Item | Value |
---|---|
geneid | 100996521 |
ensemblid | ENSG00000283324.1 |
hgncid | 53440 |
symbol | CTXND2 |
name | cortexin domain containing 2 |
refseq_nuc | NM_001384189.2 |
refseq_prot | NP_001371118.1 |
ensembl_nuc | ENST00000636087.1 |
ensembl_prot | ENSP00000490418.1 |
mane_status | MANE Select |
chr | chr1 |
start | 150887136 |
end | 150913292 |
strand | + |
ver | v1.2 |
region | chr1:150887136-150913292 |
region5000 | chr1:150882136-150918292 |
regionname0 | CTXND2_chr1_150887136_150913292 |
regionname5000 | CTXND2_chr1_150882136_150918292 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 165 | 372 | 90 | 56 | 164 | 18 | 42 | CTXND2_chr1_150882136_150918292 | CTXND2 | ATGGA others(160): Show |
chr1 | 150882136 | 150918292 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1229 | 279 | 77 | 41 | 118 | 14 | 27 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0002 | 0/0 | 1229 | 74 | 0 | 14 | 45 | 4 | 11 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0003 | 0/0 | 1229 | 11 | 11 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0004 | 0/0 | 1229 | 3 | 0 | 0 | 0 | 0 | 3 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0005 | 0/0 | 1229 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0006 | 0/0 | 1229 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0007 | 0/0 | 1229 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0008 | 0/0 | 1229 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
a0001c0001t0009 | 0/0 | 1229 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | GAACT others(1224): Show |
chr1 | 150882136 | 150918292 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 19 | 1 | 2 | 13 | 1 | 2 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0002 | 0/0 | 14 | 0 | 2 | 10 | 0 | 2 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0004 | 0/0 | 7 | 2 | 1 | 3 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0008 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0009 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0004g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | FIN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0158 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03239 | hp1 | a0001 | c0001 | t0009 | g0181 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | YRI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | YRI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | GIH | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | GIH | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0182 | REF | REF | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | CTXND2_chr1_150882136_150918292 | CTXND2 | chr1 | 150882136 | 150918292 |
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 |
---|
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 |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150887161 | C | T | 1 | a0001c0001t0004 | 3 | HG02602.hp2 HG02683.hp2 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-226C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/2 | 25154 | chr1 | 150887161 | ||||||
chr1:150887277 | A | G | 1 | a0001c0001t0009 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/2 | 25038 | chr1 | 150887277 | ||||||
chr1:150912300 | G | A | 1 | a0001c0001t0002 | 74 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(71): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 2/2 | 15 | chr1 | 150912300 | ||||||
chr1:150912485 | T | C | 1 | a0001c0001t0005 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 2/2 | 3 | chr1 | 150912485 | ||||||
chr1:150912577 | T | C | 1 | a0001c0001t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 2/2 | 95 | chr1 | 150912577 | ||||||
chr1:150912948 | A | C | 1 | a0001c0001t0008 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 2/2 | 466 | chr1 | 150912948 | ||||||
chr1:150913074 | G | A | 1 | a0001c0001t0007 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 2/2 | 592 | chr1 | 150913074 | ||||||
chr1:150913237 | T | C | 1 | a0001c0001t0003 | 11 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*755T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 2/2 | 755 | chr1 | 150913237 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150887315 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | splice_donor_variant&intron_variant | HIGH | c.-74+2T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887315 | |||||||
chr1:150887321 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA19057.hp1 | splice_region_variant&intron_variant | LOW | c.-74+8A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887321 | |||||||
chr1:150887446 | T | TTTA | 3 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0002g0045 |
3 | HG02809.hp1 NA19003.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-74+157_-74+159dup others(3): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150887446 | ||||||
chr1:150887446 | TTTA | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
141 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-74+157_-74+159del others(3): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150887446 | ||||||
chr1:150887559 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-74+246T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887559 | |||||||
chr1:150887579 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
140 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.-74+266A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887579 | |||||||
chr1:150887710 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
140 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.-74+397G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887710 | |||||||
chr1:150887787 | AGTATTTT others(2540): Show |
A | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-74+478_-74+3024de others(1): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150887787 | ||||||
chr1:150887941 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-74+628G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887941 | |||||||
chr1:150887995 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(98): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-74+682C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150887995 | |||||||
chr1:150888069 | T | TA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
140 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.-74+764dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150888069 | ||||||
chr1:150888094 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-74+781C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888094 | |||||||
chr1:150888155 | T | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0164 |
2 | HG02071.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-74+842T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888155 | |||||||
chr1:150888217 | TTA | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
137 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.-74+906_-74+907del others(2): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150888217 | ||||||
chr1:150888219 | A | AT | 7 | a0001c0001t0001g0068 a0001c0001t0001g0085 a0001c0001t0001g0089 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+920dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150888219 | ||||||
chr1:150888219 | A | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(16): Show |
25 | HG01433.hp1 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-74+906A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888219 | |||||||
chr1:150888223 | T | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0132 |
3 | HG02615.hp1 NA18962.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-74+910T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888223 | |||||||
chr1:150888338 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-74+1025C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888338 | |||||||
chr1:150888415 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0129 |
2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-74+1102C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888415 | |||||||
chr1:150888464 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0103 |
4 | HG03017.hp2 HG03654.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+1151G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888464 | |||||||
chr1:150888753 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
134 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-74+1440C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888753 | |||||||
chr1:150888994 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-74+1681G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150888994 | |||||||
chr1:150889133 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0169 |
2 | HG01515.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.-74+1820G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150889133 | |||||||
chr1:150889268 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-74+1955C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150889268 | |||||||
chr1:150889383 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(45): Show |
62 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.-74+2070C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150889383 | |||||||
chr1:150889399 | C | CA | 16 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(13): Show |
17 | HG00738.hp1 HG01109.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-74+2102dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150889399 | ||||||
chr1:150889399 | CA | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
26 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-74+2102delA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150889399 | ||||||
chr1:150889484 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(111): Show |
164 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.-74+2171G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150889484 | |||||||
chr1:150889621 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
22 | HG01433.hp1 HG02109.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-74+2308C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150889621 | |||||||
chr1:150890394 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(15): Show |
24 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-74+3081G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150890394 | |||||||
chr1:150890415 | A | G | 8 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0175 others(5): Show |
10 | HG02056.hp1 HG02165.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.-74+3102A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150890415 | |||||||
chr1:150890882 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-74+3569T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150890882 | |||||||
chr1:150891174 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-74+3861G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891174 | |||||||
chr1:150891195 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-74+3882G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891195 | |||||||
chr1:150891202 | C | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-74+3889C>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891202 | |||||||
chr1:150891211 | C | CT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
139 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-74+3909dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150891211 | ||||||
chr1:150891340 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-74+4027A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891340 | |||||||
chr1:150891516 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4203T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891516 | |||||||
chr1:150891517 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4204C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891517 | |||||||
chr1:150891518 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4205T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891518 | |||||||
chr1:150891522 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4209A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891522 | |||||||
chr1:150891523 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4210T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891523 | |||||||
chr1:150891524 | T | G | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4211T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891524 | |||||||
chr1:150891526 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4213C>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891526 | |||||||
chr1:150891528 | A | T | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+4215A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891528 | |||||||
chr1:150891637 | T | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
141 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-74+4324T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891637 | |||||||
chr1:150891688 | T | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-74+4375T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891688 | |||||||
chr1:150891706 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-74+4393G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891706 | |||||||
chr1:150891729 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-74+4416C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150891729 | |||||||
chr1:150892203 | A | T | 1 | a0001c0001t0002g0031 | 2 | HG00280.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-74+4890A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892203 | |||||||
chr1:150892277 | T | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0063 a0001c0001t0002g0064 others(2): Show |
7 | NA18941.hp2 NA18999.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+4964T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892277 | |||||||
chr1:150892471 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-74+5158A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892471 | |||||||
chr1:150892511 | G | GTCT | 4 | a0001c0001t0001g0035 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
5 | NA18939.hp1 NA18966.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+5200_-74+5202d others(5): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150892511 | ||||||
chr1:150892516 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(112): Show |
165 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-74+5203A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892516 | |||||||
chr1:150892528 | C | CT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(21): Show |
45 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-74+5235dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150892528 | ||||||
chr1:150892528 | CT | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-74+5235delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150892528 | ||||||
chr1:150892528 | CTT | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
13 | HG01070.hp2 HG01169.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-74+5234_-74+5235d others(4): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150892528 | ||||||
chr1:150892528 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-74+5226_-74+5235d others(12): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150892528 | ||||||
chr1:150892531 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
133 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.-74+5218T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892531 | |||||||
chr1:150892532 | T | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0192 others(5): Show |
9 | HG00280.hp1 HG01192.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-74+5219T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892532 | |||||||
chr1:150892608 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
139 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-74+5295G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892608 | |||||||
chr1:150892719 | T | G | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+5406T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892719 | |||||||
chr1:150892790 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-74+5477C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892790 | |||||||
chr1:150892860 | C | A | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-74+5547C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892860 | |||||||
chr1:150892879 | G | A | 1 | a0001c0001t0005g0184 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-74+5566G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150892879 | |||||||
chr1:150893107 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-74+5794T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893107 | |||||||
chr1:150893161 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-74+5848T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893161 | |||||||
chr1:150893284 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
132 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-74+5971A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893284 | |||||||
chr1:150893515 | G | C | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6202G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893515 | |||||||
chr1:150893516 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6203T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893516 | |||||||
chr1:150893517 | G | C | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6204G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893517 | |||||||
chr1:150893518 | A | T | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6205A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893518 | |||||||
chr1:150893519 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6206T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893519 | |||||||
chr1:150893521 | C | A | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6208C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893521 | |||||||
chr1:150893523 | A | C | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6210A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893523 | |||||||
chr1:150893524 | T | G | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6211T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893524 | |||||||
chr1:150893526 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6213A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893526 | |||||||
chr1:150893529 | G | T | 1 | a0001c0001t0002g0062 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-74+6216G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893529 | |||||||
chr1:150893782 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-74+6469C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893782 | |||||||
chr1:150893816 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-74+6503A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150893816 | |||||||
chr1:150893984 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
138 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-74+6680dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150893984 | ||||||
chr1:150894007 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0191 |
3 | NA18966.hp2 NA18981.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-74+6694G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150894007 | |||||||
chr1:150894010 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-74+6697G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150894010 | |||||||
chr1:150894293 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-74+6980G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150894293 | |||||||
chr1:150894357 | G | A | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-74+7044G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150894357 | |||||||
chr1:150894904 | G | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
22 | HG01433.hp1 HG02109.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-74+7591G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150894904 | |||||||
chr1:150894985 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-74+7672C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150894985 | |||||||
chr1:150895026 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-74+7713G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895026 | |||||||
chr1:150895054 | C | CAT | 3 | a0001c0001t0001g0154 a0001c0001t0002g0076 a0001c0001t0002g0077 |
3 | HG02129.hp1 HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-74+7754_-74+7755d others(4): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150895054 | ||||||
chr1:150895054 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-74+7741C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895054 | |||||||
chr1:150895226 | T | A | 2 | a0001c0001t0003g0138 a0001c0001t0003g0139 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-74+7913T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895226 | |||||||
chr1:150895241 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-74+7928A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895241 | |||||||
chr1:150895312 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-74+7999C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895312 | |||||||
chr1:150895491 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03492.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-74+8178G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895491 | |||||||
chr1:150895558 | G | C | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-74+8245G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895558 | |||||||
chr1:150895607 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-74+8294G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895607 | |||||||
chr1:150895626 | C | A | 22 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0069 others(19): Show |
23 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-74+8313C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895626 | |||||||
chr1:150895629 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0262 |
4 | NA18944.hp2 NA18977.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+8316G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895629 | |||||||
chr1:150895642 | C | T | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-74+8329C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895642 | |||||||
chr1:150895696 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-74+8383G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895696 | |||||||
chr1:150895753 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-74+8440T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895753 | |||||||
chr1:150895806 | A | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(21): Show |
45 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-74+8493A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895806 | |||||||
chr1:150895836 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-74+8523C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895836 | |||||||
chr1:150895849 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-74+8536G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150895849 | |||||||
chr1:150896342 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-74+9029A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150896342 | |||||||
chr1:150896569 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(112): Show |
165 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-74+9256T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150896569 | |||||||
chr1:150896880 | AT | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG02109.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-74+9569delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150896880 | ||||||
chr1:150896953 | G | C | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-74+9640G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150896953 | |||||||
chr1:150897063 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-74+9750A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897063 | |||||||
chr1:150897343 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0256 |
3 | HG01074.hp2 HG01516.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-74+10030C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897343 | |||||||
chr1:150897353 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(108): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-74+10040G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897353 | |||||||
chr1:150897364 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(15): Show |
24 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-74+10051G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897364 | |||||||
chr1:150897392 | T | C | 54 | a0001c0001t0001g0100 a0001c0001t0002g0003 a0001c0001t0002g0007 others(51): Show |
73 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-74+10079T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897392 | |||||||
chr1:150897429 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-74+10116A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897429 | |||||||
chr1:150897485 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-74+10172G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897485 | |||||||
chr1:150897536 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | NA18946.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-74+10223C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897536 | |||||||
chr1:150897974 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
139 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-74+10661T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150897974 | |||||||
chr1:150898052 | T | G | 9 | a0001c0001t0003g0016 a0001c0001t0003g0138 a0001c0001t0003g0139 others(6): Show |
11 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-74+10739T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898052 | |||||||
chr1:150898068 | A | C | 1 | a0001c0001t0001g0032 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-74+10755A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898068 | |||||||
chr1:150898153 | G | GT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
141 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-74+10851dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150898153 | ||||||
chr1:150898153 | G | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(15): Show |
24 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-74+10840G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898153 | |||||||
chr1:150898202 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-74+10889G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898202 | |||||||
chr1:150898286 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+10973A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898286 | |||||||
chr1:150898528 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-74+11215C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898528 | |||||||
chr1:150898628 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0029 others(15): Show |
38 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-74+11315C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898628 | |||||||
chr1:150898654 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18994.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-74+11341A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898654 | |||||||
chr1:150898697 | A | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-74+11384A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898697 | |||||||
chr1:150898754 | C | CA | 44 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0050 others(41): Show |
49 | HG00280.hp2 HG00438.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-74+11457dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150898754 | ||||||
chr1:150898821 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(112): Show |
165 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-74+11508C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898821 | |||||||
chr1:150898848 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-74+11535C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898848 | |||||||
chr1:150898852 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0191 |
3 | NA18966.hp2 NA18981.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-74+11539C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898852 | |||||||
chr1:150898870 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-74+11557G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898870 | |||||||
chr1:150898921 | C | CA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(89): Show |
139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-74+11619dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150898921 | ||||||
chr1:150898921 | C | CAA | 44 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(41): Show |
61 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-74+11618_-74+1161 others(6): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150898921 | ||||||
chr1:150898927 | A | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0092 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-74+11614A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898927 | |||||||
chr1:150898929 | A | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0028 others(22): Show |
42 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-74+11616A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898929 | |||||||
chr1:150898931 | A | AAT | 14 | a0001c0001t0001g0049 a0001c0001t0001g0126 a0001c0001t0001g0196 others(11): Show |
16 | HG00323.hp2 HG01928.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.-74+11635_-74+1163 others(6): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150898931 | ||||||
chr1:150898931 | A | AT | 3 | a0001c0001t0002g0045 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | HG01192.hp2 HG02129.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-74+11618_-74+1161 others(5): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898931 | |||||||
chr1:150898931 | A | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-74+11618A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898931 | |||||||
chr1:150898933 | T | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
113 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-74+11620T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898933 | |||||||
chr1:150898935 | T | A | 2 | a0001c0001t0001g0208 a0001c0001t0002g0187 |
2 | HG02132.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-74+11622T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898935 | |||||||
chr1:150898958 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-74+11645C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150898958 | |||||||
chr1:150899097 | C | CAAAT | 17 | a0001c0001t0001g0089 a0001c0001t0001g0100 a0001c0001t0001g0157 others(14): Show |
22 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-74+11816_-74+1181 others(8): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150899097 | ||||||
chr1:150899097 | CAAAT | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0029 others(16): Show |
39 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-74+11816_-74+1181 others(8): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150899097 | ||||||
chr1:150899121 | TAAATAAA others(5): Show |
T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
146 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-74+11812_-74+1182 others(16): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150899121 | ||||||
chr1:150899125 | TAAATAAA others(1): Show |
T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
16 | HG01433.hp1 HG02109.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-74+11816_-74+1182 others(12): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150899125 | ||||||
chr1:150899129 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-74+11816T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150899129 | |||||||
chr1:150899129 | TAAAC | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(21): Show |
31 | HG01257.hp2 HG02055.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.-74+11827_-74+1183 others(8): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150899129 | ||||||
chr1:150899133 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(101): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-74+11820C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150899133 | |||||||
chr1:150899515 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0253 |
3 | HG01167.hp1 HG01169.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-74+12202A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150899515 | |||||||
chr1:150899833 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0078 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-73-12409G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150899833 | |||||||
chr1:150899922 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-73-12320T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150899922 | |||||||
chr1:150900034 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-73-12208C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900034 | |||||||
chr1:150900081 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-73-12161C>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900081 | |||||||
chr1:150900085 | A | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-73-12157A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900085 | |||||||
chr1:150900091 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-73-12151C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900091 | |||||||
chr1:150900169 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-73-12073G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900169 | |||||||
chr1:150900173 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-73-12069C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900173 | |||||||
chr1:150900181 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-73-12061C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900181 | |||||||
chr1:150900204 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0103 |
4 | HG03017.hp2 HG03654.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-12038C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900204 | |||||||
chr1:150900225 | T | C | 8 | a0001c0001t0003g0016 a0001c0001t0003g0138 a0001c0001t0003g0139 others(5): Show |
10 | HG02055.hp1 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-12017T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900225 | |||||||
chr1:150900388 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
6 | NA18944.hp1 NA18946.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-11854A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900388 | |||||||
chr1:150900460 | G | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG01175.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-73-11782G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900460 | |||||||
chr1:150900571 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-11671C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900571 | |||||||
chr1:150900657 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
138 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-73-11576delA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150900657 | ||||||
chr1:150900673 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-73-11569C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900673 | |||||||
chr1:150900720 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-11522A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900720 | |||||||
chr1:150900730 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-11512T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900730 | |||||||
chr1:150900760 | G | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-11482G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900760 | |||||||
chr1:150900848 | G | C | 1 | a0001c0001t0002g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-73-11394G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900848 | |||||||
chr1:150900881 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-73-11361A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900881 | |||||||
chr1:150900883 | A | C | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-11359A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900883 | |||||||
chr1:150900913 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-73-11329G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900913 | |||||||
chr1:150900917 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-73-11325C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900917 | |||||||
chr1:150900927 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-73-11315C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900927 | |||||||
chr1:150900953 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-11289T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150900953 | |||||||
chr1:150901085 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-73-11157C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901085 | |||||||
chr1:150901192 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-73-11050C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901192 | |||||||
chr1:150901205 | ATTC | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(108): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-73-11034_-73-1103 others(7): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150901205 | ||||||
chr1:150901239 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-73-11003A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901239 | |||||||
chr1:150901270 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-73-10972A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901270 | |||||||
chr1:150901281 | G | A | 8 | a0001c0001t0003g0016 a0001c0001t0003g0138 a0001c0001t0003g0139 others(5): Show |
10 | HG02055.hp1 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-10961G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901281 | |||||||
chr1:150901333 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-73-10909T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901333 | |||||||
chr1:150901685 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-10557C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901685 | |||||||
chr1:150901686 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-73-10556G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901686 | |||||||
chr1:150901795 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-73-10447G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150901795 | |||||||
chr1:150901880 | TGCACTCC others(1): Show |
T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
139 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-73-10351_-73-1034 others(12): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150901880 | ||||||
chr1:150901924 | T | TA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0058 others(3): Show |
7 | HG02572.hp1 HG03225.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-10305dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150901924 | ||||||
chr1:150902016 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-73-10226A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902016 | |||||||
chr1:150902123 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-73-10119T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902123 | |||||||
chr1:150902124 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-73-10118G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902124 | |||||||
chr1:150902130 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0248 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-73-10112C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902130 | |||||||
chr1:150902144 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
132 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-73-10098G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902144 | |||||||
chr1:150902162 | G | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0007g0156 |
3 | HG02145.hp2 HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-73-10080G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902162 | |||||||
chr1:150902172 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-73-10070C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902172 | |||||||
chr1:150902338 | C | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG02109.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-9904C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902338 | |||||||
chr1:150902404 | CA | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0196 others(5): Show |
8 | HG02572.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73-9823delA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150902404 | ||||||
chr1:150902556 | G | A | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-9686G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902556 | |||||||
chr1:150902562 | G | C | 3 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0143 |
3 | HG02055.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-73-9680G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902562 | |||||||
chr1:150902598 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-73-9644G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902598 | |||||||
chr1:150902639 | C | T | 1 | a0001c0001t0002g0026 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-73-9603C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902639 | |||||||
chr1:150902697 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(112): Show |
165 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-73-9545C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902697 | |||||||
chr1:150902792 | A | C | 1 | a0001c0001t0003g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-73-9450A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150902792 | |||||||
chr1:150903050 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-73-9192A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903050 | |||||||
chr1:150903065 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-73-9177C>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903065 | |||||||
chr1:150903139 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-73-9103C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903139 | |||||||
chr1:150903337 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-73-8905C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903337 | |||||||
chr1:150903491 | A | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(98): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-73-8751A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903491 | |||||||
chr1:150903671 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-73-8571G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903671 | |||||||
chr1:150903796 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-73-8446G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903796 | |||||||
chr1:150903800 | C | CA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0159 others(5): Show |
11 | HG00621.hp1 HG00738.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-73-8427dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150903800 | ||||||
chr1:150903800 | CA | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(14): Show |
23 | HG00140.hp2 HG01099.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-73-8427delA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150903800 | ||||||
chr1:150903874 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-73-8368G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150903874 | |||||||
chr1:150904090 | G | T | 1 | a0001c0001t0002g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-73-8152G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150904090 | |||||||
chr1:150904174 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-73-8068C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150904174 | |||||||
chr1:150904442 | C | G | 1 | a0001c0001t0002g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-73-7800C>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150904442 | |||||||
chr1:150904460 | A | G | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-7782A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150904460 | |||||||
chr1:150904561 | T | C | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-7681T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150904561 | |||||||
chr1:150904870 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-73-7372G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150904870 | |||||||
chr1:150905042 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
7 | NA18954.hp2 NA18967.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73-7200C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905042 | |||||||
chr1:150905062 | C | CCA | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
68 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-73-7139_-73-7138d others(4): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905062 | C | CCACA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(33): Show |
41 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.-73-7141_-73-7138d others(6): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905062 | C | CCACACA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-73-7143_-73-7138d others(8): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905062 | C | CCACACAC others(5): Show |
1 | a0001c0001t0001g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-73-7149_-73-7138d others(14): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905062 | CCA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
127 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-73-7139_-73-7138d others(4): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905062 | CCACA | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(34): Show |
45 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-73-7141_-73-7138d others(6): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905062 | CCACACA | C | 4 | a0001c0001t0001g0004 a0001c0001t0003g0138 a0001c0001t0003g0151 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-7143_-73-7138d others(8): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905062 | ||||||
chr1:150905070 | A | C | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-7172A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905070 | |||||||
chr1:150905105 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-73-7137A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905105 | |||||||
chr1:150905143 | C | CT | 13 | a0001c0001t0001g0088 a0001c0001t0001g0124 a0001c0001t0001g0155 others(10): Show |
13 | HG01192.hp2 HG01361.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-7080dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905143 | ||||||
chr1:150905143 | CT | C | 8 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0185 others(5): Show |
8 | HG01975.hp1 HG02896.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-7080delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905143 | ||||||
chr1:150905205 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0029 others(15): Show |
38 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-73-7037G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905205 | |||||||
chr1:150905221 | G | C | 5 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | NA18953.hp1 NA19059.hp1 NA19059.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-7021G>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905221 | |||||||
chr1:150905363 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0223 a0001c0001t0001g0224 |
4 | HG01099.hp1 HG01123.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-6879C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905363 | |||||||
chr1:150905364 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73-6878G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905364 | |||||||
chr1:150905383 | A | AT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
138 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-73-6858dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905383 | ||||||
chr1:150905433 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-73-6809G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905433 | |||||||
chr1:150905623 | TC | T | 25 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0061 others(22): Show |
28 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-73-6617delC | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150905623 | ||||||
chr1:150905716 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-73-6526C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905716 | |||||||
chr1:150905757 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-6485G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905757 | |||||||
chr1:150905818 | A | G | 1 | a0001c0001t0001g0024 | 2 | NA18977.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-73-6424A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905818 | |||||||
chr1:150905847 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0222 |
6 | HG01361.hp2 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-6395G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905847 | |||||||
chr1:150905893 | G | A | 1 | a0001c0001t0008g0158 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-73-6349G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905893 | |||||||
chr1:150905915 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0170 |
4 | HG01891.hp1 NA18944.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-6327G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905915 | |||||||
chr1:150905969 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-73-6273G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905969 | |||||||
chr1:150905977 | G | A | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-6265G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150905977 | |||||||
chr1:150906173 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0086 a0001c0001t0001g0087 |
4 | HG01243.hp2 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-6069C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150906173 | |||||||
chr1:150906291 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-73-5951C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150906291 | |||||||
chr1:150906613 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-73-5629A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150906613 | |||||||
chr1:150906625 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
138 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-73-5617A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150906625 | |||||||
chr1:150906728 | C | A | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-5514C>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150906728 | |||||||
chr1:150906773 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01255.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-73-5469C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150906773 | |||||||
chr1:150907004 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-73-5238T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907004 | |||||||
chr1:150907088 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-73-5154A>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907088 | |||||||
chr1:150907252 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-73-4990A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907252 | |||||||
chr1:150907691 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0238 a0001c0001t0004g0017 |
5 | HG02602.hp2 HG02683.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-4551C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907691 | |||||||
chr1:150907700 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-73-4542G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907700 | |||||||
chr1:150907704 | CT | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-73-4515delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150907704 | ||||||
chr1:150907704 | CTT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
128 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-73-4516_-73-4515d others(4): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150907704 | ||||||
chr1:150907883 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-73-4359G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907883 | |||||||
chr1:150907899 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-73-4343T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907899 | |||||||
chr1:150907909 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-73-4333C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150907909 | |||||||
chr1:150908011 | C | CT | 12 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0060 others(9): Show |
12 | HG01975.hp2 HG02071.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-73-4215dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150908011 | ||||||
chr1:150908011 | CTT | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0051 others(2): Show |
7 | HG02896.hp1 HG03209.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-4216_-73-4215d others(4): Show |
CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150908011 | ||||||
chr1:150908147 | T | A | 1 | a0001c0001t0002g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-73-4095T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908147 | |||||||
chr1:150908241 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-73-4001G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908241 | |||||||
chr1:150908284 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-73-3958G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908284 | |||||||
chr1:150908392 | T | A | 1 | a0001c0001t0003g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-73-3850T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908392 | |||||||
chr1:150908430 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-73-3812A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908430 | |||||||
chr1:150908596 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-73-3646T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908596 | |||||||
chr1:150908790 | T | TA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
135 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.-73-3439dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150908790 | ||||||
chr1:150908790 | TA | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0126 a0001c0001t0001g0133 others(3): Show |
6 | HG00323.hp2 HG02976.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-3439delA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150908790 | ||||||
chr1:150908838 | G | T | 1 | a0001c0001t0003g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-73-3404G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908838 | |||||||
chr1:150908932 | A | G | 1 | a0001c0001t0006g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-73-3310A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150908932 | |||||||
chr1:150909006 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0078 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-73-3236A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909006 | |||||||
chr1:150909095 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-73-3147C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909095 | |||||||
chr1:150909111 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(15): Show |
24 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-73-3131G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909111 | |||||||
chr1:150909170 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-73-3072A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909170 | |||||||
chr1:150909187 | G | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(99): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-73-3055G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909187 | |||||||
chr1:150909237 | C | CA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(95): Show |
146 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.-73-2986dupA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150909237 | ||||||
chr1:150909237 | CA | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0127 a0001c0001t0001g0137 others(3): Show |
6 | HG01069.hp2 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-2986delA | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150909237 | ||||||
chr1:150909356 | T | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG02109.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-2886T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909356 | |||||||
chr1:150909826 | C | T | 1 | a0001c0001t0009g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-2416C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150909826 | |||||||
chr1:150910112 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0191 |
3 | NA18966.hp2 NA18981.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-73-2130T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910112 | |||||||
chr1:150910120 | GT | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0053 others(2): Show |
6 | HG02451.hp2 HG02738.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-2110delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150910120 | ||||||
chr1:150910133 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0002g0120 |
2 | HG01192.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-73-2109C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910133 | |||||||
chr1:150910138 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-73-2104T>C | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910138 | |||||||
chr1:150910164 | C | T | 7 | a0001c0001t0002g0025 a0001c0001t0002g0098 a0001c0001t0002g0099 others(4): Show |
8 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73-2078C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910164 | |||||||
chr1:150910318 | T | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0082 |
3 | NA18978.hp2 NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-73-1924T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910318 | |||||||
chr1:150910334 | TG | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(71): Show |
114 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-73-1906delG | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150910334 | ||||||
chr1:150910373 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-1869G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910373 | |||||||
chr1:150910561 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(111): Show |
164 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.-73-1681C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910561 | |||||||
chr1:150910618 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-73-1624T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910618 | |||||||
chr1:150910630 | A | AT | 12 | a0001c0001t0001g0050 a0001c0001t0001g0085 a0001c0001t0001g0124 others(9): Show |
12 | HG00438.hp1 HG00735.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-73-1593dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150910630 | ||||||
chr1:150910630 | AT | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(24): Show |
34 | HG00323.hp1 HG01070.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.-73-1593delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150910630 | ||||||
chr1:150910729 | T | G | 7 | a0001c0001t0001g0185 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG02109.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-1513T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910729 | |||||||
chr1:150910866 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-1376G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910866 | |||||||
chr1:150910886 | G | T | 1 | a0001c0001t0001g0042 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-73-1356G>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910886 | |||||||
chr1:150910922 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-73-1320A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910922 | |||||||
chr1:150910956 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-73-1286C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150910956 | |||||||
chr1:150911191 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-73-1051G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911191 | |||||||
chr1:150911373 | CT | C | 3 | a0001c0001t0001g0130 a0001c0001t0002g0112 a0001c0001t0002g0174 |
3 | NA18968.hp1 NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.-73-864delT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150911373 | ||||||
chr1:150911441 | A | AT | 11 | a0001c0001t0001g0040 a0001c0001t0001g0145 a0001c0001t0001g0168 others(8): Show |
12 | HG01070.hp1 HG01071.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73-789dupT | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | 150911441 | ||||||
chr1:150911441 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-801A>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911441 | |||||||
chr1:150911446 | T | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0129 |
2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-73-796T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911446 | |||||||
chr1:150911474 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-73-768T>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911474 | |||||||
chr1:150911476 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-73-766C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911476 | |||||||
chr1:150911504 | C | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
6 | HG00621.hp2 NA18939.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-738C>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911504 | |||||||
chr1:150911653 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-73-589G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911653 | |||||||
chr1:150911795 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(223): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.-73-447A>G | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911795 | |||||||
chr1:150911964 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-73-278C>T | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911964 | |||||||
chr1:150911987 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-73-255G>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150911987 | |||||||
chr1:150912117 | T | A | 1 | a0001c0001t0002g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-73-125T>A | CTXND2 | ENSG00000283324.1 | transcript | ENST00000636087.1 | protein_coding | 1/1 | chr1 | 150912117 |