Item | Value |
---|---|
geneid | 3619 |
ensemblid | ENSG00000149503.13 |
hgncid | 6058 |
symbol | INCENP |
name | inner centromere protein |
refseq_nuc | NM_001040694.2 |
refseq_prot | NP_001035784.1 |
ensembl_nuc | ENST00000394818.8 |
ensembl_prot | ENSP00000378295.3 |
mane_status | MANE Select |
chr | chr11 |
start | 62124011 |
end | 62153169 |
strand | + |
ver | v1.2 |
region | chr11:62124011-62153169 |
region5000 | chr11:62119011-62158169 |
regionname0 | INCENP_chr11_62124011_62153169 |
regionname5000 | INCENP_chr11_62119011_62158169 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 918 | 217 | 31 | 38 | 117 | 7 | 23 | 93 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0002 | 0/1 | 918 | 45 | 9 | 13 | 16 | 3 | 3 | 14 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0003 | 0/0 | 918 | 33 | 6 | 13 | 6 | 5 | 3 | 4 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0004 | 0/0 | 923 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(918): Show |
chr11 | 62119011 | 62158169 |
a0005 | 0/0 | 918 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MVTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0006 | 0/0 | 918 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0007 | 0/0 | 918 | 4 | 2 | 1 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0008 | 0/0 | 918 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0009 | 0/0 | 918 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0010 | 0/0 | 918 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0011 | 0/0 | 918 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0012 | 0/0 | 918 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0013 | 0/0 | 908 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(903): Show |
chr11 | 62119011 | 62158169 |
a0014 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0015 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0016 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0017 | 0/0 | 923 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MVTTA others(918): Show |
chr11 | 62119011 | 62158169 |
a0018 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0019 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0020 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0021 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0022 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0023 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
a0024 | 0/0 | 918 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | MGTTA others(913): Show |
chr11 | 62119011 | 62158169 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2754 | 94 | 19 | 11 | 49 | 4 | 11 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0002 | 1/0 | 2754 | 87 | 5 | 6 | 65 | 3 | 7 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0006 | 0/0 | 2754 | 10 | 0 | 10 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0007 | 0/0 | 2754 | 10 | 0 | 6 | 0 | 0 | 4 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0010 | 0/0 | 2754 | 6 | 3 | 3 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0017 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0018 | 0/0 | 2754 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0022 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0023 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0024 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0035 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0036 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0001c0038 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0002c0003 | 0/1 | 2754 | 45 | 9 | 13 | 16 | 3 | 3 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0003c0004 | 0/0 | 2754 | 31 | 6 | 11 | 6 | 5 | 3 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0003c0019 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0004c0005 | 0/0 | 2769 | 13 | 12 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2764): Show |
chr11 | 62119011 | 62158169 | ||
a0005c0008 | 0/0 | 2754 | 9 | 9 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGT others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0005c0020 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGT others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0006c0009 | 0/0 | 2754 | 6 | 6 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0007c0014 | 0/0 | 2754 | 3 | 2 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0007c0026 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0008c0012 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0009c0011 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0010c0015 | 0/0 | 2754 | 3 | 0 | 2 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0011c0013 | 0/0 | 2754 | 3 | 3 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0012c0031 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0012c0039 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0013c0016 | 0/0 | 2724 | 2 | 0 | 0 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2719): Show |
chr11 | 62119011 | 62158169 | ||
a0014c0021 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0015c0027 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0016c0037 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0017c0040 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGT others(2764): Show |
chr11 | 62119011 | 62158169 | ||
a0018c0032 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0019c0033 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0020c0029 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0021c0034 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0022c0028 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0023c0025 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 | ||
a0024c0030 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATGGG others(2749): Show |
chr11 | 62119011 | 62158169 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4114 | 94 | 19 | 11 | 49 | 4 | 11 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0002t0001 | 1/0 | 4114 | 86 | 5 | 6 | 64 | 3 | 7 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0002t0008 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0006t0001 | 0/0 | 4114 | 10 | 0 | 10 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0007t0001 | 0/0 | 4114 | 7 | 0 | 5 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0007t0006 | 0/0 | 4114 | 3 | 0 | 1 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0010t0001 | 0/0 | 4114 | 3 | 3 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0010t0005 | 0/0 | 4114 | 3 | 0 | 3 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0017t0004 | 0/0 | 4114 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0018t0001 | 0/0 | 4114 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0022t0001 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0023t0001 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0024t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0035t0001 | 0/0 | 4114 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0036t0001 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0001c0038t0001 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0002c0003t0002 | 0/0 | 4114 | 41 | 9 | 12 | 15 | 2 | 3 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0002c0003t0003 | 0/1 | 4114 | 3 | 0 | 1 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0002c0003t0010 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0003c0004t0002 | 0/0 | 4114 | 5 | 3 | 0 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0003c0004t0003 | 0/0 | 4114 | 26 | 3 | 11 | 6 | 5 | 1 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0003c0019t0003 | 0/0 | 4114 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0004c0005t0001 | 0/0 | 4129 | 12 | 11 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4124): Show |
chr11 | 62119011 | 62158169 |
a0004c0005t0011 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4124): Show |
chr11 | 62119011 | 62158169 |
a0005c0008t0004 | 0/0 | 4114 | 9 | 9 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0005c0020t0004 | 0/0 | 4114 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0006c0009t0001 | 0/0 | 4114 | 6 | 6 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0007c0014t0001 | 0/0 | 4114 | 3 | 2 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0007c0026t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0008c0012t0001 | 0/0 | 4114 | 4 | 4 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0009c0011t0001 | 0/0 | 4114 | 4 | 4 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0010c0015t0005 | 0/0 | 4114 | 3 | 0 | 2 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0011c0013t0001 | 0/0 | 4114 | 3 | 3 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0012c0031t0009 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0012c0039t0005 | 0/0 | 4114 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0013c0016t0001 | 0/0 | 4084 | 2 | 0 | 0 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4079): Show |
chr11 | 62119011 | 62158169 |
a0014c0021t0001 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0015c0027t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0016c0037t0002 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0017c0040t0007 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4124): Show |
chr11 | 62119011 | 62158169 |
a0018c0032t0001 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0019c0033t0001 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0020c0029t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0021c0034t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0022c0028t0001 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0023c0025t0001 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
a0024c0030t0001 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | ATAGT others(4109): Show |
chr11 | 62119011 | 62158169 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 19 | 0 | 3 | 13 | 1 | 2 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0002 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0004 | 0/0 | 14 | 0 | 0 | 9 | 0 | 5 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0006t0001g0005 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0007t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0007t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0007t0006g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0007t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0010t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0010t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0010t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0010t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0010t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0017t0004g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0018t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0018t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0022t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0023t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0024t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0035t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0036t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0001c0038t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0003 | 0/0 | 16 | 5 | 9 | 0 | 1 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0003g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0002c0003t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0012 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0019 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0004t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0019t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0003c0019t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0004c0005t0001g0006 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0004c0005t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0004c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0004c0005t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0005c0008t0004g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0005c0008t0004g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0005c0008t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0005c0020t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0006c0009t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0006c0009t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0006c0009t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0006c0009t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0006c0009t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0007c0014t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0007c0014t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0007c0026t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0008c0012t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0008c0012t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0009c0011t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0009c0011t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0010c0015t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0010c0015t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0011c0013t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0011c0013t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0012c0031t0009g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0012c0039t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0013c0016t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0014c0021t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0015c0027t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0016c0037t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0017c0040t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0018c0032t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0019c0033t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0020c0029t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0021c0034t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0022c0028t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0023c0025t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
a0024c0030t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0003 | g0012 | EUR | GBR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00140 | hp2 | a0002 | c0003 | t0002 | g0003 | EUR | GBR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0137 | EUR | FIN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00280 | hp2 | a0002 | c0003 | t0002 | g0048 | EUR | FIN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0136 | EUR | FIN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0032 | EUR | FIN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00597 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00639 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00639 | hp2 | a0003 | c0004 | t0003 | g0012 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00642 | hp2 | a0001 | c0036 | t0001 | g0080 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00673 | hp1 | a0003 | c0004 | t0003 | g0013 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00735 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00741 | hp1 | a0002 | c0003 | t0003 | g0013 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG00741 | hp2 | a0003 | c0004 | t0003 | g0046 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01069 | hp1 | a0001 | c0010 | t0005 | g0026 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01070 | hp1 | a0001 | c0007 | t0001 | g0041 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01070 | hp2 | a0001 | c0006 | t0001 | g0005 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01071 | hp1 | a0001 | c0010 | t0005 | g0026 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01071 | hp2 | a0001 | c0007 | t0001 | g0041 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01074 | hp1 | a0001 | c0010 | t0005 | g0056 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01081 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01081 | hp2 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01106 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01106 | hp2 | a0007 | c0014 | t0001 | g0025 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01109 | hp1 | a0012 | c0031 | t0009 | g0178 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01109 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01168 | hp1 | a0010 | c0015 | t0005 | g0024 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01168 | hp2 | a0003 | c0004 | t0003 | g0012 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01169 | hp1 | a0010 | c0015 | t0005 | g0024 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01169 | hp2 | a0003 | c0004 | t0003 | g0012 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01175 | hp2 | a0001 | c0006 | t0001 | g0005 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01192 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01255 | hp2 | a0003 | c0019 | t0003 | g0013 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01258 | hp1 | a0003 | c0004 | t0003 | g0047 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01258 | hp2 | a0001 | c0007 | t0006 | g0001 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01261 | hp1 | a0003 | c0004 | t0003 | g0019 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01346 | hp2 | a0003 | c0004 | t0003 | g0019 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01358 | hp1 | a0003 | c0004 | t0003 | g0144 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01358 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0157 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01433 | hp1 | a0001 | c0007 | t0001 | g0016 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01433 | hp2 | a0003 | c0004 | t0003 | g0165 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01496 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01496 | hp2 | a0004 | c0005 | t0001 | g0006 | AMR | CLM | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01515 | hp1 | a0012 | c0039 | t0005 | g0060 | EUR | IBS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01515 | hp2 | a0003 | c0004 | t0003 | g0019 | EUR | IBS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01516 | hp1 | a0003 | c0004 | t0003 | g0150 | EUR | IBS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01517 | hp1 | a0003 | c0004 | t0003 | g0019 | EUR | IBS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01884 | hp1 | a0008 | c0012 | t0001 | g0171 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01891 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01891 | hp2 | a0005 | c0008 | t0004 | g0008 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01934 | hp2 | a0001 | c0007 | t0001 | g0016 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01943 | hp1 | a0003 | c0004 | t0003 | g0142 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01943 | hp2 | a0001 | c0006 | t0001 | g0005 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01952 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01978 | hp1 | a0014 | c0021 | t0001 | g0005 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01981 | hp1 | a0001 | c0007 | t0001 | g0016 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01981 | hp2 | a0001 | c0022 | t0001 | g0054 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG01993 | hp2 | a0001 | c0006 | t0001 | g0005 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02004 | hp1 | a0002 | c0003 | t0002 | g0020 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02004 | hp2 | a0003 | c0004 | t0003 | g0046 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0138 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02055 | hp1 | a0001 | c0010 | t0001 | g0059 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02055 | hp2 | a0005 | c0008 | t0004 | g0008 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02071 | hp2 | a0003 | c0004 | t0003 | g0013 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02083 | hp1 | a0001 | c0018 | t0001 | g0163 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02132 | hp1 | a0015 | c0027 | t0001 | g0010 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02148 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02165 | hp1 | a0001 | c0018 | t0001 | g0156 | EAS | CDX | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02165 | hp2 | a0007 | c0026 | t0001 | g0010 | EAS | CDX | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02257 | hp1 | a0005 | c0008 | t0004 | g0179 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02257 | hp2 | a0003 | c0004 | t0003 | g0146 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02258 | hp1 | a0009 | c0011 | t0001 | g0030 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02280 | hp1 | a0008 | c0012 | t0001 | g0023 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02280 | hp2 | a0006 | c0009 | t0001 | g0034 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02293 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02300 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02300 | hp2 | a0003 | c0019 | t0003 | g0148 | AMR | PEL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02451 | hp1 | a0006 | c0009 | t0001 | g0176 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02451 | hp2 | a0006 | c0009 | t0001 | g0034 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02572 | hp1 | a0009 | c0011 | t0001 | g0031 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02602 | hp2 | a0001 | c0007 | t0001 | g0016 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02615 | hp1 | a0005 | c0008 | t0004 | g0008 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02630 | hp1 | a0016 | c0037 | t0002 | g0083 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02630 | hp2 | a0004 | c0005 | t0001 | g0006 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02647 | hp1 | a0008 | c0012 | t0001 | g0023 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02683 | hp2 | a0003 | c0004 | t0003 | g0012 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02717 | hp1 | a0005 | c0008 | t0004 | g0008 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02723 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02723 | hp2 | a0001 | c0038 | t0001 | g0172 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02735 | hp1 | a0001 | c0007 | t0001 | g0001 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02738 | hp1 | a0001 | c0007 | t0006 | g0001 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02809 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02818 | hp1 | a0003 | c0004 | t0002 | g0153 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02886 | hp2 | a0003 | c0004 | t0002 | g0149 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02895 | hp1 | a0009 | c0011 | t0001 | g0031 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02895 | hp2 | a0001 | c0017 | t0004 | g0051 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02896 | hp2 | a0017 | c0040 | t0007 | g0177 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02897 | hp1 | a0001 | c0017 | t0004 | g0051 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02922 | hp1 | a0004 | c0005 | t0011 | g0006 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02922 | hp2 | a0006 | c0009 | t0001 | g0094 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02965 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02970 | hp2 | a0005 | c0020 | t0004 | g0008 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03041 | hp2 | a0018 | c0032 | t0001 | g0169 | AFR | GWD | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03098 | hp1 | a0006 | c0009 | t0001 | g0109 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03130 | hp2 | a0019 | c0033 | t0001 | g0143 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03139 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03139 | hp2 | a0011 | c0013 | t0001 | g0050 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03195 | hp1 | a0011 | c0013 | t0001 | g0050 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0035 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03225 | hp1 | a0005 | c0008 | t0004 | g0052 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03225 | hp2 | a0003 | c0004 | t0002 | g0152 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03239 | hp1 | a0010 | c0015 | t0005 | g0055 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03239 | hp2 | a0001 | c0007 | t0006 | g0116 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03453 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03453 | hp2 | a0001 | c0010 | t0001 | g0058 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03486 | hp2 | a0004 | c0005 | t0001 | g0006 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03491 | hp1 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03491 | hp2 | a0013 | c0016 | t0001 | g0021 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0118 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03492 | hp2 | a0013 | c0016 | t0001 | g0021 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03516 | hp1 | a0005 | c0008 | t0004 | g0008 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03516 | hp2 | a0006 | c0009 | t0001 | g0175 | AFR | ESN | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03579 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03579 | hp2 | a0002 | c0003 | t0002 | g0164 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0020 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03704 | hp2 | a0003 | c0004 | t0002 | g0020 | SAS | PJL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03831 | hp2 | a0003 | c0004 | t0002 | g0020 | SAS | BEB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03834 | hp1 | a0001 | c0035 | t0001 | g0081 | SAS | BEB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | STU | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | BEB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18522 | hp1 | a0002 | c0003 | t0002 | g0108 | AFR | YRI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | CHB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18906 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | YRI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18939 | hp1 | a0003 | c0004 | t0003 | g0147 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18940 | hp1 | a0002 | c0003 | t0002 | g0166 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18942 | hp1 | a0002 | c0003 | t0002 | g0160 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18952 | hp1 | a0003 | c0004 | t0003 | g0037 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18957 | hp1 | a0020 | c0029 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18959 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18960 | hp2 | a0002 | c0003 | t0010 | g0049 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18962 | hp1 | a0002 | c0003 | t0002 | g0159 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18964 | hp2 | a0001 | c0024 | t0001 | g0126 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18973 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18977 | hp1 | a0003 | c0004 | t0003 | g0117 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18988 | hp2 | a0002 | c0003 | t0002 | g0049 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18991 | hp1 | a0002 | c0003 | t0002 | g0162 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18994 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA18999 | hp2 | a0003 | c0004 | t0003 | g0037 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19002 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19004 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19005 | hp2 | a0021 | c0034 | t0001 | g0071 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19006 | hp1 | a0022 | c0028 | t0001 | g0015 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19009 | hp1 | a0001 | c0002 | t0008 | g0064 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19009 | hp2 | a0002 | c0003 | t0002 | g0161 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19030 | hp1 | a0023 | c0025 | t0001 | g0029 | AFR | LWK | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19030 | hp2 | a0002 | c0003 | t0002 | g0155 | AFR | LWK | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19043 | hp1 | a0004 | c0005 | t0001 | g0111 | AFR | LWK | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19043 | hp2 | a0005 | c0020 | t0004 | g0008 | AFR | LWK | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19080 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19083 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19240 | hp1 | a0002 | c0003 | t0002 | g0158 | AFR | YRI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA19240 | hp2 | a0001 | c0010 | t0001 | g0057 | AFR | YRI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20129 | hp1 | a0005 | c0008 | t0004 | g0052 | AFR | ASW | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20129 | hp2 | a0003 | c0004 | t0003 | g0115 | AFR | ASW | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20805 | hp1 | a0002 | c0003 | t0003 | g0013 | EUR | TSI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20805 | hp2 | a0003 | c0004 | t0003 | g0047 | EUR | TSI | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | GIH | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02109 | hp1 | a0001 | c0023 | t0001 | g0077 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02109 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02486 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02486 | hp2 | a0011 | c0013 | t0001 | g0170 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02559 | hp1 | a0007 | c0014 | t0001 | g0025 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG02559 | hp2 | a0007 | c0014 | t0001 | g0151 | AFR | ACB | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03471 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG03471 | hp2 | a0008 | c0012 | t0001 | g0023 | AFR | MSL | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | USA | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
HG06807 | hp2 | a0009 | c0011 | t0001 | g0030 | AFR | USA | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20300 | hp1 | a0004 | c0005 | t0001 | g0035 | AFR | USA | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA20300 | hp2 | a0005 | c0008 | t0004 | g0008 | AFR | USA | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA21309 | hp1 | a0024 | c0030 | t0001 | g0110 | AFR | LWK | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
NA21309 | hp2 | a0003 | c0004 | t0003 | g0141 | AFR | LWK | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
homoSapiens | chm13v2 | a0002 | c0003 | t0003 | g0154 | REF | REF | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0087 | REF | REF | INCENP_chr11_62119011_62158169 | INCENP | chr11 | 62119011 | 62158169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:62128166 | G | T | 2 | a0005 a0017 |
12 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.5G>T | p.Gly2Val | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/19 | 169/4114 | 5/2757 | 2/918 | chr11 | 62128166 | |||
chr11:62129825 | C | T | 1 | a0021 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.298C>T | p.Arg100Cys | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 462/4114 | 298/2757 | 100/918 | chr11 | 62129825 | |||
chr11:62129826 | G | A | 1 | a0004 | 13 | HG01496.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
missense_variant | MODERATE | c.299G>A | p.Arg100His | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 463/4114 | 299/2757 | 100/918 | chr11 | 62129826 | |||
chr11:62129937 | C | T | 3 | a0006 a0018 a0019 |
8 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
missense_variant | MODERATE | c.410C>T | p.Ala137Val | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 574/4114 | 410/2757 | 137/918 | chr11 | 62129937 | |||
chr11:62129996 | G | A | 1 | a0011 | 3 | HG02486.hp2 HG03139.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.469G>A | p.Glu157Lys | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 633/4114 | 469/2757 | 157/918 | chr11 | 62129996 | |||
chr11:62130120 | C | T | 1 | a0019 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.593C>T | p.Pro198Leu | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 757/4114 | 593/2757 | 198/918 | chr11 | 62130120 | |||
chr11:62130281 | C | T | 1 | a0012 | 2 | HG01109.hp1 HG01515.hp1 |
missense_variant | MODERATE | c.754C>T | p.Arg252Trp | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 918/4114 | 754/2757 | 252/918 | chr11 | 62130281 | |||
chr11:62130327 | G | A | 1 | a0016 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.800G>A | p.Arg267Gln | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 964/4114 | 800/2757 | 267/918 | chr11 | 62130327 | |||
chr11:62130437 | C | T | 1 | a0024 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.910C>T | p.Arg304Trp | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 1074/4114 | 910/2757 | 304/918 | chr11 | 62130437 | |||
chr11:62138744 | G | A | 1 | a0009 | 4 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.1147G>A | p.Glu383Lys | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 6/19 | 1311/4114 | 1147/2757 | 383/918 | chr11 | 62138744 | |||
chr11:62140968 | T | C | 3 | a0002 a0007 a0016 |
49 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(46): Show |
missense_variant | MODERATE | c.1517T>C | p.Met506Thr | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/19 | 1681/4114 | 1517/2757 | 506/918 | chr11 | 62140968 | |||
chr11:62145672 | C | T | 1 | a0008 | 4 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
missense_variant | MODERATE | c.1880C>T | p.Ala627Val | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/19 | 2044/4114 | 1880/2757 | 627/918 | chr11 | 62145672 | |||
chr11:62145724 | G | T | 3 | a0002 a0003 a0016 |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
missense_variant | MODERATE | c.1932G>T | p.Glu644Asp | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/19 | 2096/4114 | 1932/2757 | 644/918 | chr11 | 62145724 | |||
chr11:62146758 | A | AGCGGGAG others(8): Show |
1 | a0004 | 13 | HG01496.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
disruptive_inframe_insertion | MODERATE | c.2079_2093dupGGAGCA others(9): Show |
p.Arg698_Glu699insGl others(13): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2258/4114 | 2094/2757 | 698/918 | INFO_REALIGN_3_PRIME | chr11 | 62146758 | ||
chr11:62146762 | GGAGCAGG others(23): Show |
G | 1 | a0013 | 2 | HG03491.hp2 HG03492.hp2 |
disruptive_inframe_deletion | MODERATE | c.2079_2108delGGAGCA others(24): Show |
p.Glu694_Arg703del | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2243/4114 | 2079/2757 | 693/918 | INFO_REALIGN_3_PRIME | chr11 | 62146762 | ||
chr11:62146777 | G | GGAGCAGG others(8): Show |
1 | a0001 | 2 | HG02273.hp2 NA18983.hp2 |
disruptive_inframe_insertion | MODERATE | c.2089_2090insAGCGCG others(9): Show |
p.Glu696_Arg697insGl others(13): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2254/4114 | 2090/2757 | 697/918 | INFO_REALIGN_3_PRIME | chr11 | 62146777 | ||
chr11:62146777 | G | GGAGCAGG others(8): Show |
2 | a0006 a0009 |
5 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.2109_2123dupCGAGCA others(9): Show |
p.Arg708_Glu709insGl others(13): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2288/4114 | 2124/2757 | 708/918 | INFO_REALIGN_3_PRIME | chr11 | 62146777 | ||
chr11:62146777 | GGAGCAGG others(8): Show |
G | 1 | a0001 | 2 | HG00099.hp2 HG03098.hp2 |
disruptive_inframe_deletion | MODERATE | c.2109_2123delCGAGCA others(9): Show |
p.Glu704_Arg708del | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2273/4114 | 2109/2757 | 703/918 | INFO_REALIGN_3_PRIME | chr11 | 62146777 | ||
chr11:62146777 | GGAGCAGG others(23): Show |
G | 1 | a0006 | 1 | HG03098.hp1 | disruptive_inframe_deletion | MODERATE | c.2094_2123delCGAGCA others(24): Show |
p.Glu699_Arg708del | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2258/4114 | 2094/2757 | 698/918 | INFO_REALIGN_3_PRIME | chr11 | 62146777 | ||
chr11:62146788 | G | A | 5 | a0001 a0007 a0015 others(2): Show |
81 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(78): Show |
missense_variant | MODERATE | c.2090G>A | p.Arg697Gln | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2254/4114 | 2090/2757 | 697/918 | chr11 | 62146788 | |||
chr11:62146807 | C | CGAGCAGG others(8): Show |
1 | a0017 | 1 | HG02896.hp2 | disruptive_inframe_insertion | MODERATE | c.2124_2138dupGGAGCA others(9): Show |
p.Arg713_Glu714insGl others(13): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2303/4114 | 2139/2757 | 713/918 | INFO_REALIGN_3_PRIME | chr11 | 62146807 | ||
chr11:62148498 | G | A | 1 | a0015 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.2227G>A | p.Ala743Thr | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 16/19 | 2391/4114 | 2227/2757 | 743/918 | chr11 | 62148498 | |||
chr11:62148752 | G | A | 1 | a0022 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2297G>A | p.Arg766His | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/19 | 2461/4114 | 2297/2757 | 766/918 | chr11 | 62148752 | |||
chr11:62150080 | G | C | 1 | a0010 | 3 | HG01168.hp1 HG01169.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.2415G>C | p.Gln805His | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/19 | 2579/4114 | 2415/2757 | 805/918 | chr11 | 62150080 | |||
chr11:62150112 | A | C | 1 | a0020 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.2447A>C | p.Lys816Thr | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/19 | 2611/4114 | 2447/2757 | 816/918 | chr11 | 62150112 | |||
chr11:62150114 | A | G | 1 | a0014 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2449A>G | p.Ile817Val | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/19 | 2613/4114 | 2449/2757 | 817/918 | chr11 | 62150114 | |||
chr11:62151912 | A | G | 1 | a0018 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.2693A>G | p.Asn898Ser | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 2857/4114 | 2693/2757 | 898/918 | chr11 | 62151912 | |||
chr11:62151953 | G | A | 1 | a0023 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2734G>A | p.Ala912Thr | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 2898/4114 | 2734/2757 | 912/918 | chr11 | 62151953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:62128269 | A | G | 13 | a0001c0010 a0001c0018 a0001c0036 others(10): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
synonymous_variant | LOW | c.108A>G | p.Glu36Glu | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/19 | 272/4114 | 108/2757 | 36/918 | chr11 | 62128269 | |||
chr11:62128290 | C | T | 1 | a0001c0035 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.129C>T | p.Arg43Arg | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/19 | 293/4114 | 129/2757 | 43/918 | chr11 | 62128290 | |||
chr11:62129887 | C | T | 12 | a0001c0010 a0001c0038 a0002c0003 others(9): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
synonymous_variant | LOW | c.360C>T | p.Val120Val | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 524/4114 | 360/2757 | 120/918 | chr11 | 62129887 | |||
chr11:62129932 | C | T | 1 | a0003c0019 | 2 | HG01255.hp2 HG02300.hp2 |
synonymous_variant | LOW | c.405C>T | p.Thr135Thr | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/19 | 569/4114 | 405/2757 | 135/918 | chr11 | 62129932 | |||
chr11:62138902 | T | C | 31 | a0001c0001 a0001c0006 a0001c0007 others(28): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
synonymous_variant | LOW | c.1188T>C | p.Asn396Asn | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/19 | 1352/4114 | 1188/2757 | 396/918 | chr11 | 62138902 | |||
chr11:62140244 | G | A | 3 | a0001c0006 a0001c0022 a0014c0021 |
12 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(9): Show |
synonymous_variant | LOW | c.1302G>A | p.Thr434Thr | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/19 | 1466/4114 | 1302/2757 | 434/918 | chr11 | 62140244 | |||
chr11:62146810 | G | A | 4 | a0001c0010 a0001c0023 a0010c0015 others(1): Show |
11 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(8): Show |
synonymous_variant | LOW | c.2112G>A | p.Glu704Glu | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2276/4114 | 2112/2757 | 704/918 | chr11 | 62146810 | |||
chr11:62146897 | C | T | 2 | a0001c0007 a0001c0022 |
11 | HG01070.hp1 HG01071.hp2 HG01258.hp2 others(8): Show |
synonymous_variant | LOW | c.2199C>T | p.Ala733Ala | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/19 | 2363/4114 | 2199/2757 | 733/918 | chr11 | 62146897 | |||
chr11:62148840 | C | T | 4 | a0001c0017 a0005c0008 a0005c0020 others(1): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
synonymous_variant | LOW | c.2385C>T | p.Asp795Asp | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/19 | 2549/4114 | 2385/2757 | 795/918 | chr11 | 62148840 | |||
chr11:62151919 | G | A | 1 | a0001c0024 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.2700G>A | p.Pro900Pro | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 2864/4114 | 2700/2757 | 900/918 | chr11 | 62151919 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:62152006 | G | A | 4 | a0001c0017t0004 a0005c0008t0004 a0005c0020t0004 others(1): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*30G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 30 | chr11 | 62152006 | ||||||
chr11:62152043 | C | G | 3 | a0002c0003t0003 a0003c0004t0003 a0003c0019t0003 |
30 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*67C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 67 | chr11 | 62152043 | ||||||
chr11:62152089 | C | T | 1 | a0004c0005t0011 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 113 | chr11 | 62152089 | ||||||
chr11:62152097 | G | C | 3 | a0001c0010t0005 a0010c0015t0005 a0012c0039t0005 |
7 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*121G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 121 | chr11 | 62152097 | ||||||
chr11:62152221 | C | T | 4 | a0002c0003t0002 a0002c0003t0010 a0003c0004t0002 others(1): Show |
48 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*245C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 245 | chr11 | 62152221 | ||||||
chr11:62152501 | C | T | 1 | a0012c0031t0009 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*525C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 525 | chr11 | 62152501 | ||||||
chr11:62152524 | C | T | 1 | a0001c0002t0008 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*548C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 548 | chr11 | 62152524 | ||||||
chr11:62152711 | G | A | 4 | a0001c0017t0004 a0005c0008t0004 a0005c0020t0004 others(1): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 735 | chr11 | 62152711 | ||||||
chr11:62152731 | C | T | 1 | a0017c0040t0007 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*755C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 755 | chr11 | 62152731 | ||||||
chr11:62152753 | G | A | 1 | a0001c0007t0006 | 3 | HG01258.hp2 HG02738.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*777G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 777 | chr11 | 62152753 | ||||||
chr11:62152928 | T | C | 1 | a0012c0031t0009 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 952 | chr11 | 62152928 | ||||||
chr11:62152968 | G | A | 1 | a0002c0003t0010 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 19/19 | 992 | chr11 | 62152968 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:62124174 | G | A | 13 | a0001c0001t0001g0053 a0001c0006t0001g0005 a0001c0010t0001g0057 others(10): Show |
25 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12+11G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124174 | |||||||
chr11:62124300 | C | T | 6 | a0005c0008t0004g0008 a0005c0008t0004g0052 a0005c0008t0004g0179 others(3): Show |
13 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+137C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124300 | |||||||
chr11:62124425 | C | CTTGTT | 65 | a0001c0001t0001g0053 a0001c0001t0001g0145 a0001c0001t0001g0167 others(62): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+266_-12+267ins others(5): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62124425 | ||||||
chr11:62124459 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-12+296C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124459 | |||||||
chr11:62124577 | C | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0140 |
3 | HG02145.hp1 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-12+414C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124577 | |||||||
chr11:62124623 | G | A | 2 | a0001c0001t0001g0021 a0013c0016t0001g0021 |
3 | HG02738.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+460G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124623 | |||||||
chr11:62124638 | G | C | 20 | a0001c0001t0001g0063 a0001c0002t0001g0002 a0001c0002t0001g0010 others(17): Show |
41 | HG00423.hp2 HG00544.hp2 HG02040.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12+475G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124638 | |||||||
chr11:62124731 | G | A | 1 | a0003c0004t0003g0141 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-12+568G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124731 | |||||||
chr11:62124749 | G | C | 39 | a0001c0001t0001g0145 a0001c0018t0001g0156 a0001c0018t0001g0163 others(36): Show |
75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-12+586G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124749 | |||||||
chr11:62124765 | A | G | 65 | a0001c0001t0001g0053 a0001c0001t0001g0145 a0001c0001t0001g0167 others(62): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+602A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124765 | |||||||
chr11:62124825 | C | A | 1 | a0001c0002t0001g0014 | 4 | HG01934.hp1 HG02273.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+662C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124825 | |||||||
chr11:62124915 | A | G | 65 | a0001c0001t0001g0053 a0001c0001t0001g0145 a0001c0001t0001g0167 others(62): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+752A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62124915 | |||||||
chr11:62125195 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(45): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-12+1032C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125195 | |||||||
chr11:62125246 | C | G | 66 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(63): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12+1083C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125246 | |||||||
chr11:62125586 | T | C | 66 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(63): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12+1423T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125586 | |||||||
chr11:62125719 | G | A | 1 | a0003c0004t0003g0142 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-12+1556G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125719 | |||||||
chr11:62125744 | T | G | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+1581T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125744 | |||||||
chr11:62125772 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12+1609G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125772 | |||||||
chr11:62125787 | G | C | 1 | a0017c0040t0007g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12+1624G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125787 | |||||||
chr11:62125797 | C | T | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-12+1634C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125797 | |||||||
chr11:62125884 | G | T | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-12+1721G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62125884 | |||||||
chr11:62126067 | G | A | 6 | a0003c0004t0003g0012 a0003c0004t0003g0046 a0003c0004t0003g0141 others(3): Show |
11 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+1904G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126067 | |||||||
chr11:62126191 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(121): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-11-1960T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126191 | |||||||
chr11:62126200 | G | GT | 5 | a0001c0006t0001g0005 a0001c0022t0001g0054 a0006c0009t0001g0034 others(2): Show |
15 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-1938dupT | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62126200 | ||||||
chr11:62126200 | G | GTTTTT | 18 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(15): Show |
31 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11-1942_-11-1938d others(7): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62126200 | ||||||
chr11:62126200 | GT | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(50): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-11-1938delT | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62126200 | ||||||
chr11:62126202 | T | TTTTTTG | 42 | a0001c0001t0001g0145 a0001c0018t0001g0156 a0001c0018t0001g0163 others(39): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.-11-1944_-11-1943i others(8): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62126202 | ||||||
chr11:62126208 | T | TTTTTTC | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-1938_-11-1937i others(8): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62126208 | ||||||
chr11:62126218 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(121): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-11-1933T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126218 | |||||||
chr11:62126222 | G | A | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-1929G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126222 | |||||||
chr11:62126234 | T | C | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1917T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126234 | |||||||
chr11:62126249 | GC | G | 5 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(2): Show |
14 | HG01496.hp2 HG02486.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11-1901delC | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126249 | |||||||
chr11:62126269 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(45): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-11-1882C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126269 | |||||||
chr11:62126341 | G | A | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1810G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126341 | |||||||
chr11:62126357 | A | G | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1794A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126357 | |||||||
chr11:62126396 | C | T | 1 | a0005c0008t0004g0052 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-11-1755C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126396 | |||||||
chr11:62126438 | T | C | 73 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(70): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-11-1713T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126438 | |||||||
chr11:62126466 | G | C | 5 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(2): Show |
14 | HG01496.hp2 HG02486.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11-1685G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126466 | |||||||
chr11:62126492 | G | A | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-11-1659G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126492 | |||||||
chr11:62126496 | A | G | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1655A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126496 | |||||||
chr11:62126500 | C | T | 18 | a0001c0018t0001g0156 a0001c0018t0001g0163 a0002c0003t0002g0003 others(15): Show |
43 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11-1651C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126500 | |||||||
chr11:62126558 | A | G | 21 | a0001c0001t0001g0145 a0002c0003t0003g0013 a0003c0004t0002g0149 others(18): Show |
32 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11-1593A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126558 | |||||||
chr11:62126561 | T | C | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1590T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126561 | |||||||
chr11:62126708 | A | T | 1 | a0002c0003t0002g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-11-1443A>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126708 | |||||||
chr11:62126772 | C | A | 5 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(2): Show |
14 | HG01496.hp2 HG02486.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11-1379C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126772 | |||||||
chr11:62126808 | T | C | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1343T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62126808 | |||||||
chr11:62126822 | T | TA | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-1328dupA | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62126822 | ||||||
chr11:62127010 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(122): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.-11-1141A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127010 | |||||||
chr11:62127019 | A | G | 1 | a0012c0039t0005g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-11-1132A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127019 | |||||||
chr11:62127042 | TG | T | 9 | a0001c0018t0001g0163 a0002c0003t0002g0007 a0002c0003t0002g0049 others(6): Show |
16 | HG00597.hp1 HG02083.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-1108delG | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127042 | |||||||
chr11:62127043 | G | GT | 50 | a0001c0001t0001g0079 a0001c0001t0001g0145 a0001c0001t0001g0167 others(47): Show |
72 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-1095dupT | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62127043 | ||||||
chr11:62127043 | G | GTT | 7 | a0003c0004t0003g0012 a0004c0005t0001g0006 a0004c0005t0001g0035 others(4): Show |
16 | HG01168.hp2 HG01496.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-1096_-11-1095d others(4): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62127043 | ||||||
chr11:62127043 | G | T | 10 | a0001c0018t0001g0156 a0002c0003t0002g0003 a0002c0003t0002g0020 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-1108G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127043 | |||||||
chr11:62127043 | GT | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(49): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-11-1095delT | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62127043 | ||||||
chr11:62127067 | C | T | 1 | a0001c0002t0001g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-11-1084C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127067 | |||||||
chr11:62127068 | G | A | 1 | a0001c0035t0001g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11-1083G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127068 | |||||||
chr11:62127092 | A | G | 1 | a0017c0040t0007g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-11-1059A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127092 | |||||||
chr11:62127138 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-11-1013G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127138 | |||||||
chr11:62127197 | C | T | 66 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(63): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11-954C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127197 | |||||||
chr11:62127198 | A | G | 71 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-11-953A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127198 | |||||||
chr11:62127326 | A | G | 69 | a0001c0001t0001g0079 a0001c0001t0001g0145 a0001c0001t0001g0167 others(66): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-11-825A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127326 | |||||||
chr11:62127329 | C | T | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-822C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127329 | |||||||
chr11:62127400 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11-751T>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127400 | |||||||
chr11:62127402 | G | T | 38 | a0001c0001t0001g0063 a0001c0002t0001g0002 a0001c0002t0001g0004 others(35): Show |
84 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11-749G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127402 | |||||||
chr11:62127419 | A | G | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-732A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127419 | |||||||
chr11:62127516 | G | T | 2 | a0001c0010t0005g0026 a0012c0039t0005g0060 |
3 | HG01069.hp1 HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-11-635G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127516 | |||||||
chr11:62127521 | T | G | 67 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0001t0001g0168 others(64): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-11-630T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127521 | |||||||
chr11:62127628 | T | C | 21 | a0001c0001t0001g0036 a0001c0001t0001g0114 a0001c0001t0001g0145 others(18): Show |
33 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-523T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127628 | |||||||
chr11:62127697 | C | T | 63 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(60): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-11-454C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127697 | |||||||
chr11:62127971 | TA | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(122): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-11-179delA | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127971 | |||||||
chr11:62127972 | A | G | 1 | a0001c0007t0001g0016 | 4 | HG01433.hp1 HG01934.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-179A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62127972 | |||||||
chr11:62127972 | AG | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0085 a0001c0001t0001g0086 others(10): Show |
18 | HG01884.hp1 HG02280.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11-175delG | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 62127972 | ||||||
chr11:62128004 | G | A | 25 | a0001c0001t0001g0082 a0001c0010t0005g0056 a0001c0018t0001g0156 others(22): Show |
50 | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-11-147G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62128004 | |||||||
chr11:62128069 | A | G | 64 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(61): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-11-82A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 1/18 | chr11 | 62128069 | |||||||
chr11:62128332 | C | T | 4 | a0001c0017t0004g0051 a0001c0023t0001g0077 a0008c0012t0001g0023 others(1): Show |
7 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+31C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/18 | chr11 | 62128332 | |||||||
chr11:62128413 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.140+112G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/18 | chr11 | 62128413 | |||||||
chr11:62128677 | G | A | 1 | a0001c0002t0001g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.141-93G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/18 | chr11 | 62128677 | |||||||
chr11:62128743 | G | A | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.141-27G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/18 | chr11 | 62128743 | |||||||
chr11:62128757 | T | A | 1 | a0001c0002t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.141-13T>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 2/18 | chr11 | 62128757 | |||||||
chr11:62129117 | T | G | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.254+234T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129117 | |||||||
chr11:62129156 | G | A | 4 | a0001c0017t0004g0051 a0001c0023t0001g0077 a0008c0012t0001g0023 others(1): Show |
7 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.254+273G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129156 | |||||||
chr11:62129181 | A | G | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.254+298A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129181 | |||||||
chr11:62129204 | C | T | 4 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(1): Show |
5 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+321C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129204 | |||||||
chr11:62129239 | C | T | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.254+356C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129239 | |||||||
chr11:62129247 | C | T | 2 | a0011c0013t0001g0050 a0011c0013t0001g0170 |
3 | HG02486.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.254+364C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129247 | |||||||
chr11:62129478 | G | A | 1 | a0001c0023t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.255-304G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129478 | |||||||
chr11:62129599 | T | C | 1 | a0001c0002t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.255-183T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129599 | |||||||
chr11:62129601 | C | T | 3 | a0001c0010t0005g0056 a0010c0015t0005g0024 a0010c0015t0005g0055 |
4 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-181C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129601 | |||||||
chr11:62129602 | G | A | 1 | a0001c0038t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.255-180G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129602 | |||||||
chr11:62129725 | C | T | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.255-57C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129725 | |||||||
chr11:62129744 | G | T | 1 | a0018c0032t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.255-38G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 3/18 | chr11 | 62129744 | |||||||
chr11:62130593 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.1063+3G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130593 | |||||||
chr11:62130695 | A | G | 2 | a0004c0005t0001g0035 a0004c0005t0001g0111 |
3 | HG03209.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1063+105A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130695 | |||||||
chr11:62130702 | T | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0100 |
3 | HG00323.hp2 HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1063+112T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130702 | |||||||
chr11:62130720 | G | A | 48 | a0001c0038t0001g0172 a0002c0003t0002g0003 a0002c0003t0002g0007 others(45): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1063+130G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130720 | |||||||
chr11:62130853 | A | G | 7 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1063+263A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130853 | |||||||
chr11:62130911 | T | C | 1 | a0003c0004t0003g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1063+321T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130911 | |||||||
chr11:62130979 | G | A | 1 | a0001c0001t0001g0039 | 2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1063+389G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62130979 | |||||||
chr11:62131025 | C | T | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1063+435C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131025 | |||||||
chr11:62131072 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1063+482G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131072 | |||||||
chr11:62131089 | G | A | 48 | a0001c0038t0001g0172 a0002c0003t0002g0003 a0002c0003t0002g0007 others(45): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1063+499G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131089 | |||||||
chr11:62131189 | G | A | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(3): Show |
7 | HG02145.hp2 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+599G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131189 | |||||||
chr11:62131284 | T | G | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+694T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131284 | |||||||
chr11:62131387 | T | C | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+797T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131387 | |||||||
chr11:62131406 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1063+816T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131406 | |||||||
chr11:62131510 | G | A | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1063+920G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131510 | |||||||
chr11:62131569 | G | A | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1063+979G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131569 | |||||||
chr11:62131573 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1063+983G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131573 | |||||||
chr11:62131606 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(41): Show |
87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1063+1016G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131606 | |||||||
chr11:62131718 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1063+1128G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131718 | |||||||
chr11:62131739 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0084 |
3 | HG02809.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1063+1149G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131739 | |||||||
chr11:62131743 | A | G | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+1153A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131743 | |||||||
chr11:62131812 | C | T | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1063+1222C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131812 | |||||||
chr11:62131862 | C | T | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+1272C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131862 | |||||||
chr11:62131906 | C | T | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1063+1316C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131906 | |||||||
chr11:62131926 | C | T | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+1336C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62131926 | |||||||
chr11:62132040 | T | C | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+1450T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132040 | |||||||
chr11:62132074 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1063+1484C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132074 | |||||||
chr11:62132359 | G | C | 1 | a0001c0010t0001g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063+1769G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132359 | |||||||
chr11:62132451 | A | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG02451.hp1 HG02602.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063+1861A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132451 | |||||||
chr11:62132454 | C | G | 1 | a0001c0002t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1063+1864C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132454 | |||||||
chr11:62132523 | G | T | 1 | a0001c0002t0001g0137 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1063+1933G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132523 | |||||||
chr11:62132631 | G | A | 1 | a0007c0014t0001g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1063+2041G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62132631 | |||||||
chr11:62133107 | G | A | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+2517G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133107 | |||||||
chr11:62133231 | GGAAATTA others(197): Show |
G | 1 | a0001c0001t0001g0018 | 4 | HG00423.hp1 HG02135.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+2643_1063+284 others(4): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62133231 | ||||||
chr11:62133268 | G | A | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+2678G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133268 | |||||||
chr11:62133281 | A | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(3): Show |
7 | HG02145.hp2 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+2691A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133281 | |||||||
chr11:62133337 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1063+2747G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133337 | |||||||
chr11:62133349 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0084 |
3 | HG02809.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1063+2759G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133349 | |||||||
chr11:62133351 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0084 |
3 | HG02809.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1063+2761C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133351 | |||||||
chr11:62133434 | G | C | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+2844G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133434 | |||||||
chr11:62133515 | C | T | 22 | a0002c0003t0003g0013 a0003c0004t0002g0149 a0003c0004t0002g0152 others(19): Show |
34 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1063+2925C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133515 | |||||||
chr11:62133542 | C | G | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+2952C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133542 | |||||||
chr11:62133612 | T | G | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+3022T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133612 | |||||||
chr11:62133613 | C | T | 1 | a0003c0004t0003g0046 | 2 | HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1063+3023C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133613 | |||||||
chr11:62133660 | G | A | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1063+3070G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133660 | |||||||
chr11:62133883 | C | T | 57 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(54): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1063+3293C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62133883 | |||||||
chr11:62134012 | A | G | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1063+3422A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134012 | |||||||
chr11:62134106 | G | A | 2 | a0003c0004t0002g0152 a0003c0004t0002g0153 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1063+3516G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134106 | |||||||
chr11:62134359 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1064-3473G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134359 | |||||||
chr11:62134383 | A | AGCCTAGG others(1): Show |
68 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(65): Show |
116 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1064-3448_1064-344 others(12): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62134383 | ||||||
chr11:62134402 | T | TA | 17 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0095 others(14): Show |
21 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1064-3412dupA | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62134402 | ||||||
chr11:62134402 | T | TAA | 13 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0039 others(10): Show |
22 | HG00597.hp2 HG01074.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1064-3413_1064-341 others(6): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62134402 | ||||||
chr11:62134402 | T | TAAA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(37): Show |
74 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1064-3414_1064-341 others(7): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62134402 | ||||||
chr11:62134402 | T | TAAAA | 6 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0139 others(3): Show |
8 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064-3415_1064-341 others(8): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62134402 | ||||||
chr11:62134402 | TA | T | 11 | a0001c0001t0001g0097 a0001c0002t0001g0074 a0004c0005t0001g0006 others(8): Show |
27 | HG01496.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1064-3412delA | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62134402 | ||||||
chr11:62134417 | A | C | 47 | a0001c0038t0001g0172 a0002c0003t0002g0003 a0002c0003t0002g0007 others(44): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1064-3415A>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134417 | |||||||
chr11:62134478 | G | A | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1064-3354G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134478 | |||||||
chr11:62134505 | A | C | 1 | a0003c0004t0003g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1064-3327A>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134505 | |||||||
chr11:62134608 | C | T | 2 | a0001c0001t0001g0079 a0001c0036t0001g0080 |
2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1064-3224C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134608 | |||||||
chr11:62134654 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(65): Show |
116 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1064-3178C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134654 | |||||||
chr11:62134977 | G | A | 7 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064-2855G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62134977 | |||||||
chr11:62135034 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(115): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1064-2798C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135034 | |||||||
chr11:62135043 | T | C | 1 | a0001c0023t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1064-2789T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135043 | |||||||
chr11:62135236 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1064-2596C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135236 | |||||||
chr11:62135349 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0132 others(1): Show |
6 | NA18948.hp1 NA18981.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1064-2483C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135349 | |||||||
chr11:62135412 | G | A | 1 | a0003c0004t0003g0147 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1064-2420G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135412 | |||||||
chr11:62135544 | G | A | 5 | a0005c0008t0004g0008 a0005c0008t0004g0052 a0005c0008t0004g0179 others(2): Show |
12 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064-2288G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135544 | |||||||
chr11:62135614 | C | T | 1 | a0002c0003t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1064-2218C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135614 | |||||||
chr11:62135628 | A | G | 6 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(3): Show |
7 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1064-2204A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135628 | |||||||
chr11:62135903 | G | A | 4 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(1): Show |
5 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-1929G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135903 | |||||||
chr11:62135934 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(58): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1064-1898C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135934 | |||||||
chr11:62135971 | G | A | 2 | a0001c0001t0001g0029 a0023c0025t0001g0029 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1064-1861G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135971 | |||||||
chr11:62135992 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(58): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1064-1840C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62135992 | |||||||
chr11:62136087 | G | A | 3 | a0001c0001t0001g0079 a0001c0036t0001g0080 a0006c0009t0001g0094 |
3 | HG00642.hp2 HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1064-1745G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136087 | |||||||
chr11:62136215 | C | T | 1 | a0002c0003t0002g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1064-1617C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136215 | |||||||
chr11:62136275 | A | T | 42 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(39): Show |
88 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1064-1557A>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136275 | |||||||
chr11:62136338 | C | G | 47 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(44): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1064-1494C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136338 | |||||||
chr11:62136433 | G | A | 9 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064-1399G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136433 | |||||||
chr11:62136500 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(56): Show |
104 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1064-1332C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136500 | |||||||
chr11:62136637 | C | A | 1 | a0001c0002t0001g0065 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1064-1195C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136637 | |||||||
chr11:62136642 | C | A | 2 | a0002c0003t0002g0155 a0002c0003t0002g0158 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1064-1190C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136642 | |||||||
chr11:62136758 | G | A | 1 | a0001c0023t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1064-1074G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136758 | |||||||
chr11:62136911 | T | C | 1 | a0001c0002t0001g0066 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1064-921T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62136911 | |||||||
chr11:62137031 | TCAGGTCC others(3): Show |
T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1064-798_1064-789d others(12): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 62137031 | ||||||
chr11:62137032 | C | T | 1 | a0002c0003t0002g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1064-800C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137032 | |||||||
chr11:62137079 | C | T | 6 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(3): Show |
7 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1064-753C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137079 | |||||||
chr11:62137085 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0114 |
3 | HG01255.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1064-747G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137085 | |||||||
chr11:62137217 | C | T | 1 | a0004c0005t0001g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1064-615C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137217 | |||||||
chr11:62137218 | G | A | 1 | a0001c0002t0001g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1064-614G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137218 | |||||||
chr11:62137262 | C | T | 1 | a0001c0023t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1064-570C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137262 | |||||||
chr11:62137283 | A | G | 3 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 |
4 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-549A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137283 | |||||||
chr11:62137298 | G | A | 1 | a0003c0004t0002g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1064-534G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137298 | |||||||
chr11:62137560 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1064-272G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137560 | |||||||
chr11:62137587 | C | T | 1 | a0001c0002t0001g0073 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1064-245C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137587 | |||||||
chr11:62137611 | G | T | 1 | a0001c0038t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1064-221G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137611 | |||||||
chr11:62137725 | T | C | 1 | a0006c0009t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1064-107T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 4/18 | chr11 | 62137725 | |||||||
chr11:62137997 | A | G | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1115+114A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 5/18 | chr11 | 62137997 | |||||||
chr11:62138122 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(48): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1115+239C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 5/18 | chr11 | 62138122 | |||||||
chr11:62138187 | G | T | 1 | a0003c0004t0003g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1115+304G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 5/18 | chr11 | 62138187 | |||||||
chr11:62138383 | A | G | 2 | a0011c0013t0001g0050 a0011c0013t0001g0170 |
3 | HG02486.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1116-330A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 5/18 | chr11 | 62138383 | |||||||
chr11:62138440 | C | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0072 |
7 | NA18947.hp2 NA18968.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116-273C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 5/18 | chr11 | 62138440 | |||||||
chr11:62138513 | G | A | 7 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(4): Show |
18 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1116-200G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 5/18 | chr11 | 62138513 | |||||||
chr11:62138816 | C | T | 1 | a0016c0037t0002g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1173+46C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 6/18 | chr11 | 62138816 | |||||||
chr11:62138827 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(120): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1173+57A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 6/18 | chr11 | 62138827 | |||||||
chr11:62138882 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA19089.hp1 | splice_region_variant&intron_variant | LOW | c.1174-6C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 6/18 | chr11 | 62138882 | |||||||
chr11:62139021 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1291+16C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139021 | |||||||
chr11:62139038 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1291+33C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139038 | |||||||
chr11:62139066 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(41): Show |
87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1291+61G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139066 | |||||||
chr11:62139182 | C | T | 1 | a0006c0009t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1291+177C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139182 | |||||||
chr11:62139370 | C | T | 8 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291+365C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139370 | |||||||
chr11:62139392 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(64): Show |
114 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1291+387G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139392 | |||||||
chr11:62139463 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1291+458C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139463 | |||||||
chr11:62139473 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(62): Show |
111 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1291+468C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139473 | |||||||
chr11:62139630 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1292-604C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139630 | |||||||
chr11:62139712 | G | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(125): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1292-522G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139712 | |||||||
chr11:62139714 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1292-520G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139714 | |||||||
chr11:62139719 | A | G | 42 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0009 others(39): Show |
88 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1292-515A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139719 | |||||||
chr11:62139880 | T | C | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1292-354T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139880 | |||||||
chr11:62139968 | C | T | 1 | a0001c0023t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1292-266C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62139968 | |||||||
chr11:62140037 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1292-197C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140037 | |||||||
chr11:62140073 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0130 |
3 | HG01074.hp2 HG01192.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1292-161T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140073 | |||||||
chr11:62140091 | G | A | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1292-143G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140091 | |||||||
chr11:62140103 | C | T | 1 | a0001c0002t0001g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1292-131C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140103 | |||||||
chr11:62140122 | G | A | 1 | a0001c0038t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1292-112G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140122 | |||||||
chr11:62140151 | A | G | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1292-83A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140151 | |||||||
chr11:62140159 | T | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(48): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1292-75T>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 7/18 | chr11 | 62140159 | |||||||
chr11:62140349 | C | A | 8 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1343+64C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140349 | |||||||
chr11:62140437 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(122): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1343+152A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140437 | |||||||
chr11:62140482 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1343+197G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140482 | |||||||
chr11:62140493 | C | G | 1 | a0001c0001t0001g0018 | 4 | HG00423.hp1 HG02135.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343+208C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140493 | |||||||
chr11:62140497 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(56): Show |
104 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1344-207C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140497 | |||||||
chr11:62140550 | G | A | 8 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344-154G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140550 | |||||||
chr11:62140631 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0084 |
3 | HG02809.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1344-73G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140631 | |||||||
chr11:62140684 | C | T | 2 | a0002c0003t0002g0049 a0002c0003t0010g0049 |
2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1344-20C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 8/18 | chr11 | 62140684 | |||||||
chr11:62141052 | G | T | 8 | a0001c0010t0001g0057 a0001c0010t0001g0058 a0001c0010t0001g0059 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1593+8G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141052 | |||||||
chr11:62141065 | C | A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(2): Show |
6 | HG02145.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1593+21C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141065 | |||||||
chr11:62141074 | G | C | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(2): Show |
6 | HG02145.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1593+30G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141074 | |||||||
chr11:62141177 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1593+133C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141177 | |||||||
chr11:62141200 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(119): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1593+156G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141200 | |||||||
chr11:62141405 | G | A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0173 others(2): Show |
6 | HG02145.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1594-95G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141405 | |||||||
chr11:62141442 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1594-58G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 10/18 | chr11 | 62141442 | |||||||
chr11:62141563 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1605+52G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62141563 | |||||||
chr11:62141675 | C | A | 1 | a0003c0019t0003g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1605+164C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62141675 | |||||||
chr11:62141692 | C | A | 1 | a0001c0002t0001g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1605+181C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62141692 | |||||||
chr11:62142091 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(133): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1605+580A>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142091 | |||||||
chr11:62142117 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1605+606G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142117 | |||||||
chr11:62142132 | T | C | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
17 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1605+621T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142132 | |||||||
chr11:62142148 | T | C | 53 | a0001c0017t0004g0051 a0002c0003t0002g0003 a0002c0003t0002g0007 others(50): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1605+637T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142148 | |||||||
chr11:62142171 | A | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1605+660A>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142171 | |||||||
chr11:62142295 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(48): Show |
103 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1605+784C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142295 | |||||||
chr11:62142397 | C | T | 5 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+886C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142397 | |||||||
chr11:62142497 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(134): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1605+986A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142497 | |||||||
chr11:62142686 | CT | C | 18 | a0002c0003t0003g0013 a0003c0004t0003g0012 a0003c0004t0003g0013 others(15): Show |
30 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1605+1176delT | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142686 | |||||||
chr11:62142810 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1605+1299T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142810 | |||||||
chr11:62142879 | G | A | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | NA18952.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1605+1368G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142879 | |||||||
chr11:62142948 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1605+1437A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142948 | |||||||
chr11:62142964 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1605+1453A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62142964 | |||||||
chr11:62143003 | C | G | 1 | a0005c0008t0004g0179 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1605+1492C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143003 | |||||||
chr11:62143052 | G | GCCCACAC others(212): Show |
20 | a0001c0001t0001g0053 a0001c0001t0001g0095 a0001c0001t0001g0096 others(17): Show |
32 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1605+1543_1605+154 others(223): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62143052 | ||||||
chr11:62143052 | G | GCCCACAC others(212): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(44): Show |
89 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1605+1543_1605+154 others(223): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62143052 | ||||||
chr11:62143052 | G | GCCCACAC others(430): Show |
1 | a0001c0001t0001g0127 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1605+1543_1605+154 others(441): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62143052 | ||||||
chr11:62143052 | G | GCCCACAC others(212): Show |
1 | a0001c0001t0001g0038 | 2 | HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1605+1543_1605+154 others(223): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62143052 | ||||||
chr11:62143105 | T | C | 1 | a0021c0034t0001g0071 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1605+1594T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143105 | |||||||
chr11:62143274 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1606-1708A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143274 | |||||||
chr11:62143332 | C | T | 12 | a0001c0001t0001g0053 a0001c0006t0001g0005 a0001c0010t0001g0057 others(9): Show |
23 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1606-1650C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143332 | |||||||
chr11:62143603 | C | T | 1 | a0001c0035t0001g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1606-1379C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143603 | |||||||
chr11:62143618 | G | A | 1 | a0002c0003t0002g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1606-1364G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143618 | |||||||
chr11:62143725 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1606-1257G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143725 | |||||||
chr11:62143950 | C | T | 21 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(18): Show |
46 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1606-1032C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62143950 | |||||||
chr11:62144040 | G | A | 1 | a0002c0003t0002g0161 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1606-942G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144040 | |||||||
chr11:62144057 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(130): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1606-925T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144057 | |||||||
chr11:62144063 | A | G | 11 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(8): Show |
20 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1606-919A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144063 | |||||||
chr11:62144273 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1606-709A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144273 | |||||||
chr11:62144288 | C | T | 2 | a0009c0011t0001g0030 a0009c0011t0001g0031 |
4 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1606-694C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144288 | |||||||
chr11:62144330 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1606-652C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144330 | |||||||
chr11:62144335 | C | CAAAAAA | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1606-639_1606-634d others(8): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62144335 | ||||||
chr11:62144335 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(126): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1606-634delA | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62144335 | ||||||
chr11:62144338 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1606-644A>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144338 | |||||||
chr11:62144391 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1606-591A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144391 | |||||||
chr11:62144397 | AAATT | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
5 | HG02145.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1606-581_1606-578d others(6): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 62144397 | ||||||
chr11:62144565 | C | T | 2 | a0001c0001t0001g0029 a0023c0025t0001g0029 |
2 | HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1606-417C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144565 | |||||||
chr11:62144642 | C | T | 4 | a0001c0002t0001g0009 a0001c0002t0001g0072 a0001c0002t0001g0105 others(1): Show |
9 | NA18947.hp2 NA18957.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.1606-340C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144642 | |||||||
chr11:62144738 | C | T | 5 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1606-244C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144738 | |||||||
chr11:62144808 | C | T | 4 | a0001c0002t0001g0009 a0001c0002t0001g0072 a0001c0002t0001g0105 others(1): Show |
9 | NA18947.hp2 NA18957.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.1606-174C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144808 | |||||||
chr11:62144928 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1606-54G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 11/18 | chr11 | 62144928 | |||||||
chr11:62145369 | G | A | 1 | a0001c0024t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1836+80G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 13/18 | chr11 | 62145369 | |||||||
chr11:62145413 | G | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 |
3 | HG02647.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1836+124G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 13/18 | chr11 | 62145413 | |||||||
chr11:62145607 | C | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837-22C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 13/18 | chr11 | 62145607 | |||||||
chr11:62145619 | G | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0082 others(6): Show |
10 | HG00642.hp2 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1837-10G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 13/18 | chr11 | 62145619 | |||||||
chr11:62145760 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1959+9A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62145760 | |||||||
chr11:62145885 | G | T | 41 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(38): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1959+134G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62145885 | |||||||
chr11:62145890 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(46): Show |
92 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1959+139C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62145890 | |||||||
chr11:62145893 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1959+142G>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62145893 | |||||||
chr11:62145896 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1959+145G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62145896 | |||||||
chr11:62145924 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1959+173T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62145924 | |||||||
chr11:62146038 | C | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1959+287C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146038 | |||||||
chr11:62146139 | T | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(54): Show |
101 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1959+388T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146139 | |||||||
chr11:62146235 | A | G | 41 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(38): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1960-423A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146235 | |||||||
chr11:62146303 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0039 others(7): Show |
19 | HG00597.hp2 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1960-355G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146303 | |||||||
chr11:62146305 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1960-353G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146305 | |||||||
chr11:62146333 | A | G | 41 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(38): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1960-325A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146333 | |||||||
chr11:62146366 | G | T | 41 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(38): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1960-292G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146366 | |||||||
chr11:62146425 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1960-233C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146425 | |||||||
chr11:62146484 | C | T | 5 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1960-174C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146484 | |||||||
chr11:62146531 | G | A | 6 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(3): Show |
17 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1960-127G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146531 | |||||||
chr11:62146584 | G | A | 41 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(38): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1960-74G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146584 | |||||||
chr11:62146650 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1960-8T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 14/18 | chr11 | 62146650 | |||||||
chr11:62146922 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2204+20G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62146922 | |||||||
chr11:62146991 | T | C | 7 | a0001c0002t0001g0070 a0001c0017t0004g0051 a0005c0008t0004g0008 others(4): Show |
15 | HG01891.hp2 HG02055.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.2204+89T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62146991 | |||||||
chr11:62147061 | A | G | 1 | a0003c0004t0003g0019 | 4 | HG01261.hp1 HG01346.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2204+159A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147061 | |||||||
chr11:62147080 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2204+178A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147080 | |||||||
chr11:62147322 | A | G | 48 | a0001c0017t0004g0051 a0002c0003t0002g0003 a0002c0003t0002g0007 others(45): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2204+420A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147322 | |||||||
chr11:62147406 | C | T | 2 | a0001c0038t0001g0172 a0018c0032t0001g0169 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2204+504C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147406 | |||||||
chr11:62147419 | A | T | 42 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(39): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2204+517A>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147419 | |||||||
chr11:62147426 | A | G | 1 | a0012c0031t0009g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2204+524A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147426 | |||||||
chr11:62147497 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2204+595G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147497 | |||||||
chr11:62147503 | T | A | 48 | a0001c0017t0004g0051 a0002c0003t0002g0003 a0002c0003t0002g0007 others(45): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2204+601T>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147503 | |||||||
chr11:62147605 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(126): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2204+703T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147605 | |||||||
chr11:62147632 | C | T | 1 | a0006c0009t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2204+730C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147632 | |||||||
chr11:62147664 | G | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2204+762G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147664 | |||||||
chr11:62147675 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2204+773G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147675 | |||||||
chr11:62147680 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2204+778T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147680 | |||||||
chr11:62147730 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-746G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147730 | |||||||
chr11:62147804 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-672G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147804 | |||||||
chr11:62147868 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-608G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147868 | |||||||
chr11:62147907 | C | T | 1 | a0001c0002t0001g0103 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2205-569C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147907 | |||||||
chr11:62147917 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-559G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147917 | |||||||
chr11:62147966 | A | G | 2 | a0001c0002t0001g0068 a0001c0002t0008g0064 |
2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2205-510A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62147966 | |||||||
chr11:62148114 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-362T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62148114 | |||||||
chr11:62148229 | C | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-247C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62148229 | |||||||
chr11:62148278 | C | A | 6 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(3): Show |
17 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2205-198C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62148278 | |||||||
chr11:62148351 | A | G | 24 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(21): Show |
49 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2205-125A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62148351 | |||||||
chr11:62148435 | C | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2205-41C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62148435 | |||||||
chr11:62148449 | C | T | 1 | a0001c0010t0005g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2205-27C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 15/18 | chr11 | 62148449 | |||||||
chr11:62148574 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2283+20G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 16/18 | chr11 | 62148574 | |||||||
chr11:62148618 | C | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2283+64C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 16/18 | chr11 | 62148618 | |||||||
chr11:62148851 | C | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.2391+5C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62148851 | |||||||
chr11:62148852 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.2391+6A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62148852 | |||||||
chr11:62148981 | T | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2391+135T>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62148981 | |||||||
chr11:62149041 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2391+195A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149041 | |||||||
chr11:62149047 | C | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2391+201C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149047 | |||||||
chr11:62149083 | C | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2391+237C>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149083 | |||||||
chr11:62149147 | A | AAC | 5 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(2): Show |
13 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2391+311_2391+312d others(4): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 62149147 | ||||||
chr11:62149164 | CCTCT | C | 42 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(39): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2391+335_2391+338d others(6): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 62149164 | ||||||
chr11:62149246 | C | T | 42 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(39): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2391+400C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149246 | |||||||
chr11:62149258 | A | G | 5 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2391+412A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149258 | |||||||
chr11:62149261 | G | T | 1 | a0009c0011t0001g0031 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2391+415G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149261 | |||||||
chr11:62149330 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(135): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2391+484G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149330 | |||||||
chr11:62149383 | G | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2391+537G>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149383 | |||||||
chr11:62149386 | C | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2391+540C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149386 | |||||||
chr11:62149463 | G | A | 1 | a0002c0003t0002g0162 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2392-594G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149463 | |||||||
chr11:62149530 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(121): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2392-527A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149530 | |||||||
chr11:62149586 | A | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2392-471A>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149586 | |||||||
chr11:62149604 | C | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2392-453C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149604 | |||||||
chr11:62149669 | C | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2392-388C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149669 | |||||||
chr11:62149775 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2392-282G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149775 | |||||||
chr11:62149805 | C | T | 1 | a0001c0007t0001g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2392-252C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149805 | |||||||
chr11:62149968 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2392-89A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62149968 | |||||||
chr11:62150037 | G | A | 1 | a0016c0037t0002g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2392-20G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62150037 | |||||||
chr11:62150041 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2392-16A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 17/18 | chr11 | 62150041 | |||||||
chr11:62150370 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2542+163T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150370 | |||||||
chr11:62150459 | CTGGGCTT others(5): Show |
C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(46): Show |
92 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.2542+256_2542+267d others(14): Show |
INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 62150459 | ||||||
chr11:62150476 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(73): Show |
142 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2542+269A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150476 | |||||||
chr11:62150634 | A | G | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2542+427A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150634 | |||||||
chr11:62150651 | A | G | 4 | a0006c0009t0001g0034 a0006c0009t0001g0094 a0006c0009t0001g0109 others(1): Show |
5 | HG02280.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2542+444A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150651 | |||||||
chr11:62150661 | T | C | 48 | a0001c0017t0004g0051 a0002c0003t0002g0003 a0002c0003t0002g0007 others(45): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2542+454T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150661 | |||||||
chr11:62150740 | C | T | 1 | a0001c0002t0001g0032 | 2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2542+533C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150740 | |||||||
chr11:62150856 | T | C | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2542+649T>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150856 | |||||||
chr11:62150868 | C | T | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2542+661C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150868 | |||||||
chr11:62150938 | C | T | 1 | a0001c0001t0001g0017 | 4 | NA18971.hp2 NA19004.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.2542+731C>T | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150938 | |||||||
chr11:62150955 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2542+748G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150955 | |||||||
chr11:62150957 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2542+750G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62150957 | |||||||
chr11:62151147 | A | C | 6 | a0004c0005t0001g0006 a0004c0005t0001g0035 a0004c0005t0001g0111 others(3): Show |
17 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2543-615A>C | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151147 | |||||||
chr11:62151161 | G | A | 48 | a0001c0017t0004g0051 a0002c0003t0002g0003 a0002c0003t0002g0007 others(45): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2543-601G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151161 | |||||||
chr11:62151274 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(72): Show |
141 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.2543-488G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151274 | |||||||
chr11:62151402 | C | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2543-360C>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151402 | |||||||
chr11:62151445 | T | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(72): Show |
141 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.2543-317T>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151445 | |||||||
chr11:62151576 | G | A | 6 | a0001c0017t0004g0051 a0005c0008t0004g0008 a0005c0008t0004g0052 others(3): Show |
14 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2543-186G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151576 | |||||||
chr11:62151607 | G | A | 1 | a0010c0015t0005g0024 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2543-155G>A | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151607 | |||||||
chr11:62151725 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0084 |
3 | HG02809.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2543-37A>G | INCENP | ENSG00000149503.13 | transcript | ENST00000394818.8 | protein_coding | 18/18 | chr11 | 62151725 |