(2): Show |
6 | HG01515.hp2 HG03942.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824+3301_2824+330 others(16): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029194 | ||||||
chr1:117029194 | A | AGAAAGAA others(1): Show |
6 | a0001c0001t0001g0180 a0001c0001t0001g0192 a0001c0003t0001g0006 others(3): Show |
6 | HG00323.hp1 HG02135.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824+3297_2824+329 others(12): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029194 | ||||||
chr1:117029194 | A | AGAAAGAA others(4): Show |
1 | a0004c0006t0001g0008 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2824+3297_2824+329 others(15): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029194 | ||||||
chr1:117029194 | A | AGAAG | 14 | a0001c0001t0001g0185 a0001c0001t0003g0215 a0001c0002t0001g0073 others(11): Show |
18 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.2824+3293_2824+329 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029194 | ||||||
chr1:117029194 | A | G | 98 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(95): Show |
119 | HG00544.hp2 HG00639.hp2 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.2824+3290A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029194 | |||||||
chr1:117029195 | GAAAGA | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0221 others(44): Show |
52 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2824+3294_2824+329 others(9): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029195 | ||||||
chr1:117029195 | GAAAGAAA others(11): Show |
G | 1 | a0008c0009t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2824+3303_2824+332 others(22): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029195 | ||||||
chr1:117029196 | AAAGAAAG others(14): Show |
A | 1 | a0027c0042t0001g0279 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2824+3295_2824+331 others(25): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029196 | ||||||
chr1:117029196 | AAAGAAAG others(18): Show |
A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0077 |
2 | HG03831.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2824+3295_2824+331 others(29): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029196 | ||||||
chr1:117029196 | AAAGAAAG others(22): Show |
A | 1 | a0025c0025t0003g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2824+3295_2824+332 others(33): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029196 | ||||||
chr1:117029196 | AAAGAAAG others(26): Show |
A | 1 | a0012c0014t0001g0342 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2824+3295_2824+332 others(37): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029196 | ||||||
chr1:117029196 | AAAGAAAG others(54): Show |
A | 2 | a0001c0001t0001g0300 a0005c0007t0001g0052 |
2 | HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2824+3295_2824+335 others(65): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029196 | ||||||
chr1:117029198 | A | G | 25 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0199 others(22): Show |
26 | HG00438.hp1 HG00639.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.2824+3294A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029198 | |||||||
chr1:117029199 | GA | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0120 others(38): Show |
43 | HG00099.hp2 HG00597.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.2824+3298delA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029199 | ||||||
chr1:117029199 | GAAAGAAA others(3): Show |
G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0210 |
2 | NA18953.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2824+3298_2824+330 others(14): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029199 | ||||||
chr1:117029200 | A | AAGGAAAG others(46): Show |
1 | a0002c0004t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2824+3297_2824+329 others(57): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029200 | AAAGAAAA others(10): Show |
A | 6 | a0001c0001t0001g0287 a0001c0002t0001g0098 a0001c0002t0001g0110 others(3): Show |
6 | HG01496.hp2 HG01928.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2824+3299_2824+331 others(21): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029200 | AAAGAAAA others(14): Show |
A | 8 | a0001c0001t0001g0214 a0001c0002t0001g0018 a0001c0002t0001g0020 others(5): Show |
10 | HG01168.hp1 HG01169.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2824+3299_2824+331 others(25): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029200 | AAAGAAAA others(18): Show |
A | 3 | a0001c0002t0001g0085 a0001c0010t0003g0128 a0002c0004t0003g0048 |
3 | HG01934.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2824+3299_2824+332 others(29): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029200 | AAAGAAAA others(22): Show |
A | 2 | a0001c0002t0001g0099 a0005c0007t0001g0327 |
2 | HG01952.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2824+3299_2824+332 others(33): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029200 | AAAGAAAA others(26): Show |
A | 1 | a0001c0002t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2824+3299_2824+333 others(37): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029200 | AAAGAAAA others(50): Show |
A | 2 | a0001c0031t0006g0240 a0024c0027t0001g0133 |
2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2824+3299_2824+335 others(61): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029200 | ||||||
chr1:117029201 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2824+3297A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029201 | |||||||
chr1:117029202 | A | G | 1 | a0001c0003t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2824+3298A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029202 | |||||||
chr1:117029203 | GA | G | 11 | a0001c0001t0001g0315 a0001c0001t0001g0323 a0001c0002t0002g0063 others(8): Show |
12 | HG00099.hp1 HG00544.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.2824+3303delA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029203 | ||||||
chr1:117029203 | GAAAAGAA others(3): Show |
G | 2 | a0001c0002t0001g0068 a0001c0003t0001g0144 |
2 | HG02015.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.2824+3303_2824+331 others(14): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029203 | ||||||
chr1:117029204 | A | AAAG | 3 | a0001c0003t0001g0007 a0001c0003t0001g0029 a0001c0003t0001g0171 |
4 | HG02135.hp1 NA18948.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2824+3302_2824+330 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0009 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2824+3302_2824+330 others(23): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAAGAAAG others(4): Show |
2 | a0001c0003t0001g0177 a0003c0005t0001g0277 |
2 | NA18949.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2824+3302_2824+330 others(15): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAAGAAGG | 10 | a0001c0001t0001g0042 a0001c0001t0001g0306 a0001c0002t0002g0112 others(7): Show |
12 | HG02040.hp1 HG03453.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.2824+3302_2824+330 others(11): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAAGAAGG others(8): Show |
1 | a0001c0003t0001g0151 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2824+3302_2824+330 others(19): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAGG | 21 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0042 others(18): Show |
22 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2824+3301_2824+330 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAGGAAAG others(54): Show |
1 | a0002c0004t0001g0044 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2824+3301_2824+330 others(65): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | AAGGAAAG others(4): Show |
1 | a0001c0003t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2824+3301_2824+330 others(15): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0036 others(101): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2824+3300A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029204 | |||||||
chr1:117029204 | AAAAGAAA others(10): Show |
A | 3 | a0001c0001t0001g0211 a0001c0002t0001g0070 a0001c0003t0001g0028 |
3 | NA18747.hp1 NA18965.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2824+3312_2824+332 others(21): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029204 | AAAAGAAA others(14): Show |
A | 2 | a0001c0002t0001g0114 a0002c0004t0001g0284 |
2 | HG00544.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2824+3312_2824+333 others(25): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029204 | ||||||
chr1:117029206 | AAG | A | 3 | a0011c0016t0001g0091 a0013c0015t0001g0122 a0020c0024t0003g0332 |
3 | HG02257.hp1 HG02723.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2824+3304_2824+330 others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029206 | ||||||
chr1:117029207 | A | G | 31 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0227 others(28): Show |
36 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2824+3303A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029207 | |||||||
chr1:117029208 | G | A | 18 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0227 others(15): Show |
19 | HG00639.hp1 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2824+3304G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029208 | |||||||
chr1:117029209 | A | G | 3 | a0011c0016t0001g0091 a0013c0015t0001g0122 a0020c0024t0003g0332 |
3 | HG02257.hp1 HG02723.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2824+3305A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029209 | |||||||
chr1:117029212 | G | A | 1 | a0002c0004t0001g0292 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2824+3308G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029212 | |||||||
chr1:117029213 | A | AAAAG | 7 | a0001c0001t0001g0185 a0001c0001t0002g0260 a0001c0002t0001g0073 others(4): Show |
9 | HG00323.hp1 HG01884.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2824+3367_2824+337 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | A | AAAG | 3 | a0001c0001t0001g0009 a0002c0004t0001g0290 a0002c0004t0001g0292 |
3 | HG01167.hp1 HG01261.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.2824+3311_2824+331 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | A | G | 7 | a0001c0001t0001g0140 a0001c0001t0001g0210 a0001c0002t0001g0021 others(4): Show |
7 | HG02257.hp1 HG02723.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.2824+3309A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029213 | |||||||
chr1:117029213 | AAAAG | A | 23 | a0001c0001t0001g0187 a0001c0001t0001g0196 a0001c0001t0001g0225 others(20): Show |
28 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.2824+3367_2824+337 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | AAAAGAAA others(1): Show |
A | 38 | a0001c0001t0001g0188 a0001c0001t0001g0199 a0001c0001t0001g0200 others(35): Show |
43 | HG00438.hp1 HG00558.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.2824+3363_2824+337 others(12): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | AAAAGAAA others(5): Show |
A | 16 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0186 others(13): Show |
17 | HG01934.hp1 HG01978.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.2824+3359_2824+337 others(16): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | AAAAGAAA others(9): Show |
A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0208 others(7): Show |
11 | HG00735.hp2 HG00738.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.2824+3355_2824+337 others(20): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | AAAAGAAA others(13): Show |
A | 4 | a0001c0001t0003g0220 a0001c0002t0001g0003 a0001c0002t0001g0024 others(1): Show |
5 | HG01258.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2824+3351_2824+337 others(24): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029213 | AAAAGAAA others(17): Show |
A | 4 | a0001c0001t0003g0119 a0001c0002t0001g0024 a0001c0010t0003g0124 others(1): Show |
4 | HG01261.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2824+3347_2824+337 others(28): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029213 | ||||||
chr1:117029216 | A | G | 28 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0227 others(25): Show |
29 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.2824+3312A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029216 | |||||||
chr1:117029217 | G | A | 27 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0227 others(24): Show |
28 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2824+3313G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029217 | |||||||
chr1:117029217 | G | GAAAGA | 23 | a0001c0001t0001g0042 a0001c0001t0001g0190 a0001c0001t0001g0195 others(20): Show |
25 | HG00099.hp2 HG00673.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.2824+3316_2824+332 others(9): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029217 | ||||||
chr1:117029217 | G | GAAAGAAA others(47): Show |
1 | a0002c0004t0001g0047 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2824+3347_2824+334 others(58): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029217 | ||||||
chr1:117029221 | G | GA | 45 | a0001c0001t0001g0009 a0001c0001t0001g0202 a0001c0001t0001g0230 others(42): Show |
52 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.2824+3320dupA | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029221 | ||||||
chr1:117029221 | G | GAAAGAAA others(47): Show |
1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2824+3351_2824+335 others(58): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029221 | ||||||
chr1:117029222 | AAAG | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0036 others(41): Show |
59 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2824+3321_2824+332 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029222 | ||||||
chr1:117029222 | AAAGAAAG | A | 24 | a0001c0001t0001g0120 a0001c0001t0001g0137 a0001c0001t0001g0191 others(21): Show |
25 | HG00597.hp1 HG01074.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.2824+3321_2824+332 others(11): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029222 | ||||||
chr1:117029222 | AAAGAAAG others(4): Show |
A | 7 | a0001c0001t0003g0203 a0001c0002t0001g0023 a0001c0002t0001g0094 others(4): Show |
8 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.2824+3321_2824+333 others(15): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029222 | ||||||
chr1:117029222 | AAAGAAAG others(8): Show |
A | 3 | a0001c0001t0001g0221 a0001c0001t0003g0222 a0001c0010t0003g0123 |
3 | HG02818.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2824+3321_2824+333 others(19): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029222 | ||||||
chr1:117029225 | G | GAAAGAAA others(43): Show |
1 | a0002c0004t0001g0046 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2824+3351_2824+335 others(54): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029225 | ||||||
chr1:117029225 | G | GAAAGAAA others(27): Show |
1 | a0002c0004t0001g0290 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2824+3335_2824+333 others(38): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029225 | ||||||
chr1:117029226 | AAAG | A | 15 | a0001c0001t0001g0287 a0001c0001t0001g0315 a0001c0001t0001g0323 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.2824+3325_2824+332 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029226 | ||||||
chr1:117029230 | AAAG | A | 10 | a0001c0001t0001g0214 a0001c0002t0001g0018 a0001c0002t0001g0020 others(7): Show |
13 | HG01168.hp1 HG01169.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2824+3329_2824+333 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029230 | ||||||
chr1:117029234 | AAAG | A | 5 | a0001c0002t0001g0085 a0001c0010t0003g0128 a0002c0004t0003g0048 others(2): Show |
6 | HG01934.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824+3333_2824+333 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029234 | ||||||
chr1:117029238 | AAAG | A | 3 | a0005c0007t0001g0327 a0012c0014t0001g0342 a0012c0014t0001g0343 |
3 | HG01433.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2824+3337_2824+333 others(7): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029238 | ||||||
chr1:117029240 | A | AGAAAGAA others(44): Show |
1 | a0002c0004t0001g0044 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2824+3347_2824+334 others(55): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029240 | ||||||
chr1:117029282 | C | T | 1 | a0005c0007t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2824+3378C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029282 | |||||||
chr1:117029284 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(11): Show |
18 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2824+3380G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029284 | |||||||
chr1:117029285 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(148): Show |
178 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.2824+3381T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029285 | |||||||
chr1:117029288 | A | G | 1 | a0001c0003t0001g0139 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2824+3384A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029288 | |||||||
chr1:117029314 | GAAGA | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0188 others(5): Show |
11 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.2824+3424_2824+342 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117029314 | ||||||
chr1:117029615 | G | T | 1 | a0008c0009t0001g0016 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2824+3711G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029615 | |||||||
chr1:117029751 | C | T | 1 | a0005c0007t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2824+3847C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029751 | |||||||
chr1:117029756 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0188 |
3 | HG00733.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2824+3852C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029756 | |||||||
chr1:117029811 | T | C | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2824+3907T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117029811 | |||||||
chr1:117030105 | T | C | 29 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0185 others(26): Show |
32 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.2825-3755T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030105 | |||||||
chr1:117030160 | T | C | 2 | a0012c0014t0001g0342 a0012c0014t0001g0343 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2825-3700T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030160 | |||||||
chr1:117030377 | T | C | 1 | a0001c0001t0004g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2825-3483T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030377 | |||||||
chr1:117030379 | A | AAAAC | 3 | a0006c0008t0001g0339 a0006c0008t0001g0340 a0029c0044t0001g0344 |
3 | HG02970.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2825-3457_2825-345 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117030379 | ||||||
chr1:117030379 | A | AAAACAAA others(1): Show |
87 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0001g0180 others(84): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2825-3461_2825-345 others(12): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117030379 | ||||||
chr1:117030379 | A | AAAACAAA others(5): Show |
9 | a0001c0003t0001g0172 a0001c0003t0001g0229 a0002c0004t0001g0244 others(6): Show |
9 | HG01361.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2825-3465_2825-345 others(16): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117030379 | ||||||
chr1:117030379 | A | AAAACAAA others(9): Show |
1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2825-3469_2825-345 others(20): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117030379 | ||||||
chr1:117030379 | AAAAC | A | 5 | a0001c0001t0001g0208 a0001c0001t0002g0183 a0001c0002t0001g0102 others(2): Show |
5 | HG00738.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2825-3457_2825-345 others(8): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117030379 | ||||||
chr1:117030405 | A | AAG | 3 | a0001c0001t0001g0179 a0001c0001t0001g0306 a0005c0007t0004g0326 |
3 | HG01884.hp2 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2825-3441_2825-344 others(6): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 117030405 | ||||||
chr1:117030407 | G | C | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2825-3453G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030407 | |||||||
chr1:117030457 | A | G | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2825-3403A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030457 | |||||||
chr1:117030458 | G | A | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2825-3402G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030458 | |||||||
chr1:117030551 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(148): Show |
178 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.2825-3309T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030551 | |||||||
chr1:117030632 | T | G | 8 | a0001c0001t0003g0119 a0005c0007t0001g0327 a0010c0013t0004g0126 others(5): Show |
8 | HG01433.hp2 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2825-3228T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030632 | |||||||
chr1:117030710 | T | C | 3 | a0001c0001t0001g0250 a0001c0001t0003g0184 a0001c0034t0003g0162 |
3 | HG02809.hp1 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2825-3150T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117030710 | |||||||
chr1:117031051 | T | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(11): Show |
18 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2825-2809T>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031051 | |||||||
chr1:117031054 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2825-2806C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031054 | |||||||
chr1:117031064 | T | C | 1 | a0001c0001t0004g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2825-2796T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031064 | |||||||
chr1:117031151 | A | G | 3 | a0003c0005t0001g0010 a0003c0005t0001g0268 a0003c0005t0001g0269 |
6 | HG00621.hp1 NA18990.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.2825-2709A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031151 | |||||||
chr1:117031190 | G | C | 10 | a0001c0001t0001g0250 a0001c0001t0001g0301 a0001c0001t0003g0184 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2825-2670G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031190 | |||||||
chr1:117031347 | C | T | 1 | a0002c0004t0001g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2825-2513C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031347 | |||||||
chr1:117031401 | A | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(148): Show |
179 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.2825-2459A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031401 | |||||||
chr1:117031503 | G | A | 2 | a0001c0001t0003g0119 a0005c0007t0001g0327 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2825-2357G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031503 | |||||||
chr1:117031857 | T | C | 10 | a0001c0001t0001g0250 a0001c0001t0001g0301 a0001c0001t0003g0184 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2825-2003T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031857 | |||||||
chr1:117031869 | T | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(11): Show |
18 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2825-1991T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031869 | |||||||
chr1:117031899 | C | G | 83 | a0001c0001t0001g0140 a0001c0001t0001g0180 a0001c0001t0001g0186 others(80): Show |
105 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2825-1961C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031899 | |||||||
chr1:117031976 | C | T | 7 | a0001c0002t0001g0021 a0001c0002t0001g0058 a0001c0002t0001g0068 others(4): Show |
9 | HG00544.hp2 HG02015.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.2825-1884C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117031976 | |||||||
chr1:117032008 | G | A | 17 | a0001c0001t0001g0221 a0001c0001t0003g0222 a0001c0002t0001g0065 others(14): Show |
20 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2825-1852G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032008 | |||||||
chr1:117032027 | C | T | 1 | a0002c0004t0001g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2825-1833C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032027 | |||||||
chr1:117032028 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(79): Show |
103 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.2825-1832A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032028 | |||||||
chr1:117032038 | A | T | 2 | a0001c0002t0001g0018 a0001c0002t0001g0077 |
3 | HG03490.hp1 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2825-1822A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032038 | |||||||
chr1:117032177 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2825-1683C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032177 | |||||||
chr1:117032237 | A | C | 1 | a0001c0001t0003g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2825-1623A>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032237 | |||||||
chr1:117032353 | G | C | 3 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0015c0019t0002g0134 |
3 | HG02622.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2825-1507G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032353 | |||||||
chr1:117032391 | C | G | 7 | a0001c0002t0001g0065 a0002c0004t0001g0244 a0003c0005t0001g0325 others(4): Show |
9 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.2825-1469C>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032391 | |||||||
chr1:117032442 | A | G | 2 | a0001c0001t0001g0187 a0001c0003t0001g0132 |
2 | HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2825-1418A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032442 | |||||||
chr1:117032818 | C | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(10): Show |
17 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.2825-1042C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032818 | |||||||
chr1:117032887 | T | G | 1 | a0003c0005t0001g0298 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2825-973T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117032887 | |||||||
chr1:117033128 | T | C | 5 | a0001c0001t0003g0119 a0005c0007t0001g0327 a0013c0015t0001g0122 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2825-732T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033128 | |||||||
chr1:117033134 | C | T | 1 | a0005c0007t0001g0052 | 2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2825-726C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033134 | |||||||
chr1:117033240 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2825-620G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033240 | |||||||
chr1:117033342 | C | T | 11 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0002t0001g0065 others(8): Show |
15 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2825-518C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033342 | |||||||
chr1:117033434 | G | A | 1 | a0003c0005t0002g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2825-426G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033434 | |||||||
chr1:117033461 | A | G | 14 | a0001c0001t0001g0250 a0001c0001t0001g0301 a0001c0001t0003g0184 others(11): Show |
14 | HG01433.hp2 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2825-399A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033461 | |||||||
chr1:117033795 | T | C | 2 | a0001c0001t0003g0119 a0005c0007t0001g0327 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2825-65T>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 8/9 | chr1 | 117033795 | |||||||
chr1:117034236 | G | A | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*33+102G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117034236 | |||||||
chr1:117034306 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*33+172C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117034306 | |||||||
chr1:117034307 | G | A | 1 | a0014c0023t0003g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*33+173G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117034307 | |||||||
chr1:117034669 | A | G | 29 | a0001c0001t0002g0049 a0001c0001t0002g0312 a0001c0001t0004g0118 others(26): Show |
32 | HG00099.hp2 HG00544.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.*33+535A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117034669 | |||||||
chr1:117034801 | G | T | 24 | a0001c0001t0002g0049 a0001c0001t0002g0312 a0001c0001t0004g0218 others(21): Show |
27 | HG00099.hp2 HG00544.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.*33+667G>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117034801 | |||||||
chr1:117034936 | G | C | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*33+802G>C | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117034936 | |||||||
chr1:117035062 | CCTATT | C | 29 | a0001c0001t0002g0049 a0001c0001t0002g0194 a0001c0001t0002g0260 others(26): Show |
32 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.*33+931_*33+935del others(5): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 117035062 | ||||||
chr1:117035088 | G | A | 1 | a0001c0003t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.*33+954G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035088 | |||||||
chr1:117035116 | C | A | 29 | a0001c0001t0002g0049 a0001c0001t0002g0194 a0001c0001t0002g0260 others(26): Show |
32 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.*33+982C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035116 | |||||||
chr1:117035220 | A | AC | 29 | a0001c0001t0002g0049 a0001c0001t0002g0194 a0001c0001t0002g0260 others(26): Show |
32 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.*34-948_*34-947ins others(1): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035220 | |||||||
chr1:117035229 | G | A | 1 | a0001c0003t0001g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*34-939G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035229 | |||||||
chr1:117035237 | A | G | 3 | a0005c0007t0001g0327 a0013c0015t0001g0122 a0015c0019t0001g0135 |
3 | HG02723.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.*34-931A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035237 | |||||||
chr1:117035239 | C | A | 1 | a0015c0019t0002g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*34-929C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035239 | |||||||
chr1:117035321 | A | G | 1 | a0001c0002t0001g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.*34-847A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035321 | |||||||
chr1:117035362 | C | CCTTCCTA others(16): Show |
1 | a0001c0001t0002g0183 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*34-803_*34-781dup others(23): Show |
CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 117035362 | ||||||
chr1:117035367 | C | A | 2 | a0005c0007t0001g0327 a0013c0015t0001g0122 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.*34-801C>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035367 | |||||||
chr1:117035549 | C | CT | 11 | a0001c0001t0001g0196 a0001c0001t0001g0226 a0001c0002t0001g0081 others(8): Show |
11 | HG01346.hp2 HG02004.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.*34-601dupT | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 117035549 | ||||||
chr1:117035549 | CT | C | 41 | a0001c0001t0001g0197 a0001c0001t0001g0221 a0001c0001t0002g0049 others(38): Show |
45 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.*34-601delT | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 117035549 | ||||||
chr1:117035593 | G | A | 33 | a0001c0001t0002g0049 a0001c0001t0002g0194 a0001c0001t0002g0260 others(30): Show |
39 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.*34-575G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035593 | |||||||
chr1:117035643 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.*34-525G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035643 | |||||||
chr1:117035773 | C | T | 3 | a0001c0001t0002g0183 a0002c0004t0002g0308 a0002c0004t0002g0309 |
3 | HG02615.hp2 HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.*34-395C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035773 | |||||||
chr1:117035798 | C | T | 1 | a0001c0034t0003g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*34-370C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035798 | |||||||
chr1:117035831 | C | T | 1 | a0022c0043t0003g0239 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*34-337C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035831 | |||||||
chr1:117035842 | A | G | 1 | a0001c0003t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.*34-326A>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035842 | |||||||
chr1:117035847 | C | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0230 a0001c0001t0001g0286 others(4): Show |
8 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.*34-321C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035847 | |||||||
chr1:117035848 | G | A | 1 | a0001c0031t0006g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*34-320G>A | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117035848 | |||||||
chr1:117036038 | T | G | 2 | a0001c0003t0001g0028 a0001c0003t0001g0164 |
3 | NA18747.hp1 NA18960.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.*34-130T>G | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117036038 | |||||||
chr1:117036128 | C | T | 29 | a0001c0001t0002g0049 a0001c0001t0002g0183 a0001c0001t0002g0194 others(26): Show |
32 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.*34-40C>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117036128 | |||||||
chr1:117036141 | A | T | 29 | a0001c0001t0002g0049 a0001c0001t0002g0183 a0001c0001t0002g0194 others(26): Show |
32 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.*34-27A>T | CD101 | ENSG00000134256.13 | transcript | ENST00000682167.1 | protein_coding | 9/9 | chr1 | 117036141 |