Item | Value |
---|---|
geneid | 63922 |
ensemblid | ENSG00000127586.17 |
hgncid | 18435 |
symbol | CHTF18 |
name | chromosome transmission fidelity factor 18 |
refseq_nuc | NM_022092.3 |
refseq_prot | NP_071375.1 |
ensembl_nuc | ENST00000262315.14 |
ensembl_prot | ENSP00000262315.9 |
mane_status | MANE Select |
chr | chr16 |
start | 788620 |
end | 798074 |
strand | + |
ver | v1.2 |
region | chr16:788620-798074 |
region5000 | chr16:783620-803074 |
regionname0 | CHTF18_chr16_788620_798074 |
regionname5000 | CHTF18_chr16_783620_803074 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 975 | 149 | 14 | 43 | 61 | 12 | 18 | 43 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0002 | 0/1 | 975 | 67 | 0 | 7 | 49 | 4 | 6 | 40 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0003 | 0/0 | 975 | 55 | 11 | 6 | 37 | 0 | 1 | 29 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0004 | 0/0 | 975 | 21 | 8 | 5 | 3 | 0 | 5 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0005 | 0/0 | 975 | 18 | 13 | 1 | 0 | 1 | 3 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0006 | 0/0 | 975 | 14 | 0 | 1 | 8 | 0 | 5 | 7 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0007 | 0/0 | 975 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0008 | 0/0 | 975 | 8 | 0 | 8 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0009 | 0/0 | 975 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0010 | 0/0 | 975 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0011 | 0/0 | 975 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0012 | 0/0 | 975 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0013 | 0/0 | 975 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0014 | 0/0 | 975 | 3 | 0 | 1 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0015 | 0/0 | 975 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0016 | 0/0 | 975 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0017 | 0/0 | 975 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0018 | 0/0 | 975 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0019 | 0/0 | 975 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0020 | 0/0 | 975 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0021 | 0/0 | 975 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0022 | 0/0 | 975 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0023 | 0/0 | 975 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0024 | 0/0 | 975 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0025 | 0/0 | 975 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0026 | 0/0 | 975 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0027 | 0/0 | 975 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0028 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0029 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0030 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0031 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0032 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0033 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0034 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0035 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0036 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0037 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0038 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0039 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0040 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0041 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0042 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0043 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0044 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0045 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0046 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0047 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0048 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0049 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0050 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0051 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0052 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(970): Show |
chr16 | 783620 | 803074 |
a0053 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | MEDYE others(610): Show |
chr16 | 783620 | 803074 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2925 | 130 | 5 | 42 | 60 | 9 | 14 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0009 | 0/0 | 2925 | 6 | 6 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0016 | 0/0 | 2925 | 4 | 0 | 0 | 0 | 2 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0024 | 0/0 | 2925 | 3 | 0 | 1 | 0 | 1 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0032 | 1/0 | 2925 | 2 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0034 | 0/0 | 2925 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0057 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0001c0058 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0002c0002 | 0/1 | 2925 | 60 | 0 | 4 | 45 | 4 | 6 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0002c0039 | 0/0 | 2925 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0002c0040 | 0/0 | 2925 | 2 | 0 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0002c0075 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0002c0078 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0002c0079 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0003 | 0/0 | 2925 | 33 | 0 | 3 | 30 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0007 | 0/0 | 2925 | 11 | 5 | 3 | 2 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0017 | 0/0 | 2925 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0028 | 0/0 | 2925 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0067 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0070 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0072 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0003c0073 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0004c0005 | 0/0 | 2925 | 13 | 2 | 4 | 2 | 0 | 5 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0004c0013 | 0/0 | 2925 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0004c0021 | 0/0 | 2925 | 3 | 2 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0004c0048 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0005c0004 | 0/0 | 2925 | 18 | 13 | 1 | 0 | 1 | 3 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0006c0006 | 0/0 | 2925 | 13 | 0 | 1 | 7 | 0 | 5 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0006c0051 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0007c0012 | 0/0 | 2925 | 5 | 5 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0007c0030 | 0/0 | 2925 | 3 | 2 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0008c0008 | 0/0 | 2925 | 8 | 0 | 8 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0009c0011 | 0/0 | 2925 | 5 | 5 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0009c0027 | 0/0 | 2925 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0010c0010 | 0/0 | 2925 | 5 | 0 | 0 | 5 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0010c0064 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0011c0020 | 0/0 | 2925 | 3 | 1 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0011c0031 | 0/0 | 2925 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0012c0015 | 0/0 | 2925 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0013c0014 | 0/0 | 2925 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0014c0029 | 0/0 | 2925 | 3 | 0 | 1 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0015c0025 | 0/0 | 2925 | 3 | 0 | 3 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0016c0023 | 0/0 | 2925 | 3 | 0 | 1 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0017c0022 | 0/0 | 2925 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0018c0019 | 0/0 | 2925 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0019c0026 | 0/0 | 2925 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0020c0018 | 0/0 | 2925 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0021c0036 | 0/0 | 2925 | 2 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0022c0035 | 0/0 | 2925 | 2 | 0 | 0 | 0 | 1 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0023c0038 | 0/0 | 2925 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0024c0042 | 0/0 | 2925 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0025c0041 | 0/0 | 2925 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0026c0037 | 0/0 | 2925 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0027c0033 | 0/0 | 2925 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0028c0045 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0029c0055 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0030c0074 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0031c0077 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0032c0052 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0033c0066 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0034c0043 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0035c0060 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0036c0044 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0037c0069 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0038c0068 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0039c0062 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0040c0047 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0041c0046 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0042c0071 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0043c0054 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0044c0080 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0045c0049 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0046c0053 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0047c0056 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0048c0063 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0049c0061 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0050c0065 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0051c0050 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0052c0059 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2920): Show |
chr16 | 783620 | 803074 | ||
a0053c0076 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | ATGGA others(2930): Show |
chr16 | 783620 | 803074 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3092 | 128 | 4 | 42 | 60 | 8 | 14 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0001t0005 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0001t0008 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0009t0001 | 0/0 | 3092 | 6 | 6 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0016t0001 | 0/0 | 3092 | 4 | 0 | 0 | 0 | 2 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0024t0001 | 0/0 | 3092 | 3 | 0 | 1 | 0 | 1 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0032t0001 | 1/0 | 3092 | 2 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0034t0002 | 0/0 | 3092 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0057t0001 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0001c0058t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0002c0002t0001 | 0/1 | 3092 | 60 | 0 | 4 | 45 | 4 | 6 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0002c0039t0001 | 0/0 | 3092 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0002c0040t0001 | 0/0 | 3092 | 2 | 0 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0002c0075t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0002c0078t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0002c0079t0001 | 0/0 | 3092 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0003t0001 | 0/0 | 3092 | 33 | 0 | 3 | 30 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0007t0001 | 0/0 | 3092 | 10 | 5 | 3 | 1 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0007t0006 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0017t0001 | 0/0 | 3092 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0028t0001 | 0/0 | 3092 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0067t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0070t0002 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0072t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0003c0073t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0004c0005t0002 | 0/0 | 3092 | 13 | 2 | 4 | 2 | 0 | 5 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0004c0013t0002 | 0/0 | 3092 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0004c0021t0001 | 0/0 | 3092 | 3 | 2 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0004c0048t0002 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0005c0004t0001 | 0/0 | 3092 | 18 | 13 | 1 | 0 | 1 | 3 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0006c0006t0001 | 0/0 | 3092 | 13 | 0 | 1 | 7 | 0 | 5 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0006c0051t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0007c0012t0003 | 0/0 | 3092 | 5 | 5 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0007c0030t0002 | 0/0 | 3092 | 3 | 2 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0008c0008t0001 | 0/0 | 3092 | 8 | 0 | 8 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0009c0011t0001 | 0/0 | 3092 | 5 | 5 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0009c0027t0001 | 0/0 | 3092 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0010c0010t0001 | 0/0 | 3092 | 5 | 0 | 0 | 5 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0010c0064t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0011c0020t0001 | 0/0 | 3092 | 3 | 1 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0011c0031t0001 | 0/0 | 3092 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0012c0015t0001 | 0/0 | 3092 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0013c0014t0001 | 0/0 | 3092 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0014c0029t0001 | 0/0 | 3092 | 3 | 0 | 1 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0015c0025t0001 | 0/0 | 3092 | 3 | 0 | 3 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0016c0023t0001 | 0/0 | 3092 | 3 | 0 | 1 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0017c0022t0001 | 0/0 | 3092 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0018c0019t0001 | 0/0 | 3092 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0019c0026t0001 | 0/0 | 3092 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0020c0018t0001 | 0/0 | 3092 | 3 | 3 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0021c0036t0004 | 0/0 | 3092 | 2 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0022c0035t0001 | 0/0 | 3092 | 2 | 0 | 0 | 0 | 1 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0023c0038t0001 | 0/0 | 3092 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0024c0042t0001 | 0/0 | 3092 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0025c0041t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0025c0041t0007 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0026c0037t0001 | 0/0 | 3092 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0027c0033t0001 | 0/0 | 3092 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0028c0045t0001 | 0/0 | 3092 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0029c0055t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0030c0074t0001 | 0/0 | 3092 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0031c0077t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0032c0052t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0033c0066t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0034c0043t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0035c0060t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0036c0044t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0037c0069t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0038c0068t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0039c0062t0001 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0040c0047t0002 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0041c0046t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0042c0071t0001 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0043c0054t0001 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0044c0080t0001 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0045c0049t0001 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0046c0053t0001 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0047c0056t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0048c0063t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0049c0061t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0050c0065t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0051c0050t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0052c0059t0001 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3087): Show |
chr16 | 783620 | 803074 |
a0053c0076t0001 | 0/0 | 3102 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | GGGCA others(3097): Show |
chr16 | 783620 | 803074 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 12 | 1 | 5 | 4 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0003 | 0/0 | 15 | 3 | 5 | 2 | 4 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0004 | 0/0 | 10 | 0 | 3 | 4 | 2 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0009t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0009t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0009t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0009t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0016t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0016t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0016t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0024t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0024t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0024t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0032t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0032t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0034t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0057t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0001c0058t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0001 | 0/0 | 40 | 0 | 2 | 33 | 2 | 3 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0039t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0040t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0075t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0078t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0002c0079t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0001g0008 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0007t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0017t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0028t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0028t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0028t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0067t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0070t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0072t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0003c0073t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0005t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0013t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0013t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0013t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0013t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0021t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0021t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0004c0048t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0005c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0006c0051t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0007c0012t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0007c0012t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0007c0012t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0007c0030t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0007c0030t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0007c0030t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0008c0008t0001g0005 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0009c0011t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0009c0011t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0009c0027t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0009c0027t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0009c0027t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0010c0010t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0010c0010t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0010c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0010c0010t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0010c0064t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0011c0020t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0011c0031t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0012c0015t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0012c0015t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0012c0015t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0012c0015t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0013c0014t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0013c0014t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0013c0014t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0014c0029t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0014c0029t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0014c0029t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0015c0025t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0015c0025t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0016c0023t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0016c0023t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0016c0023t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0017c0022t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0017c0022t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0018c0019t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0018c0019t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0018c0019t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0019c0026t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0019c0026t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0020c0018t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0020c0018t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0021c0036t0004g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0022c0035t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0022c0035t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0023c0038t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0023c0038t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0024c0042t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0024c0042t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0025c0041t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0025c0041t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0026c0037t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0027c0033t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0027c0033t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0028c0045t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0029c0055t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0030c0074t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0031c0077t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0032c0052t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0033c0066t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0034c0043t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0035c0060t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0036c0044t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0037c0069t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0038c0068t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0039c0062t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0040c0047t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0041c0046t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0042c0071t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0043c0054t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0044c0080t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0045c0049t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0046c0053t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0047c0056t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0048c0063t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0049c0061t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0050c0065t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0051c0050t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0052c0059t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
a0053c0076t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00140 | hp1 | a0001 | c0016 | t0001 | g0044 | EUR | GBR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0124 | EUR | GBR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00280 | hp2 | a0001 | c0024 | t0001 | g0002 | EUR | FIN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00323 | hp1 | a0001 | c0016 | t0001 | g0044 | EUR | FIN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00423 | hp1 | a0014 | c0029 | t0001 | g0185 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00544 | hp1 | a0003 | c0003 | t0001 | g0059 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00558 | hp2 | a0006 | c0051 | t0001 | g0081 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00639 | hp1 | a0007 | c0030 | t0002 | g0048 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00639 | hp2 | a0004 | c0005 | t0002 | g0026 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00642 | hp1 | a0006 | c0006 | t0001 | g0020 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00735 | hp1 | a0003 | c0007 | t0001 | g0008 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00735 | hp2 | a0015 | c0025 | t0001 | g0168 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00738 | hp1 | a0004 | c0005 | t0002 | g0012 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00738 | hp2 | a0005 | c0004 | t0001 | g0007 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01069 | hp1 | a0011 | c0020 | t0001 | g0021 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01069 | hp2 | a0002 | c0040 | t0001 | g0052 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01071 | hp2 | a0011 | c0020 | t0001 | g0021 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01074 | hp1 | a0004 | c0005 | t0002 | g0231 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01099 | hp2 | a0021 | c0036 | t0004 | g0032 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01106 | hp1 | a0004 | c0005 | t0002 | g0026 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01106 | hp2 | a0003 | c0007 | t0001 | g0008 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01109 | hp1 | a0004 | c0021 | t0001 | g0058 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01109 | hp2 | a0016 | c0023 | t0001 | g0169 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01167 | hp2 | a0003 | c0007 | t0001 | g0191 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01192 | hp2 | a0002 | c0040 | t0001 | g0052 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01243 | hp1 | a0028 | c0045 | t0001 | g0086 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0065 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01261 | hp2 | a0015 | c0025 | t0001 | g0045 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01346 | hp2 | a0002 | c0079 | t0001 | g0208 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01433 | hp2 | a0001 | c0024 | t0001 | g0151 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01496 | hp1 | a0015 | c0025 | t0001 | g0045 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0025 | EUR | IBS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01517 | hp1 | a0022 | c0035 | t0001 | g0002 | EUR | IBS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0209 | EUR | IBS | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01884 | hp1 | a0004 | c0013 | t0002 | g0229 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01884 | hp2 | a0017 | c0022 | t0001 | g0039 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01891 | hp1 | a0029 | c0055 | t0001 | g0113 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01891 | hp2 | a0001 | c0009 | t0001 | g0002 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01934 | hp1 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01943 | hp1 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01978 | hp1 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01981 | hp1 | a0030 | c0074 | t0001 | g0173 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01993 | hp2 | a0003 | c0003 | t0001 | g0072 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02004 | hp1 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02055 | hp1 | a0007 | c0012 | t0003 | g0054 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02055 | hp2 | a0001 | c0009 | t0001 | g0165 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02056 | hp2 | a0004 | c0005 | t0002 | g0224 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02071 | hp1 | a0031 | c0077 | t0001 | g0001 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02074 | hp1 | a0003 | c0073 | t0001 | g0069 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02080 | hp1 | a0002 | c0075 | t0001 | g0206 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02080 | hp2 | a0032 | c0052 | t0001 | g0020 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02083 | hp1 | a0014 | c0029 | t0001 | g0186 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02083 | hp2 | a0018 | c0019 | t0001 | g0094 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02148 | hp2 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | CDX | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02155 | hp2 | a0001 | c0058 | t0001 | g0002 | EAS | CDX | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CDX | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02165 | hp2 | a0018 | c0019 | t0001 | g0093 | EAS | CDX | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02257 | hp1 | a0024 | c0042 | t0001 | g0235 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02258 | hp1 | a0004 | c0005 | t0002 | g0220 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02258 | hp2 | a0005 | c0004 | t0001 | g0107 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02273 | hp1 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02280 | hp1 | a0005 | c0004 | t0001 | g0112 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02280 | hp2 | a0011 | c0031 | t0001 | g0034 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02293 | hp1 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02300 | hp2 | a0008 | c0008 | t0001 | g0005 | AMR | PEL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02451 | hp1 | a0003 | c0017 | t0001 | g0009 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02451 | hp2 | a0012 | c0015 | t0001 | g0007 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02572 | hp1 | a0012 | c0015 | t0001 | g0118 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02572 | hp2 | a0024 | c0042 | t0001 | g0236 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02602 | hp1 | a0003 | c0007 | t0001 | g0183 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02602 | hp2 | a0006 | c0006 | t0001 | g0030 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02615 | hp1 | a0005 | c0004 | t0001 | g0181 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02615 | hp2 | a0011 | c0020 | t0001 | g0021 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02622 | hp1 | a0004 | c0021 | t0001 | g0027 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02622 | hp2 | a0007 | c0030 | t0002 | g0190 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02630 | hp1 | a0001 | c0009 | t0001 | g0004 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02630 | hp2 | a0009 | c0027 | t0001 | g0090 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02647 | hp1 | a0019 | c0026 | t0001 | g0089 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02647 | hp2 | a0009 | c0011 | t0001 | g0016 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02683 | hp1 | a0016 | c0023 | t0001 | g0170 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02698 | hp2 | a0001 | c0057 | t0001 | g0010 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02717 | hp1 | a0020 | c0018 | t0001 | g0031 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02717 | hp2 | a0034 | c0043 | t0001 | g0008 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02723 | hp1 | a0003 | c0007 | t0001 | g0008 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02723 | hp2 | a0003 | c0070 | t0002 | g0048 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02735 | hp2 | a0005 | c0004 | t0001 | g0116 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02738 | hp1 | a0022 | c0035 | t0001 | g0152 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02809 | hp1 | a0035 | c0060 | t0001 | g0003 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02809 | hp2 | a0007 | c0012 | t0003 | g0054 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02818 | hp1 | a0009 | c0011 | t0001 | g0096 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02818 | hp2 | a0005 | c0004 | t0001 | g0172 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02886 | hp1 | a0019 | c0026 | t0001 | g0033 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02886 | hp2 | a0013 | c0014 | t0001 | g0175 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02895 | hp1 | a0004 | c0021 | t0001 | g0027 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02895 | hp2 | a0017 | c0022 | t0001 | g0007 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02896 | hp1 | a0007 | c0012 | t0003 | g0232 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02896 | hp2 | a0013 | c0014 | t0001 | g0043 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02897 | hp1 | a0013 | c0014 | t0001 | g0043 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02897 | hp2 | a0036 | c0044 | t0001 | g0057 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02965 | hp1 | a0009 | c0011 | t0001 | g0016 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02965 | hp2 | a0001 | c0009 | t0001 | g0002 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02970 | hp1 | a0020 | c0018 | t0001 | g0031 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02970 | hp2 | a0003 | c0007 | t0001 | g0047 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02976 | hp1 | a0017 | c0022 | t0001 | g0007 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02976 | hp2 | a0037 | c0069 | t0001 | g0053 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03017 | hp1 | a0001 | c0024 | t0001 | g0003 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03041 | hp1 | a0020 | c0018 | t0001 | g0087 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03041 | hp2 | a0001 | c0034 | t0002 | g0046 | AFR | GWD | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03098 | hp1 | a0007 | c0012 | t0003 | g0055 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03098 | hp2 | a0001 | c0034 | t0002 | g0046 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03130 | hp1 | a0009 | c0011 | t0001 | g0016 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03139 | hp1 | a0007 | c0012 | t0003 | g0055 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03139 | hp2 | a0003 | c0067 | t0001 | g0009 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03195 | hp1 | a0009 | c0027 | t0001 | g0092 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03195 | hp2 | a0003 | c0007 | t0001 | g0008 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03209 | hp1 | a0005 | c0004 | t0001 | g0177 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03209 | hp2 | a0007 | c0030 | t0002 | g0189 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03225 | hp1 | a0004 | c0013 | t0002 | g0227 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03225 | hp2 | a0003 | c0007 | t0001 | g0192 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03239 | hp2 | a0004 | c0005 | t0002 | g0012 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03453 | hp1 | a0001 | c0009 | t0001 | g0127 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03453 | hp2 | a0013 | c0014 | t0001 | g0109 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03486 | hp1 | a0004 | c0005 | t0002 | g0221 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03486 | hp2 | a0038 | c0068 | t0001 | g0053 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03491 | hp1 | a0039 | c0062 | t0001 | g0002 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03492 | hp2 | a0040 | c0047 | t0002 | g0012 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03516 | hp1 | a0011 | c0031 | t0001 | g0034 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03516 | hp2 | a0041 | c0046 | t0001 | g0230 | AFR | ESN | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03579 | hp1 | a0042 | c0071 | t0001 | g0211 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03579 | hp2 | a0004 | c0013 | t0002 | g0226 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03654 | hp1 | a0004 | c0005 | t0002 | g0012 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03669 | hp1 | a0004 | c0005 | t0002 | g0223 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03669 | hp2 | a0006 | c0006 | t0001 | g0082 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03688 | hp1 | a0005 | c0004 | t0001 | g0132 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03688 | hp2 | a0004 | c0005 | t0002 | g0222 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03704 | hp2 | a0016 | c0023 | t0001 | g0171 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03710 | hp1 | a0001 | c0016 | t0001 | g0148 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03710 | hp2 | a0043 | c0054 | t0001 | g0115 | SAS | PJL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03831 | hp1 | a0001 | c0016 | t0001 | g0160 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03831 | hp2 | a0044 | c0080 | t0001 | g0001 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03927 | hp1 | a0006 | c0006 | t0001 | g0080 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04115 | hp1 | a0005 | c0004 | t0001 | g0119 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04184 | hp1 | a0045 | c0049 | t0001 | g0084 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0215 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04204 | hp1 | a0006 | c0006 | t0001 | g0015 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04204 | hp2 | a0046 | c0053 | t0001 | g0234 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04228 | hp1 | a0006 | c0006 | t0001 | g0030 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18522 | hp1 | a0019 | c0026 | t0001 | g0033 | AFR | YRI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18522 | hp2 | a0009 | c0011 | t0001 | g0016 | AFR | YRI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18747 | hp1 | a0010 | c0010 | t0001 | g0035 | EAS | CHB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18906 | hp1 | a0005 | c0004 | t0001 | g0007 | AFR | YRI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18906 | hp2 | a0003 | c0017 | t0001 | g0009 | AFR | YRI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18939 | hp2 | a0003 | c0028 | t0001 | g0013 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18940 | hp1 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18944 | hp2 | a0047 | c0056 | t0001 | g0194 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18946 | hp1 | a0010 | c0010 | t0001 | g0105 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18946 | hp2 | a0003 | c0028 | t0001 | g0006 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18950 | hp2 | a0006 | c0006 | t0001 | g0078 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18953 | hp2 | a0026 | c0037 | t0001 | g0050 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18956 | hp1 | a0010 | c0010 | t0001 | g0104 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18956 | hp2 | a0006 | c0006 | t0001 | g0015 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18959 | hp2 | a0004 | c0048 | t0002 | g0012 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18960 | hp1 | a0002 | c0078 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18960 | hp2 | a0048 | c0063 | t0001 | g0004 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18961 | hp1 | a0049 | c0061 | t0001 | g0142 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18969 | hp1 | a0006 | c0006 | t0001 | g0015 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18974 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18974 | hp2 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18975 | hp1 | a0010 | c0010 | t0001 | g0035 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18977 | hp1 | a0003 | c0072 | t0001 | g0075 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18980 | hp1 | a0050 | c0065 | t0001 | g0002 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18980 | hp2 | a0004 | c0005 | t0002 | g0228 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18983 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18986 | hp1 | a0003 | c0007 | t0001 | g0029 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18986 | hp2 | a0006 | c0006 | t0001 | g0020 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18991 | hp1 | a0051 | c0050 | t0001 | g0079 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18999 | hp2 | a0002 | c0039 | t0001 | g0051 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19000 | hp1 | a0052 | c0059 | t0001 | g0195 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19005 | hp1 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19009 | hp1 | a0006 | c0006 | t0001 | g0015 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19012 | hp1 | a0018 | c0019 | t0001 | g0095 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19030 | hp1 | a0005 | c0004 | t0001 | g0117 | AFR | LWK | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19030 | hp2 | a0005 | c0004 | t0001 | g0138 | AFR | LWK | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19043 | hp1 | a0003 | c0017 | t0001 | g0009 | AFR | LWK | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19043 | hp2 | a0023 | c0038 | t0001 | g0233 | AFR | LWK | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19054 | hp2 | a0003 | c0028 | t0001 | g0014 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19057 | hp1 | a0006 | c0006 | t0001 | g0077 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19065 | hp1 | a0027 | c0033 | t0001 | g0099 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19067 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19074 | hp2 | a0010 | c0010 | t0001 | g0102 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19076 | hp1 | a0053 | c0076 | t0001 | g0214 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19076 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19077 | hp1 | a0002 | c0039 | t0001 | g0051 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19077 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19079 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19079 | hp2 | a0010 | c0064 | t0001 | g0103 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19080 | hp2 | a0003 | c0007 | t0006 | g0029 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19088 | hp1 | a0027 | c0033 | t0001 | g0098 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19088 | hp2 | a0006 | c0006 | t0001 | g0083 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19091 | hp2 | a0026 | c0037 | t0001 | g0050 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19240 | hp1 | a0004 | c0013 | t0002 | g0225 | AFR | YRI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA19240 | hp2 | a0003 | c0007 | t0001 | g0008 | AFR | YRI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20129 | hp1 | a0005 | c0004 | t0001 | g0108 | AFR | ASW | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20129 | hp2 | a0005 | c0004 | t0001 | g0056 | AFR | ASW | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20805 | hp1 | a0005 | c0004 | t0001 | g0163 | EUR | TSI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20905 | hp1 | a0021 | c0036 | t0004 | g0032 | SAS | GIH | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20905 | hp2 | a0004 | c0005 | t0002 | g0026 | SAS | GIH | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG01123 | hp2 | a0014 | c0029 | t0001 | g0184 | AMR | CLM | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02109 | hp1 | a0023 | c0038 | t0001 | g0212 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02109 | hp2 | a0005 | c0004 | t0001 | g0007 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02486 | hp1 | a0012 | c0015 | t0001 | g0114 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02486 | hp2 | a0033 | c0066 | t0001 | g0047 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02559 | hp1 | a0001 | c0009 | t0001 | g0004 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG02559 | hp2 | a0005 | c0004 | t0001 | g0007 | AFR | ACB | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03471 | hp1 | a0012 | c0015 | t0001 | g0039 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG03471 | hp2 | a0025 | c0041 | t0001 | g0188 | AFR | MSL | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG06807 | hp1 | a0003 | c0017 | t0001 | g0009 | AFR | USA | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA18955 | hp2 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20300 | hp1 | a0001 | c0032 | t0001 | g0122 | AFR | USA | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA20300 | hp2 | a0009 | c0027 | t0001 | g0091 | AFR | USA | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA21309 | hp1 | a0025 | c0041 | t0007 | g0187 | AFR | LWK | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
NA21309 | hp2 | a0005 | c0004 | t0001 | g0164 | AFR | LWK | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0210 | REF | REF | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
homoSapiens | grch38p0 | a0001 | c0032 | t0001 | g0162 | REF | REF | CHTF18_chr16_783620_803074 | CHTF18 | chr16 | 783620 | 803074 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:788955 | G | A | 1 | a0034 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.116G>A | p.Gly39Glu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/22 | 181/3092 | 116/2928 | 39/975 | chr16 | 788955 | |||
chr16:789027 | C | T | 4 | a0007 a0014 a0024 others(1): Show |
15 | HG00423.hp1 HG00639.hp1 HG01123.hp2 others(12): Show |
missense_variant | MODERATE | c.188C>T | p.Ser63Phe | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/22 | 253/3092 | 188/2928 | 63/975 | chr16 | 789027 | |||
chr16:789084 | A | C | 4 | a0002 a0031 a0044 others(1): Show |
69 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(66): Show |
missense_variant | MODERATE | c.245A>C | p.Gln82Pro | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/22 | 310/3092 | 245/2928 | 82/975 | chr16 | 789084 | |||
chr16:789215 | A | G | 1 | a0036 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.292A>G | p.Arg98Gly | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 357/3092 | 292/2928 | 98/975 | chr16 | 789215 | |||
chr16:789217 | G | C | 1 | a0036 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.294G>C | p.Arg98Ser | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 359/3092 | 294/2928 | 98/975 | chr16 | 789217 | |||
chr16:789224 | C | T | 1 | a0030 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.301C>T | p.Arg101Trp | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 366/3092 | 301/2928 | 101/975 | chr16 | 789224 | |||
chr16:789269 | G | A | 15 | a0004 a0006 a0011 others(12): Show |
59 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(56): Show |
missense_variant | MODERATE | c.346G>A | p.Glu116Lys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 411/3092 | 346/2928 | 116/975 | chr16 | 789269 | |||
chr16:789297 | C | T | 1 | a0046 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.374C>T | p.Ser125Phe | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 439/3092 | 374/2928 | 125/975 | chr16 | 789297 | |||
chr16:789600 | G | A | 6 | a0005 a0012 a0016 others(3): Show |
30 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(27): Show |
missense_variant | MODERATE | c.491G>A | p.Arg164His | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/22 | 556/3092 | 491/2928 | 164/975 | chr16 | 789600 | |||
chr16:789666 | T | G | 1 | a0013 | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.557T>G | p.Val186Gly | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/22 | 622/3092 | 557/2928 | 186/975 | chr16 | 789666 | |||
chr16:789702 | C | T | 1 | a0032 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.593C>T | p.Ala198Val | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/22 | 658/3092 | 593/2928 | 198/975 | chr16 | 789702 | |||
chr16:789707 | G | T | 1 | a0036 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.598G>T | p.Gly200Trp | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/22 | 663/3092 | 598/2928 | 200/975 | chr16 | 789707 | |||
chr16:790267 | G | A | 2 | a0020 a0028 |
4 | HG01243.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.697G>A | p.Glu233Lys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 5/22 | 762/3092 | 697/2928 | 233/975 | chr16 | 790267 | |||
chr16:790378 | A | G | 33 | a0002 a0003 a0004 others(30): Show |
223 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
missense_variant | MODERATE | c.731A>G | p.Lys244Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 6/22 | 796/3092 | 731/2928 | 244/975 | chr16 | 790378 | |||
chr16:790532 | T | C | 1 | a0033 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.760T>C | p.Ser254Pro | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 825/3092 | 760/2928 | 254/975 | chr16 | 790532 | |||
chr16:790544 | G | A | 1 | a0047 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.772G>A | p.Glu258Lys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 837/3092 | 772/2928 | 258/975 | chr16 | 790544 | |||
chr16:790569 | C | T | 1 | a0022 | 2 | HG01517.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.797C>T | p.Pro266Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 862/3092 | 797/2928 | 266/975 | chr16 | 790569 | |||
chr16:790599 | C | T | 6 | a0004 a0014 a0025 others(3): Show |
29 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(26): Show |
missense_variant | MODERATE | c.827C>T | p.Ala276Val | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 892/3092 | 827/2928 | 276/975 | chr16 | 790599 | |||
chr16:790607 | C | G | 1 | a0019 | 3 | HG02647.hp1 HG02886.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.835C>G | p.His279Asp | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 900/3092 | 835/2928 | 279/975 | chr16 | 790607 | |||
chr16:790624 | T | A | 1 | a0017 | 3 | HG01884.hp2 HG02895.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.852T>A | p.Asp284Glu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 917/3092 | 852/2928 | 284/975 | chr16 | 790624 | |||
chr16:791909 | C | T | 1 | a0042 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1163C>T | p.Ala388Val | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 9/22 | 1228/3092 | 1163/2928 | 388/975 | chr16 | 791909 | |||
chr16:792249 | C | T | 1 | a0024 | 2 | HG02257.hp1 HG02572.hp2 |
missense_variant | MODERATE | c.1228C>T | p.Arg410Cys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 10/22 | 1293/3092 | 1228/2928 | 410/975 | chr16 | 792249 | |||
chr16:792508 | G | T | 1 | a0012 | 4 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.1396G>T | p.Ala466Ser | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/22 | 1461/3092 | 1396/2928 | 466/975 | chr16 | 792508 | |||
chr16:792518 | C | T | 1 | a0021 | 2 | HG01099.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.1406C>T | p.Ser469Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/22 | 1471/3092 | 1406/2928 | 469/975 | chr16 | 792518 | |||
chr16:792800 | C | G | 1 | a0019 | 3 | HG02647.hp1 HG02886.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1561C>G | p.Arg521Gly | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 12/22 | 1626/3092 | 1561/2928 | 521/975 | chr16 | 792800 | |||
chr16:794059 | G | A | 3 | a0037 a0038 a0041 |
3 | HG02976.hp2 HG03486.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.1808G>A | p.Arg603His | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/22 | 1873/3092 | 1808/2928 | 603/975 | chr16 | 794059 | |||
chr16:794064 | G | A | 1 | a0052 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.1813G>A | p.Gly605Ser | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/22 | 1878/3092 | 1813/2928 | 605/975 | chr16 | 794064 | |||
chr16:794066 | C | CCAGGACC others(3): Show |
1 | a0053 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1817_1826dupAGGACC others(4): Show |
p.Leu610fs | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/22 | 1892/3092 | 1827/2928 | 609/975 | INFO_REALIGN_3_PRIME | chr16 | 794066 | ||
chr16:794070 | G | A | 1 | a0035 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1819G>A | p.Asp607Asn | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/22 | 1884/3092 | 1819/2928 | 607/975 | chr16 | 794070 | |||
chr16:795725 | C | T | 1 | a0050 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.2216C>T | p.Thr739Met | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2281/3092 | 2216/2928 | 739/975 | chr16 | 795725 | |||
chr16:795730 | G | T | 1 | a0010 | 6 | NA18747.hp1 NA18946.hp1 NA18956.hp1 others(3): Show |
missense_variant | MODERATE | c.2221G>T | p.Val741Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2286/3092 | 2221/2928 | 741/975 | chr16 | 795730 | |||
chr16:795742 | G | A | 4 | a0006 a0032 a0045 others(1): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
missense_variant | MODERATE | c.2233G>A | p.Ala745Thr | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2298/3092 | 2233/2928 | 745/975 | chr16 | 795742 | |||
chr16:795754 | C | T | 1 | a0008 | 8 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(5): Show |
missense_variant | MODERATE | c.2245C>T | p.Arg749Cys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2310/3092 | 2245/2928 | 749/975 | chr16 | 795754 | |||
chr16:795797 | G | C | 5 | a0008 a0009 a0037 others(2): Show |
19 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(16): Show |
missense_variant | MODERATE | c.2288G>C | p.Cys763Ser | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2353/3092 | 2288/2928 | 763/975 | chr16 | 795797 | |||
chr16:795832 | C | T | 1 | a0040 | 1 | HG03492.hp2 | missense_variant&splice_region_variant | MODERATE | c.2323C>T | p.Pro775Ser | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2388/3092 | 2323/2928 | 775/975 | chr16 | 795832 | |||
chr16:796005 | C | T | 2 | a0037 a0041 |
2 | HG02976.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.2384C>T | p.Thr795Met | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/22 | 2449/3092 | 2384/2928 | 795/975 | chr16 | 796005 | |||
chr16:796031 | C | T | 3 | a0011 a0023 a0042 |
8 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
missense_variant | MODERATE | c.2410C>T | p.Arg804Cys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/22 | 2475/3092 | 2410/2928 | 804/975 | chr16 | 796031 | |||
chr16:796721 | G | A | 1 | a0043 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2461G>A | p.Val821Met | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/22 | 2526/3092 | 2461/2928 | 821/975 | chr16 | 796721 | |||
chr16:796797 | G | T | 1 | a0029 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2537G>T | p.Arg846Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/22 | 2602/3092 | 2537/2928 | 846/975 | chr16 | 796797 | |||
chr16:796811 | G | C | 1 | a0027 | 2 | NA19065.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.2551G>C | p.Glu851Gln | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/22 | 2616/3092 | 2551/2928 | 851/975 | chr16 | 796811 | |||
chr16:797004 | T | C | 1 | a0049 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.2645T>C | p.Ile882Thr | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2710/3092 | 2645/2928 | 882/975 | chr16 | 797004 | |||
chr16:797009 | G | A | 1 | a0045 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.2650G>A | p.Glu884Lys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2715/3092 | 2650/2928 | 884/975 | chr16 | 797009 | |||
chr16:797033 | C | G | 1 | a0020 | 3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.2674C>G | p.Pro892Ala | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2739/3092 | 2674/2928 | 892/975 | chr16 | 797033 | |||
chr16:797043 | A | G | 1 | a0044 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2684A>G | p.His895Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2749/3092 | 2684/2928 | 895/975 | chr16 | 797043 | |||
chr16:797075 | G | A | 1 | a0025 | 2 | HG03471.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.2716G>A | p.Ala906Thr | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2781/3092 | 2716/2928 | 906/975 | chr16 | 797075 | |||
chr16:797743 | C | T | 6 | a0002 a0015 a0016 others(3): Show |
76 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
missense_variant | MODERATE | c.2783C>T | p.Pro928Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 21/22 | 2848/3092 | 2783/2928 | 928/975 | chr16 | 797743 | |||
chr16:797748 | G | A | 1 | a0039 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.2788G>A | p.Ala930Thr | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 21/22 | 2853/3092 | 2788/2928 | 930/975 | chr16 | 797748 | |||
chr16:797845 | C | T | 1 | a0051 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.2798C>T | p.Thr933Met | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 2863/3092 | 2798/2928 | 933/975 | chr16 | 797845 | |||
chr16:797877 | A | G | 1 | a0048 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.2830A>G | p.Met944Val | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 2895/3092 | 2830/2928 | 944/975 | chr16 | 797877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:788705 | G | A | 1 | a0011c0031 | 2 | HG02280.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.21G>A | p.Glu7Glu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/22 | 86/3092 | 21/2928 | 7/975 | chr16 | 788705 | |||
chr16:789214 | C | A | 1 | a0036c0044 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.291C>A | p.Pro97Pro | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 356/3092 | 291/2928 | 97/975 | chr16 | 789214 | |||
chr16:789262 | A | G | 79 | a0001c0001 a0001c0009 a0001c0016 others(76): Show |
425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
synonymous_variant | LOW | c.339A>G | p.Arg113Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 404/3092 | 339/2928 | 113/975 | chr16 | 789262 | |||
chr16:789304 | G | A | 1 | a0013c0014 | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.381G>A | p.Pro127Pro | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/22 | 446/3092 | 381/2928 | 127/975 | chr16 | 789304 | |||
chr16:789646 | C | T | 1 | a0001c0009 | 6 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
synonymous_variant | LOW | c.537C>T | p.His179His | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/22 | 602/3092 | 537/2928 | 179/975 | chr16 | 789646 | |||
chr16:789658 | G | A | 1 | a0002c0075 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.549G>A | p.Thr183Thr | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/22 | 614/3092 | 549/2928 | 183/975 | chr16 | 789658 | |||
chr16:790191 | C | T | 1 | a0044c0080 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.621C>T | p.His207His | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 5/22 | 686/3092 | 621/2928 | 207/975 | chr16 | 790191 | |||
chr16:790531 | G | A | 1 | a0019c0026 | 3 | HG02647.hp1 HG02886.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.759G>A | p.Arg253Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 824/3092 | 759/2928 | 253/975 | chr16 | 790531 | |||
chr16:790579 | G | A | 1 | a0001c0057 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.807G>A | p.Glu269Glu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 872/3092 | 807/2928 | 269/975 | chr16 | 790579 | |||
chr16:790597 | C | T | 10 | a0003c0003 a0003c0028 a0003c0072 others(7): Show |
56 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(53): Show |
synonymous_variant | LOW | c.825C>T | p.Asp275Asp | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 890/3092 | 825/2928 | 275/975 | chr16 | 790597 | |||
chr16:790636 | C | G | 1 | a0002c0040 | 2 | HG01069.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.864C>G | p.Pro288Pro | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 929/3092 | 864/2928 | 288/975 | chr16 | 790636 | |||
chr16:790645 | C | T | 1 | a0002c0079 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.873C>T | p.Tyr291Tyr | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/22 | 938/3092 | 873/2928 | 291/975 | chr16 | 790645 | |||
chr16:791175 | C | T | 6 | a0003c0017 a0004c0005 a0004c0013 others(3): Show |
24 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(21): Show |
synonymous_variant | LOW | c.909C>T | p.Cys303Cys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/22 | 974/3092 | 909/2928 | 303/975 | chr16 | 791175 | |||
chr16:791238 | G | A | 1 | a0001c0016 | 4 | HG00140.hp1 HG00323.hp1 HG03710.hp1 others(1): Show |
synonymous_variant | LOW | c.972G>A | p.Lys324Lys | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/22 | 1037/3092 | 972/2928 | 324/975 | chr16 | 791238 | |||
chr16:792288 | C | T | 3 | a0002c0039 a0008c0008 a0009c0011 |
15 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(12): Show |
synonymous_variant | LOW | c.1267C>T | p.Leu423Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 10/22 | 1332/3092 | 1267/2928 | 423/975 | chr16 | 792288 | |||
chr16:792299 | C | T | 1 | a0003c0073 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1278C>T | p.Gly426Gly | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 10/22 | 1343/3092 | 1278/2928 | 426/975 | chr16 | 792299 | |||
chr16:792450 | C | T | 11 | a0002c0002 a0002c0040 a0002c0075 others(8): Show |
72 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(69): Show |
synonymous_variant | LOW | c.1338C>T | p.Asn446Asn | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/22 | 1403/3092 | 1338/2928 | 446/975 | chr16 | 792450 | |||
chr16:793016 | C | A | 2 | a0003c0017 a0003c0067 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
synonymous_variant | LOW | c.1623C>A | p.Leu541Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/22 | 1688/3092 | 1623/2928 | 541/975 | chr16 | 793016 | |||
chr16:793022 | G | A | 1 | a0001c0058 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1629G>A | p.Glu543Glu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/22 | 1694/3092 | 1629/2928 | 543/975 | chr16 | 793022 | |||
chr16:793200 | C | T | 1 | a0001c0034 | 2 | HG03041.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1728C>T | p.Arg576Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/22 | 1793/3092 | 1728/2928 | 576/975 | chr16 | 793200 | |||
chr16:795248 | C | T | 1 | a0002c0040 | 2 | HG01069.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.2067C>T | p.Ser689Ser | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/22 | 2132/3092 | 2067/2928 | 689/975 | chr16 | 795248 | |||
chr16:795278 | C | T | 1 | a0021c0036 | 2 | HG01099.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.2097C>T | p.Pro699Pro | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/22 | 2162/3092 | 2097/2928 | 699/975 | chr16 | 795278 | |||
chr16:795819 | A | G | 21 | a0001c0034 a0003c0070 a0004c0005 others(18): Show |
63 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(60): Show |
synonymous_variant | LOW | c.2310A>G | p.Ala770Ala | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2375/3092 | 2310/2928 | 770/975 | chr16 | 795819 | |||
chr16:795828 | C | G | 1 | a0004c0048 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.2319C>G | p.Leu773Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/22 | 2384/3092 | 2319/2928 | 773/975 | chr16 | 795828 | |||
chr16:796012 | C | T | 1 | a0007c0012 | 5 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.2391C>T | p.Leu797Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/22 | 2456/3092 | 2391/2928 | 797/975 | chr16 | 796012 | |||
chr16:796022 | C | T | 1 | a0006c0051 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.2401C>T | p.Leu801Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/22 | 2466/3092 | 2401/2928 | 801/975 | chr16 | 796022 | |||
chr16:796720 | C | T | 1 | a0028c0045 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2460C>T | p.Asn820Asn | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/22 | 2525/3092 | 2460/2928 | 820/975 | chr16 | 796720 | |||
chr16:796798 | C | T | 2 | a0008c0008 a0009c0011 |
13 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(10): Show |
synonymous_variant | LOW | c.2538C>T | p.Arg846Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/22 | 2603/3092 | 2538/2928 | 846/975 | chr16 | 796798 | |||
chr16:796804 | C | T | 6 | a0006c0006 a0006c0051 a0032c0052 others(3): Show |
18 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(15): Show |
synonymous_variant | LOW | c.2544C>T | p.Ile848Ile | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/22 | 2609/3092 | 2544/2928 | 848/975 | chr16 | 796804 | |||
chr16:796996 | G | A | 1 | a0003c0072 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.2637G>A | p.Leu879Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2702/3092 | 2637/2928 | 879/975 | chr16 | 796996 | |||
chr16:796999 | G | A | 1 | a0001c0024 | 3 | HG00280.hp2 HG01433.hp2 HG03017.hp1 |
synonymous_variant | LOW | c.2640G>A | p.Gly880Gly | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2705/3092 | 2640/2928 | 880/975 | chr16 | 796999 | |||
chr16:797074 | A | G | 1 | a0002c0078 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.2715A>G | p.Arg905Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2780/3092 | 2715/2928 | 905/975 | chr16 | 797074 | |||
chr16:797083 | G | A | 1 | a0003c0028 | 3 | NA18939.hp2 NA18946.hp2 NA19054.hp2 |
synonymous_variant | LOW | c.2724G>A | p.Arg908Arg | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/22 | 2789/3092 | 2724/2928 | 908/975 | chr16 | 797083 | |||
chr16:797936 | C | T | 4 | a0004c0005 a0004c0048 a0019c0026 others(1): Show |
18 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(15): Show |
synonymous_variant | LOW | c.2889C>T | p.Asn963Asn | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 2954/3092 | 2889/2928 | 963/975 | chr16 | 797936 | |||
chr16:797954 | G | A | 1 | a0010c0064 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.2907G>A | p.Leu969Leu | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 2972/3092 | 2907/2928 | 969/975 | chr16 | 797954 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:788637 | G | T | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/22 | chr16 | 788637 | |||||||
chr16:788648 | G | A | 1 | a0001c0001t0005 | 1 | HG00140.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/22 | 37 | chr16 | 788648 | ||||||
chr16:797986 | C | T | 1 | a0007c0012t0003 | 5 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 11 | chr16 | 797986 | ||||||
chr16:797988 | C | T | 1 | a0025c0041t0007 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 13 | chr16 | 797988 | ||||||
chr16:798000 | C | T | 1 | a0021c0036t0004 | 2 | HG01099.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*25C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 25 | chr16 | 798000 | ||||||
chr16:798002 | C | T | 1 | a0003c0007t0006 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 27 | chr16 | 798002 | ||||||
chr16:798013 | G | A | 7 | a0001c0034t0002 a0003c0070t0002 a0004c0005t0002 others(4): Show |
25 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 22/22 | 38 | chr16 | 798013 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:788816 | G | A | 1 | a0005c0004t0001g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+41G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/21 | chr16 | 788816 | |||||||
chr16:788825 | G | A | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+50G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/21 | chr16 | 788825 | |||||||
chr16:788852 | G | A | 1 | a0003c0003t0001g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.91+77G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/21 | chr16 | 788852 | |||||||
chr16:788888 | C | T | 1 | a0002c0002t0001g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.92-43C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 1/21 | chr16 | 788888 | |||||||
chr16:789147 | A | G | 2 | a0024c0042t0001g0235 a0024c0042t0001g0236 |
2 | HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.286+22A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/21 | chr16 | 789147 | |||||||
chr16:789158 | A | G | 1 | a0046c0053t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+33A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/21 | chr16 | 789158 | |||||||
chr16:789166 | C | T | 1 | a0023c0038t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.286+41C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/21 | chr16 | 789166 | |||||||
chr16:789184 | T | C | 42 | a0001c0001t0001g0085 a0003c0003t0001g0006 a0003c0003t0001g0013 others(39): Show |
59 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.287-26T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 2/21 | chr16 | 789184 | |||||||
chr16:789394 | C | T | 3 | a0007c0012t0003g0054 a0007c0012t0003g0055 a0007c0012t0003g0232 |
5 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+34C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/21 | chr16 | 789394 | |||||||
chr16:789400 | A | C | 1 | a0004c0005t0002g0231 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.437+40A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/21 | chr16 | 789400 | |||||||
chr16:789429 | C | G | 16 | a0004c0005t0002g0012 a0004c0005t0002g0026 a0004c0005t0002g0220 others(13): Show |
20 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.437+69C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/21 | chr16 | 789429 | |||||||
chr16:789431 | C | A | 1 | a0028c0045t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.437+71C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/21 | chr16 | 789431 | |||||||
chr16:789455 | A | G | 3 | a0001c0001t0001g0219 a0004c0013t0002g0229 a0041c0046t0001g0230 |
3 | HG01261.hp1 HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.438-92A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/21 | chr16 | 789455 | |||||||
chr16:789480 | C | T | 2 | a0037c0069t0001g0053 a0038c0068t0001g0053 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.438-67C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 3/21 | chr16 | 789480 | |||||||
chr16:789821 | G | C | 3 | a0020c0018t0001g0031 a0020c0018t0001g0087 a0028c0045t0001g0086 |
4 | HG01243.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+106G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789821 | |||||||
chr16:789824 | C | T | 43 | a0001c0001t0001g0085 a0001c0001t0001g0218 a0003c0003t0001g0006 others(40): Show |
60 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.606+109C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789824 | |||||||
chr16:789838 | A | C | 27 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(24): Show |
74 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.606+123A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789838 | |||||||
chr16:789843 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.606+128G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789843 | |||||||
chr16:789866 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0049 others(6): Show |
16 | HG02027.hp2 NA18952.hp2 NA18954.hp2 others(13): Show |
intron_variant | MODIFIER | c.606+151C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789866 | |||||||
chr16:789881 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0193 a0047c0056t0001g0194 |
5 | HG00609.hp2 NA18944.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.606+166C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789881 | |||||||
chr16:789935 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.606+220C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789935 | |||||||
chr16:789949 | C | CT | 111 | a0001c0001t0001g0085 a0002c0002t0001g0001 a0002c0002t0001g0018 others(108): Show |
187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.607-227dupT | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 789949 | ||||||
chr16:789963 | C | G | 1 | a0003c0007t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.607-214C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789963 | |||||||
chr16:789967 | C | T | 4 | a0001c0001t0001g0182 a0004c0021t0001g0027 a0004c0021t0001g0058 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-210C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789967 | |||||||
chr16:789970 | C | T | 2 | a0002c0040t0001g0052 a0005c0004t0001g0181 |
3 | HG01069.hp2 HG01192.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.607-207C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789970 | |||||||
chr16:789993 | A | G | 17 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(14): Show |
23 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.607-184A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789993 | |||||||
chr16:789996 | T | C | 128 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(125): Show |
222 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.607-181T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 789996 | |||||||
chr16:790012 | C | T | 15 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(12): Show |
21 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-165C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 790012 | |||||||
chr16:790014 | A | C | 26 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(23): Show |
73 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.607-163A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 790014 | |||||||
chr16:790090 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.607-87A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 790090 | |||||||
chr16:790136 | C | T | 2 | a0004c0005t0002g0026 a0004c0005t0002g0231 |
4 | HG00639.hp2 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-41C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 4/21 | chr16 | 790136 | |||||||
chr16:790302 | C | G | 1 | a0002c0002t0001g0216 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.699+33C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 5/21 | chr16 | 790302 | |||||||
chr16:790307 | C | A | 41 | a0001c0001t0001g0085 a0003c0003t0001g0006 a0003c0003t0001g0013 others(38): Show |
58 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.699+38C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 5/21 | chr16 | 790307 | |||||||
chr16:790309 | G | A | 1 | a0019c0026t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700-38G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 5/21 | chr16 | 790309 | |||||||
chr16:790409 | T | C | 28 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(25): Show |
76 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.752+10T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 6/21 | chr16 | 790409 | |||||||
chr16:790486 | C | T | 15 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(12): Show |
21 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.753-39C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 6/21 | chr16 | 790486 | |||||||
chr16:790702 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.894+36C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790702 | |||||||
chr16:790730 | G | A | 5 | a0014c0029t0001g0184 a0014c0029t0001g0185 a0014c0029t0001g0186 others(2): Show |
5 | HG00423.hp1 HG01123.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.894+64G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790730 | |||||||
chr16:790752 | A | G | 1 | a0003c0007t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.894+86A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790752 | |||||||
chr16:790769 | A | G | 28 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(25): Show |
76 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.894+103A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790769 | |||||||
chr16:790772 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.894+106C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790772 | |||||||
chr16:790861 | A | C | 1 | a0005c0004t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.894+195A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790861 | |||||||
chr16:790904 | C | T | 1 | a0028c0045t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.894+238C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790904 | |||||||
chr16:790939 | C | T | 2 | a0009c0011t0001g0016 a0009c0011t0001g0096 |
5 | HG02647.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-222C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 790939 | |||||||
chr16:791014 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.895-147C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 791014 | |||||||
chr16:791036 | C | T | 1 | a0004c0005t0002g0228 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.895-125C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 791036 | |||||||
chr16:791107 | C | T | 1 | a0004c0013t0002g0227 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.895-54C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 791107 | |||||||
chr16:791122 | T | C | 1 | a0014c0029t0001g0184 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.895-39T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 7/21 | chr16 | 791122 | |||||||
chr16:791477 | G | A | 1 | a0001c0001t0008g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1104+107G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791477 | |||||||
chr16:791511 | G | A | 1 | a0002c0040t0001g0052 | 2 | HG01069.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1104+141G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791511 | |||||||
chr16:791518 | C | T | 1 | a0004c0013t0002g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1104+148C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791518 | |||||||
chr16:791530 | A | G | 1 | a0003c0007t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1104+160A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791530 | |||||||
chr16:791540 | C | G | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1104+170C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791540 | |||||||
chr16:791541 | G | A | 2 | a0027c0033t0001g0098 a0027c0033t0001g0099 |
2 | NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1104+171G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791541 | |||||||
chr16:791551 | G | A | 5 | a0014c0029t0001g0184 a0014c0029t0001g0185 a0014c0029t0001g0186 others(2): Show |
5 | HG00423.hp1 HG01123.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1104+181G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791551 | |||||||
chr16:791556 | C | A | 1 | a0026c0037t0001g0050 | 2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1104+186C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791556 | |||||||
chr16:791610 | C | T | 2 | a0037c0069t0001g0053 a0038c0068t0001g0053 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1104+240C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791610 | |||||||
chr16:791617 | C | T | 16 | a0004c0005t0002g0012 a0004c0005t0002g0026 a0004c0005t0002g0220 others(13): Show |
20 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1105-234C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791617 | |||||||
chr16:791618 | C | T | 4 | a0003c0007t0001g0183 a0018c0019t0001g0093 a0018c0019t0001g0094 others(1): Show |
4 | HG02083.hp2 HG02165.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-233C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791618 | |||||||
chr16:791625 | A | G | 28 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(25): Show |
75 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1105-226A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791625 | |||||||
chr16:791642 | T | C | 2 | a0020c0018t0001g0031 a0020c0018t0001g0087 |
3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1105-209T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791642 | |||||||
chr16:791642 | T | TTTGTCTG others(7): Show |
1 | a0001c0001t0001g0219 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1105-206_1105-193d others(16): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 791642 | ||||||
chr16:791682 | C | T | 1 | a0002c0002t0001g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1105-169C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791682 | |||||||
chr16:791710 | C | G | 102 | a0001c0001t0001g0218 a0002c0002t0001g0001 a0002c0002t0001g0018 others(99): Show |
184 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1105-141C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791710 | |||||||
chr16:791720 | C | T | 3 | a0008c0008t0001g0005 a0009c0011t0001g0016 a0009c0011t0001g0096 |
13 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1105-131C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791720 | |||||||
chr16:791754 | C | T | 1 | a0013c0014t0001g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1105-97C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791754 | |||||||
chr16:791756 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1105-95C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791756 | |||||||
chr16:791796 | C | T | 18 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(15): Show |
24 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1105-55C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791796 | |||||||
chr16:791802 | C | T | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1105-49C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791802 | |||||||
chr16:791816 | G | A | 2 | a0006c0006t0001g0077 a0006c0006t0001g0078 |
2 | NA18950.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1105-35G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 8/21 | chr16 | 791816 | |||||||
chr16:791966 | C | T | 26 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(23): Show |
72 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1202+18C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 9/21 | chr16 | 791966 | |||||||
chr16:792023 | C | G | 1 | a0053c0076t0001g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1202+75C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 9/21 | chr16 | 792023 | |||||||
chr16:792024 | G | C | 1 | a0053c0076t0001g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1202+76G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 9/21 | chr16 | 792024 | |||||||
chr16:792157 | C | T | 1 | a0003c0003t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1203-67C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 9/21 | chr16 | 792157 | |||||||
chr16:792376 | G | T | 1 | a0030c0074t0001g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1326+29G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 10/21 | chr16 | 792376 | |||||||
chr16:792382 | G | A | 14 | a0001c0001t0001g0100 a0006c0006t0001g0015 a0006c0006t0001g0020 others(11): Show |
19 | HG00558.hp2 HG00642.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1326+35G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 10/21 | chr16 | 792382 | |||||||
chr16:792394 | G | A | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-45G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 10/21 | chr16 | 792394 | |||||||
chr16:792605 | G | A | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1478+15G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/21 | chr16 | 792605 | |||||||
chr16:792655 | C | T | 1 | a0005c0004t0001g0172 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1479-63C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/21 | chr16 | 792655 | |||||||
chr16:792686 | C | T | 26 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(23): Show |
72 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1479-32C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/21 | chr16 | 792686 | |||||||
chr16:792691 | G | A | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479-27G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/21 | chr16 | 792691 | |||||||
chr16:792705 | C | T | 15 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(12): Show |
21 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1479-13C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/21 | chr16 | 792705 | |||||||
chr16:792706 | G | A | 56 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(53): Show |
113 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1479-12G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 11/21 | chr16 | 792706 | |||||||
chr16:792826 | A | G | 31 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(28): Show |
78 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1572+15A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 12/21 | chr16 | 792826 | |||||||
chr16:792875 | C | T | 2 | a0020c0018t0001g0031 a0020c0018t0001g0087 |
3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1572+64C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 12/21 | chr16 | 792875 | |||||||
chr16:792889 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1573-77C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 12/21 | chr16 | 792889 | |||||||
chr16:792921 | G | C | 2 | a0001c0001t0001g0010 a0001c0057t0001g0010 |
5 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1573-45G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 12/21 | chr16 | 792921 | |||||||
chr16:792952 | C | T | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1573-14C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 12/21 | chr16 | 792952 | |||||||
chr16:793067 | G | A | 3 | a0014c0029t0001g0184 a0014c0029t0001g0185 a0014c0029t0001g0186 |
3 | HG00423.hp1 HG01123.hp2 HG02083.hp1 |
splice_region_variant&intron_variant | LOW | c.1671+3G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/21 | chr16 | 793067 | |||||||
chr16:793076 | G | A | 2 | a0007c0030t0002g0189 a0007c0030t0002g0190 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1671+12G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/21 | chr16 | 793076 | |||||||
chr16:793084 | C | CGGGTG | 30 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(27): Show |
76 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1671+35_1671+39dup others(5): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr16 | 793084 | ||||||
chr16:793085 | G | A | 2 | a0002c0039t0001g0051 a0008c0008t0001g0005 |
10 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1671+21G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/21 | chr16 | 793085 | |||||||
chr16:793115 | C | T | 1 | a0004c0013t0002g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1672-29C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/21 | chr16 | 793115 | |||||||
chr16:793124 | T | C | 6 | a0001c0001t0001g0101 a0010c0010t0001g0035 a0010c0010t0001g0102 others(3): Show |
7 | NA18747.hp1 NA18946.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-20T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 13/21 | chr16 | 793124 | |||||||
chr16:793318 | G | A | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1802+44G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793318 | |||||||
chr16:793321 | C | T | 1 | a0006c0006t0001g0083 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1802+47C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793321 | |||||||
chr16:793370 | G | C | 3 | a0014c0029t0001g0184 a0014c0029t0001g0185 a0014c0029t0001g0186 |
3 | HG00423.hp1 HG01123.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1802+96G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793370 | |||||||
chr16:793390 | C | T | 29 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(26): Show |
75 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1802+116C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793390 | |||||||
chr16:793425 | C | A | 1 | a0016c0023t0001g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1802+151C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793425 | |||||||
chr16:793437 | T | G | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1802+163T>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793437 | |||||||
chr16:793445 | G | A | 29 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(26): Show |
75 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1802+171G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793445 | |||||||
chr16:793453 | A | C | 1 | a0005c0004t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1802+179A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793453 | |||||||
chr16:793482 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1802+208C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793482 | |||||||
chr16:793538 | C | T | 1 | a0005c0004t0001g0172 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1802+264C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793538 | |||||||
chr16:793657 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1802+383G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793657 | |||||||
chr16:793718 | C | T | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1803-336C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793718 | |||||||
chr16:793745 | C | T | 5 | a0011c0020t0001g0021 a0011c0031t0001g0034 a0018c0019t0001g0093 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1803-309C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793745 | |||||||
chr16:793894 | T | G | 1 | a0004c0005t0002g0220 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1803-160T>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793894 | |||||||
chr16:793949 | A | C | 1 | a0003c0007t0001g0191 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1803-105A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793949 | |||||||
chr16:793961 | G | C | 8 | a0011c0020t0001g0021 a0011c0031t0001g0034 a0018c0019t0001g0093 others(5): Show |
11 | HG01069.hp1 HG01071.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1803-93G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793961 | |||||||
chr16:793961 | G | T | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1803-93G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793961 | |||||||
chr16:793986 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1803-68C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 793986 | |||||||
chr16:794037 | C | T | 1 | a0021c0036t0004g0032 | 2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1803-17C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 14/21 | chr16 | 794037 | |||||||
chr16:794324 | G | C | 1 | a0002c0002t0001g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1950+123G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794324 | |||||||
chr16:794389 | C | T | 2 | a0003c0017t0001g0009 a0003c0067t0001g0009 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+188C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794389 | |||||||
chr16:794497 | G | A | 2 | a0020c0018t0001g0031 a0020c0018t0001g0087 |
3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1950+296G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794497 | |||||||
chr16:794518 | C | T | 2 | a0003c0017t0001g0009 a0003c0067t0001g0009 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+317C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794518 | |||||||
chr16:794542 | G | A | 4 | a0019c0026t0001g0033 a0019c0026t0001g0089 a0020c0018t0001g0031 others(1): Show |
6 | HG02647.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+341G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794542 | |||||||
chr16:794548 | C | T | 1 | a0016c0023t0001g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1950+347C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794548 | |||||||
chr16:794556 | G | A | 1 | a0004c0013t0002g0229 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+355G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794556 | |||||||
chr16:794594 | G | T | 3 | a0009c0011t0001g0016 a0009c0011t0001g0096 a0014c0029t0001g0186 |
6 | HG02083.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+393G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794594 | |||||||
chr16:794599 | A | T | 2 | a0021c0036t0004g0032 a0023c0038t0001g0233 |
3 | HG01099.hp2 NA19043.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1950+398A>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794599 | |||||||
chr16:794605 | C | T | 104 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(101): Show |
188 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1950+404C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794605 | |||||||
chr16:794618 | T | C | 1 | a0004c0005t0002g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1950+417T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794618 | |||||||
chr16:794619 | G | C | 1 | a0023c0038t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1950+418G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794619 | |||||||
chr16:794643 | A | G | 1 | a0010c0010t0001g0105 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1950+442A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794643 | |||||||
chr16:794685 | G | A | 2 | a0005c0004t0001g0107 a0005c0004t0001g0108 |
2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1951-447G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794685 | |||||||
chr16:794689 | T | C | 28 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(25): Show |
76 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1951-443T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794689 | |||||||
chr16:794840 | T | G | 1 | a0008c0008t0001g0005 | 8 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1951-292T>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794840 | |||||||
chr16:794857 | CTCGTGTC others(8): Show |
C | 1 | a0007c0012t0003g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1951-272_1951-258d others(17): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr16 | 794857 | ||||||
chr16:794860 | G | C | 1 | a0001c0001t0001g0024 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1951-272G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794860 | |||||||
chr16:794861 | TGTCAGTC others(8): Show |
T | 30 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(27): Show |
43 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1951-254_1951-240d others(17): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr16 | 794861 | ||||||
chr16:794876 | A | T | 1 | a0007c0012t0003g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1951-256A>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794876 | |||||||
chr16:794883 | C | T | 1 | a0025c0041t0001g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1951-249C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794883 | |||||||
chr16:794913 | G | A | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-219G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794913 | |||||||
chr16:794978 | C | T | 1 | a0004c0005t0002g0224 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1951-154C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794978 | |||||||
chr16:794983 | C | T | 1 | a0004c0005t0002g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1951-149C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 794983 | |||||||
chr16:795008 | C | T | 1 | a0045c0049t0001g0084 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1951-124C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 795008 | |||||||
chr16:795019 | C | T | 104 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(101): Show |
188 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1951-113C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 795019 | |||||||
chr16:795044 | G | C | 1 | a0013c0014t0001g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1951-88G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 795044 | |||||||
chr16:795051 | C | T | 1 | a0001c0009t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1951-81C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 795051 | |||||||
chr16:795051 | CTG | C | 11 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(8): Show |
17 | HG00735.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1951-78_1951-77del others(2): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr16 | 795051 | ||||||
chr16:795091 | C | T | 2 | a0020c0018t0001g0031 a0020c0018t0001g0087 |
3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1951-41C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 15/21 | chr16 | 795091 | |||||||
chr16:795385 | C | T | 1 | a0024c0042t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2175+29C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795385 | |||||||
chr16:795387 | C | T | 1 | a0005c0004t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2175+31C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795387 | |||||||
chr16:795400 | G | C | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+44G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795400 | |||||||
chr16:795400 | G | GCCCTCCC others(36): Show |
1 | a0009c0027t0001g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2175+47_2175+48ins others(43): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795400 | ||||||
chr16:795404 | C | T | 23 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(20): Show |
40 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.2175+48C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795404 | |||||||
chr16:795407 | T | A | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+51T>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795407 | |||||||
chr16:795407 | T | C | 26 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0001g0180 others(23): Show |
43 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175+51T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795407 | |||||||
chr16:795408 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0001g0180 |
3 | NA18959.hp1 NA18997.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2175+52G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795408 | |||||||
chr16:795409 | T | C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0001g0180 others(3): Show |
6 | HG02083.hp2 HG02165.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175+53T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795409 | |||||||
chr16:795410 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0001g0180 |
3 | NA18959.hp1 NA18997.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2175+54G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795410 | |||||||
chr16:795416 | C | T | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+60C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795416 | |||||||
chr16:795430 | CG | C | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+76delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795430 | ||||||
chr16:795432 | G | T | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+76G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795432 | |||||||
chr16:795437 | G | A | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+81G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795437 | |||||||
chr16:795439 | G | GC | 11 | a0003c0007t0001g0047 a0006c0051t0001g0081 a0007c0012t0003g0055 others(8): Show |
15 | HG00558.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.2175+86dupC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795439 | ||||||
chr16:795439 | G | GCC | 3 | a0006c0006t0001g0015 a0006c0006t0001g0083 a0007c0012t0003g0054 |
7 | HG02055.hp1 HG02809.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.2175+85_2175+86dup others(2): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795439 | ||||||
chr16:795439 | G | GCCC | 8 | a0006c0006t0001g0020 a0006c0006t0001g0030 a0006c0006t0001g0077 others(5): Show |
10 | HG00642.hp1 HG02080.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175+84_2175+86dup others(3): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795439 | ||||||
chr16:795439 | GC | G | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+86delC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795439 | ||||||
chr16:795443 | G | C | 26 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0192 others(23): Show |
36 | HG00558.hp2 HG00642.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.2175+87G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795443 | |||||||
chr16:795443 | G | GC | 21 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(18): Show |
22 | HG00741.hp2 HG01256.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.2175+94dupC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795443 | ||||||
chr16:795443 | G | T | 5 | a0011c0020t0001g0021 a0011c0031t0001g0034 a0023c0038t0001g0212 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175+87G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795443 | |||||||
chr16:795445 | C | CCCCCCCG others(81): Show |
3 | a0002c0002t0001g0201 a0002c0002t0001g0205 a0053c0076t0001g0214 |
3 | NA18989.hp1 NA18989.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2175+94_2175+95ins others(88): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCCGT others(80): Show |
5 | a0014c0029t0001g0184 a0014c0029t0001g0185 a0014c0029t0001g0186 others(2): Show |
5 | HG00423.hp1 HG01123.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2175+94_2175+95ins others(87): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCCGT others(80): Show |
19 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(16): Show |
65 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2175+94_2175+95ins others(87): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCTGT others(83): Show |
4 | a0008c0008t0001g0005 a0009c0011t0001g0016 a0009c0027t0001g0091 others(1): Show |
14 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.2175+93_2175+94ins others(90): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCTGT others(131): Show |
1 | a0009c0011t0001g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2175+93_2175+94ins others(138): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCTGT others(489): Show |
1 | a0046c0053t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2175+93_2175+94ins others(496): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCTGT others(132): Show |
3 | a0003c0070t0002g0048 a0007c0030t0002g0048 a0007c0030t0002g0190 |
3 | HG00639.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2175+93_2175+94ins others(139): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795445 | C | CCCCCTGT others(80): Show |
3 | a0037c0069t0001g0053 a0038c0068t0001g0053 a0041c0046t0001g0230 |
3 | HG02976.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2175+93_2175+94ins others(87): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795445 | ||||||
chr16:795449 | CCAAA | C | 27 | a0001c0034t0002g0046 a0002c0002t0001g0204 a0002c0039t0001g0051 others(24): Show |
36 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.2175+96_2175+99del others(4): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795449 | ||||||
chr16:795451 | A | C | 4 | a0003c0072t0001g0075 a0004c0021t0001g0027 a0004c0021t0001g0058 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2175+95A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795451 | |||||||
chr16:795452 | A | C | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+96A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795452 | |||||||
chr16:795453 | A | C | 66 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(63): Show |
134 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2175+97A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795453 | |||||||
chr16:795454 | C | A | 2 | a0004c0021t0001g0027 a0036c0044t0001g0057 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2175+98C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795454 | |||||||
chr16:795454 | C | T | 21 | a0001c0034t0002g0046 a0004c0005t0002g0012 a0004c0005t0002g0026 others(18): Show |
28 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2175+98C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795454 | |||||||
chr16:795455 | A | G | 32 | a0001c0034t0002g0046 a0002c0002t0001g0204 a0002c0039t0001g0051 others(29): Show |
42 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175+99A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795455 | |||||||
chr16:795456 | C | T | 30 | a0001c0034t0002g0046 a0002c0002t0001g0204 a0002c0039t0001g0051 others(27): Show |
39 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.2175+100C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795456 | |||||||
chr16:795457 | A | G | 33 | a0001c0034t0002g0046 a0002c0002t0001g0204 a0002c0039t0001g0051 others(30): Show |
43 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175+101A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795457 | |||||||
chr16:795463 | C | T | 5 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0004c0021t0001g0027 others(2): Show |
9 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+107C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795463 | |||||||
chr16:795470 | C | G | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+114C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795470 | |||||||
chr16:795477 | C | T | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+121C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795477 | |||||||
chr16:795477 | CG | C | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+123delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795477 | ||||||
chr16:795479 | G | T | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+123G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795479 | |||||||
chr16:795483 | C | T | 5 | a0011c0020t0001g0021 a0011c0031t0001g0034 a0023c0038t0001g0212 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175+127C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795483 | |||||||
chr16:795484 | G | A | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+128G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795484 | |||||||
chr16:795486 | GC | G | 11 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(8): Show |
16 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.2175+133delC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795486 | ||||||
chr16:795489 | C | CT | 26 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(23): Show |
43 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.2175+133_2175+134i others(3): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795489 | |||||||
chr16:795489 | C | G | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+133C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795489 | |||||||
chr16:795489 | CG | C | 24 | a0002c0002t0001g0001 a0002c0002t0001g0025 a0002c0002t0001g0201 others(21): Show |
67 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.2175+134delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795489 | |||||||
chr16:795490 | G | C | 13 | a0002c0002t0001g0018 a0002c0002t0001g0209 a0002c0002t0001g0215 others(10): Show |
18 | HG01109.hp1 HG01517.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.2175+134G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795490 | |||||||
chr16:795490 | G | GC | 16 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(13): Show |
17 | HG01433.hp1 HG01433.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.2175+141dupC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795490 | ||||||
chr16:795490 | G | T | 26 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(23): Show |
43 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.2175+134G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795490 | |||||||
chr16:795492 | C | CCCCCTGT others(37): Show |
6 | a0002c0002t0001g0204 a0002c0039t0001g0051 a0015c0025t0001g0045 others(3): Show |
8 | HG01109.hp2 HG01261.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175+140_2175+141i others(46): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795492 | ||||||
chr16:795492 | C | CCCCCTGT others(37): Show |
1 | a0011c0020t0001g0021 | 3 | HG01069.hp1 HG01071.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2175+140_2175+141i others(46): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795492 | ||||||
chr16:795492 | C | CCCCCTGT others(85): Show |
3 | a0011c0031t0001g0034 a0023c0038t0001g0233 a0042c0071t0001g0211 |
4 | HG02280.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+140_2175+141i others(94): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795492 | ||||||
chr16:795492 | C | CCCCCTGT others(133): Show |
1 | a0023c0038t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2175+140_2175+141i others(142): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795492 | ||||||
chr16:795492 | C | T | 26 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(23): Show |
43 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.2175+136C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795492 | |||||||
chr16:795494 | C | G | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2175+138C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795494 | |||||||
chr16:795497 | CAAACACA others(57): Show |
C | 2 | a0018c0019t0001g0093 a0018c0019t0001g0094 |
2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2175+142_2176-124d others(66): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795497 | |||||||
chr16:795498 | A | C | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2175+142A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795498 | |||||||
chr16:795499 | A | C | 12 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(9): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2175+143A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795499 | |||||||
chr16:795499 | A | G | 1 | a0018c0019t0001g0095 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2175+143A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795499 | |||||||
chr16:795500 | A | ACACACTG others(321): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0003c0003t0001g0065 |
4 | HG01256.hp1 NA18993.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-142_2176-141i others(330): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795500 | ||||||
chr16:795500 | A | ACACACTG others(322): Show |
1 | a0001c0001t0001g0200 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2176-142_2176-141i others(331): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795500 | ||||||
chr16:795500 | A | ACACACTG others(322): Show |
1 | a0001c0001t0001g0037 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2176-142_2176-141i others(331): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795500 | ||||||
chr16:795500 | A | C | 78 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(75): Show |
151 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2175+144A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795500 | |||||||
chr16:795501 | C | A | 7 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0077 others(4): Show |
11 | HG00642.hp1 HG02080.hp2 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.2175+145C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795501 | |||||||
chr16:795501 | C | T | 6 | a0019c0026t0001g0033 a0019c0026t0001g0089 a0020c0018t0001g0031 others(3): Show |
9 | HG01099.hp2 HG01243.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+145C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795501 | |||||||
chr16:795502 | A | AG | 5 | a0006c0006t0001g0030 a0006c0006t0001g0078 a0006c0051t0001g0081 others(2): Show |
6 | HG00558.hp2 HG02602.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175+146_2175+147i others(3): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795502 | |||||||
chr16:795502 | A | C | 1 | a0018c0019t0001g0095 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2175+146A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795502 | |||||||
chr16:795502 | A | G | 16 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0006c0006t0001g0015 others(13): Show |
24 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2175+146A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795502 | |||||||
chr16:795503 | C | T | 9 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0019c0026t0001g0033 others(6): Show |
13 | HG01099.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2175+147C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795503 | |||||||
chr16:795504 | A | G | 21 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0006c0006t0001g0015 others(18): Show |
30 | HG00558.hp2 HG00642.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.2175+148A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795504 | |||||||
chr16:795504 | ACTGCCCG others(56): Show |
A | 1 | a0018c0019t0001g0095 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2175+150_2176-117d others(65): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795504 | ||||||
chr16:795510 | C | T | 12 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(9): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2175+154C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795510 | |||||||
chr16:795517 | C | G | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+161C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795517 | |||||||
chr16:795524 | C | T | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-161C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795524 | |||||||
chr16:795524 | CG | C | 12 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(9): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2176-159delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795524 | ||||||
chr16:795526 | G | T | 12 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(9): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2176-159G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795526 | |||||||
chr16:795531 | G | A | 12 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(9): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2176-154G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795531 | |||||||
chr16:795532 | T | C | 1 | a0015c0025t0001g0168 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2176-153T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795532 | |||||||
chr16:795533 | GC | G | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-149delC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795533 | ||||||
chr16:795536 | C | CCCCCCCG others(29): Show |
1 | a0006c0006t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2176-149_2176-148i others(38): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795536 | |||||||
chr16:795536 | C | CCCCCCGT others(28): Show |
10 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(7): Show |
15 | HG00642.hp1 HG02080.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.2176-149_2176-148i others(37): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795536 | |||||||
chr16:795536 | C | CCCCTGTG others(29): Show |
2 | a0019c0026t0001g0033 a0019c0026t0001g0089 |
3 | HG02647.hp1 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2176-149_2176-148i others(38): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795536 | |||||||
chr16:795536 | C | CT | 67 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(64): Show |
137 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2176-149_2176-148i others(3): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795536 | |||||||
chr16:795536 | C | G | 2 | a0003c0017t0001g0009 a0003c0067t0001g0009 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-149C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795536 | |||||||
chr16:795536 | CG | C | 6 | a0002c0002t0001g0204 a0002c0039t0001g0051 a0015c0025t0001g0045 others(3): Show |
7 | HG01109.hp2 HG01496.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176-148delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795536 | |||||||
chr16:795537 | G | C | 10 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0003c0070t0002g0048 others(7): Show |
14 | HG00558.hp2 HG00639.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.2176-148G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795537 | |||||||
chr16:795537 | G | GC | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0023 others(16): Show |
19 | HG01433.hp2 HG01496.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.2176-141dupC | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795537 | ||||||
chr16:795537 | G | GCCCCCCT others(37): Show |
3 | a0037c0069t0001g0053 a0038c0068t0001g0053 a0041c0046t0001g0230 |
3 | HG02976.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2176-142_2176-141i others(46): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795537 | ||||||
chr16:795537 | G | T | 67 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(64): Show |
137 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2176-148G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795537 | |||||||
chr16:795539 | C | T | 67 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(64): Show |
137 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2176-146C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795539 | |||||||
chr16:795540 | C | T | 8 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0010c0010t0001g0035 others(5): Show |
10 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2176-145C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795540 | |||||||
chr16:795541 | C | G | 2 | a0003c0017t0001g0009 a0003c0067t0001g0009 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-144C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795541 | |||||||
chr16:795542 | C | G | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-143C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795542 | |||||||
chr16:795544 | CAAA | C | 12 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0006c0006t0001g0015 others(9): Show |
20 | HG00642.hp1 HG02080.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2176-140_2176-138d others(5): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795544 | |||||||
chr16:795544 | CAAACACA | C | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-140_2176-134d others(9): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795544 | |||||||
chr16:795547 | A | C | 82 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(79): Show |
156 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.2176-138A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795547 | |||||||
chr16:795548 | C | T | 1 | a0028c0045t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2176-137C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795548 | |||||||
chr16:795549 | A | G | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2176-136A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795549 | |||||||
chr16:795550 | C | T | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2176-135C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795550 | |||||||
chr16:795551 | A | C | 2 | a0003c0017t0001g0009 a0003c0067t0001g0009 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-134A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795551 | |||||||
chr16:795551 | A | G | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2176-134A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795551 | |||||||
chr16:795553 | T | C | 5 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0004c0021t0001g0027 others(2): Show |
9 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2176-132T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795553 | |||||||
chr16:795557 | CGTGTGGC others(2): Show |
C | 5 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0004c0021t0001g0027 others(2): Show |
9 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2176-127_2176-119d others(11): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795557 | |||||||
chr16:795562 | G | C | 2 | a0018c0019t0001g0093 a0018c0019t0001g0094 |
2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2176-123G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795562 | |||||||
chr16:795564 | C | G | 11 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(8): Show |
16 | HG00642.hp1 HG02080.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.2176-121C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795564 | |||||||
chr16:795565 | T | C | 2 | a0018c0019t0001g0093 a0018c0019t0001g0094 |
2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2176-120T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795565 | |||||||
chr16:795566 | G | C | 2 | a0018c0019t0001g0093 a0018c0019t0001g0094 |
2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2176-119G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795566 | |||||||
chr16:795568 | C | A | 5 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0018c0019t0001g0093 others(2): Show |
6 | HG01109.hp1 HG02083.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-117C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795568 | |||||||
chr16:795568 | C | T | 2 | a0003c0017t0001g0009 a0003c0067t0001g0009 |
5 | HG02451.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-117C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795568 | |||||||
chr16:795571 | C | T | 11 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(8): Show |
16 | HG00642.hp1 HG02080.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.2176-114C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795571 | |||||||
chr16:795571 | CG | C | 4 | a0001c0001t0001g0219 a0006c0051t0001g0081 a0019c0026t0001g0033 others(1): Show |
6 | HG00558.hp2 HG01261.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-112delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795571 | ||||||
chr16:795572 | G | C | 7 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0004c0021t0001g0027 others(4): Show |
11 | HG01109.hp1 HG02083.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.2176-113G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795572 | |||||||
chr16:795572 | G | T | 3 | a0018c0019t0001g0095 a0019c0026t0001g0089 a0020c0018t0001g0087 |
3 | HG02647.hp1 HG03041.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2176-113G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795572 | |||||||
chr16:795573 | G | C | 3 | a0018c0019t0001g0095 a0019c0026t0001g0089 a0020c0018t0001g0087 |
3 | HG02647.hp1 HG03041.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2176-112G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795573 | |||||||
chr16:795573 | G | T | 10 | a0003c0017t0001g0009 a0003c0067t0001g0009 a0004c0021t0001g0027 others(7): Show |
16 | HG00558.hp2 HG01109.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2176-112G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795573 | |||||||
chr16:795574 | C | CCCATGCC others(125): Show |
1 | a0019c0026t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2176-109_2176-108i others(134): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795574 | ||||||
chr16:795574 | C | CCCATGCC others(96): Show |
1 | a0020c0018t0001g0087 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2176-109_2176-108i others(105): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795574 | ||||||
chr16:795577 | C | T | 1 | a0018c0019t0001g0095 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2176-108C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795577 | |||||||
chr16:795577 | CG | C | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-107delG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795577 | |||||||
chr16:795578 | G | A | 3 | a0006c0051t0001g0081 a0019c0026t0001g0033 a0020c0018t0001g0031 |
5 | HG00558.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-107G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795578 | |||||||
chr16:795578 | G | C | 3 | a0018c0019t0001g0095 a0019c0026t0001g0089 a0020c0018t0001g0087 |
3 | HG02647.hp1 HG03041.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2176-107G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795578 | |||||||
chr16:795578 | G | T | 2 | a0018c0019t0001g0093 a0018c0019t0001g0094 |
2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2176-107G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795578 | |||||||
chr16:795579 | T | C | 3 | a0018c0019t0001g0093 a0018c0019t0001g0094 a0018c0019t0001g0095 |
3 | HG02083.hp2 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2176-106T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795579 | |||||||
chr16:795580 | G | C | 8 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0018c0019t0001g0093 others(5): Show |
9 | HG01109.hp1 HG02083.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.2176-105G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795580 | |||||||
chr16:795580 | G | GCCCCACA others(261): Show |
2 | a0007c0030t0002g0048 a0007c0030t0002g0190 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(270): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCACA others(262): Show |
1 | a0003c0070t0002g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(271): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(115): Show |
1 | a0009c0027t0001g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(124): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(118): Show |
1 | a0009c0027t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(127): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(109): Show |
2 | a0009c0011t0001g0016 a0009c0011t0001g0096 |
5 | HG02647.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-102_2176-101i others(118): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(110): Show |
1 | a0008c0008t0001g0005 | 8 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2176-102_2176-101i others(119): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(146): Show |
2 | a0011c0020t0001g0021 a0028c0045t0001g0086 |
4 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-102_2176-101i others(155): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(147): Show |
1 | a0011c0031t0001g0034 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(156): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(149): Show |
1 | a0023c0038t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(158): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(151): Show |
1 | a0042c0071t0001g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(160): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(152): Show |
1 | a0023c0038t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(161): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(117): Show |
3 | a0037c0069t0001g0053 a0038c0068t0001g0053 a0041c0046t0001g0230 |
3 | HG02976.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(126): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(112): Show |
1 | a0015c0025t0001g0168 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(121): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(190): Show |
1 | a0046c0053t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(199): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(129): Show |
1 | a0019c0026t0001g0033 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(138): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(96): Show |
1 | a0020c0018t0001g0031 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(105): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(98): Show |
1 | a0020c0018t0001g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(107): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCCCCC others(53): Show |
1 | a0006c0051t0001g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(62): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(256): Show |
1 | a0007c0012t0003g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(265): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(311): Show |
1 | a0004c0048t0002g0012 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(320): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(163): Show |
1 | a0009c0027t0001g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(172): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(456): Show |
1 | a0021c0036t0004g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(465): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(332): Show |
1 | a0021c0036t0004g0032 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(341): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(257): Show |
1 | a0007c0012t0003g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(266): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(453): Show |
1 | a0001c0034t0002g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(462): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(406): Show |
1 | a0004c0005t0002g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(415): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(408): Show |
2 | a0004c0005t0002g0026 a0004c0005t0002g0221 |
2 | HG03486.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(417): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(410): Show |
1 | a0004c0005t0002g0231 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(419): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(407): Show |
2 | a0004c0005t0002g0012 a0004c0005t0002g0222 |
2 | HG00738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(416): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(371): Show |
1 | a0007c0030t0002g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(380): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(408): Show |
1 | a0004c0005t0002g0224 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(417): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(455): Show |
1 | a0001c0034t0002g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(464): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(407): Show |
1 | a0004c0013t0002g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(416): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(408): Show |
3 | a0004c0005t0002g0012 a0004c0005t0002g0220 a0004c0005t0002g0223 |
3 | HG02258.hp1 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(417): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(409): Show |
1 | a0004c0005t0002g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(418): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(410): Show |
1 | a0004c0013t0002g0229 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(419): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(409): Show |
1 | a0004c0005t0002g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(418): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(410): Show |
2 | a0004c0005t0002g0228 a0004c0013t0002g0226 |
2 | HG03579.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(419): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(373): Show |
1 | a0040c0047t0002g0012 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(382): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(413): Show |
1 | a0004c0013t0002g0227 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(422): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(208): Show |
1 | a0033c0066t0001g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(217): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(257): Show |
1 | a0007c0012t0003g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(266): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(258): Show |
1 | a0007c0012t0003g0055 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(267): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(303): Show |
2 | a0003c0007t0001g0008 a0034c0043t0001g0008 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(312): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(304): Show |
2 | a0003c0007t0001g0008 a0003c0007t0001g0192 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2176-102_2176-101i others(313): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(307): Show |
1 | a0007c0012t0003g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(316): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(352): Show |
3 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 |
5 | HG00735.hp1 HG01106.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-102_2176-101i others(361): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(448): Show |
1 | a0024c0042t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(457): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(497): Show |
1 | a0024c0042t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(506): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(67): Show |
1 | a0015c0025t0001g0045 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2176-102_2176-101i others(76): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(65): Show |
5 | a0002c0002t0001g0204 a0002c0039t0001g0051 a0016c0023t0001g0169 others(2): Show |
6 | HG01109.hp2 HG02683.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-102_2176-101i others(74): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCCTTCT others(66): Show |
1 | a0015c0025t0001g0045 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2176-102_2176-101i others(75): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCGCCCC others(16): Show |
4 | a0002c0002t0001g0001 a0002c0002t0001g0216 a0002c0002t0001g0237 others(1): Show |
13 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.2176-103_2176-102i others(25): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCGCCCC others(17): Show |
16 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0201 others(13): Show |
47 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.2176-103_2176-102i others(26): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCGCCCC others(18): Show |
5 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0014c0029t0001g0186 others(2): Show |
6 | HG02071.hp1 HG02083.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-103_2176-102i others(27): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCCGCCCC others(19): Show |
2 | a0025c0041t0001g0188 a0025c0041t0007g0187 |
2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2176-103_2176-102i others(28): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCGGCCCC others(13): Show |
2 | a0006c0006t0001g0082 a0045c0049t0001g0084 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2176-104_2176-103i others(22): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCGGCCCC others(14): Show |
9 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(6): Show |
13 | HG00642.hp1 HG02080.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176-104_2176-103i others(23): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795580 | G | GCGGCCCC others(15): Show |
1 | a0006c0006t0001g0030 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2176-104_2176-103i others(24): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795580 | ||||||
chr16:795581 | C | CCGCCCCG others(15): Show |
2 | a0002c0002t0001g0025 a0002c0002t0001g0209 |
4 | HG01516.hp2 HG01517.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-103_2176-102i others(24): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795581 | ||||||
chr16:795584 | G | C | 105 | a0001c0034t0002g0046 a0002c0002t0001g0001 a0002c0002t0001g0018 others(102): Show |
189 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.2176-101G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795584 | |||||||
chr16:795584 | G | GCCCCCCC others(710): Show |
1 | a0003c0003t0001g0028 | 2 | NA18971.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2176-95_2176-94ins others(717): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCCCC others(711): Show |
3 | a0001c0001t0001g0036 a0003c0003t0001g0019 a0003c0003t0001g0076 |
6 | HG02027.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-95_2176-94ins others(718): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCCCC others(712): Show |
1 | a0003c0003t0001g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2176-95_2176-94ins others(719): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCCCC others(712): Show |
1 | a0003c0003t0001g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2176-95_2176-94ins others(719): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCCCC others(712): Show |
1 | a0003c0003t0001g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2176-95_2176-94ins others(719): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCCCC others(713): Show |
1 | a0003c0003t0001g0062 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2176-95_2176-94ins others(720): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCCCC others(717): Show |
1 | a0003c0003t0001g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2176-95_2176-94ins others(724): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795584 | G | GCCCCTCC others(7): Show |
1 | a0002c0079t0001g0208 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2176-97_2176-96ins others(14): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795584 | ||||||
chr16:795591 | T | C | 114 | a0001c0001t0001g0036 a0001c0034t0002g0046 a0002c0002t0001g0001 others(111): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.2176-94T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795591 | |||||||
chr16:795593 | T | C | 115 | a0001c0001t0001g0036 a0001c0034t0002g0046 a0002c0002t0001g0001 others(112): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.2176-92T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795593 | |||||||
chr16:795593 | T | TGCTGCCC others(616): Show |
1 | a0001c0001t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(623): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(288): Show |
1 | a0003c0003t0001g0065 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(295): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(289): Show |
1 | a0001c0001t0001g0037 | 2 | NA18967.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(296): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(288): Show |
1 | a0001c0001t0001g0038 | 2 | NA18993.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(295): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(293): Show |
1 | a0005c0004t0001g0163 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(300): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(568): Show |
2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(575): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
7 | a0005c0004t0001g0056 a0005c0004t0001g0112 a0005c0004t0001g0164 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
5 | a0005c0004t0001g0007 a0005c0004t0001g0107 a0012c0015t0001g0007 others(2): Show |
9 | HG00738.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0012c0015t0001g0114 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0005c0004t0001g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0043c0054t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0005c0004t0001g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0005c0004t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0005c0004t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0012c0015t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(669): Show |
1 | a0005c0004t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(676): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0052c0059t0001g0195 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(619): Show |
1 | a0001c0001t0001g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(626): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(618): Show |
1 | a0001c0001t0001g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(625): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(18): Show |
43 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(663): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0125 others(10): Show |
25 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(670): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0128 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
1 | a0001c0001t0001g0129 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(619): Show |
1 | a0003c0003t0001g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(626): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(663): Show |
1 | a0003c0003t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(670): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0174 |
5 | HG00642.hp2 HG02071.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0196 |
4 | NA18952.hp2 NA18971.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(663): Show |
1 | a0001c0001t0001g0011 | 5 | NA18954.hp2 NA18978.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(670): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0197 |
2 | NA18997.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0131 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
1 | a0003c0003t0001g0068 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0005c0004t0001g0132 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0003c0073t0001g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0133 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(617): Show |
1 | a0001c0001t0001g0134 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(624): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(616): Show |
1 | a0001c0001t0001g0040 | 2 | NA18942.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(623): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(853): Show |
1 | a0003c0003t0001g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(860): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(521): Show |
1 | a0003c0003t0001g0071 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(528): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
1 | a0001c0001t0001g0136 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(669): Show |
1 | a0005c0004t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(676): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(618): Show |
1 | a0049c0061t0001g0142 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(625): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(672): Show |
1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(679): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0001c0001t0001g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(433): Show |
1 | a0001c0001t0001g0145 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(440): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(708): Show |
1 | a0001c0001t0001g0106 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(715): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
1 | a0001c0001t0001g0218 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0146 others(5): Show |
24 | HG00099.hp2 HG00673.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(664): Show |
2 | a0001c0001t0001g0022 a0030c0074t0001g0173 |
4 | HG00733.hp1 HG01981.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(671): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0041 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(708): Show |
1 | a0001c0016t0001g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(715): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
2 | a0001c0001t0001g0042 a0003c0007t0001g0183 |
3 | HG01081.hp1 HG01993.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG00741.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(665): Show |
1 | a0001c0001t0001g0049 | 2 | NA18975.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
2 | a0001c0024t0001g0151 a0003c0003t0001g0072 |
2 | HG01433.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(617): Show |
1 | a0001c0001t0001g0180 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(624): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(619): Show |
1 | a0001c0001t0001g0110 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(626): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0022c0035t0001g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
2 | a0001c0001t0001g0166 a0003c0003t0001g0073 |
2 | HG00408.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0001c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0001c0001t0001g0155 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0001c0001t0001g0157 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0001c0001t0001g0158 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0001c0001t0001g0159 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(1058): Show |
1 | a0003c0003t0001g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(1065): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(667): Show |
1 | a0001c0001t0001g0199 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(674): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(668): Show |
1 | a0001c0001t0001g0219 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(675): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(616): Show |
1 | a0013c0014t0001g0043 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(623): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(615): Show |
1 | a0013c0014t0001g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(622): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(616): Show |
1 | a0013c0014t0001g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(623): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(569): Show |
1 | a0001c0016t0001g0044 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(576): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(570): Show |
1 | a0001c0016t0001g0160 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(577): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(289): Show |
1 | a0001c0001t0001g0200 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(296): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(663): Show |
1 | a0003c0072t0001g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(670): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795593 | T | TGCTGCCC others(666): Show |
1 | a0001c0001t0001g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(673): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795593 | ||||||
chr16:795603 | G | A | 20 | a0001c0034t0002g0046 a0003c0070t0002g0048 a0004c0005t0002g0012 others(17): Show |
25 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2176-82G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795603 | |||||||
chr16:795610 | C | CCCCCGGC others(289): Show |
2 | a0010c0010t0001g0035 a0010c0010t0001g0105 |
3 | NA18747.hp1 NA18946.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2176-73_2176-72ins others(296): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795610 | ||||||
chr16:795610 | C | CCCCCGGC others(288): Show |
1 | a0010c0010t0001g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(295): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795610 | ||||||
chr16:795610 | C | CCCCCGGC others(244): Show |
1 | a0010c0064t0001g0103 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(251): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795610 | ||||||
chr16:795610 | C | CCCCCGGC others(291): Show |
1 | a0010c0010t0001g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(298): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795610 | ||||||
chr16:795610 | C | CCCCCGGC others(665): Show |
1 | a0001c0009t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2176-73_2176-72ins others(672): Show |
CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 795610 | ||||||
chr16:795627 | A | G | 6 | a0008c0008t0001g0005 a0009c0011t0001g0016 a0009c0011t0001g0096 others(3): Show |
16 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.2176-58A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795627 | |||||||
chr16:795638 | G | A | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2176-47G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795638 | |||||||
chr16:795676 | C | G | 1 | a0004c0005t0002g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2176-9C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 16/21 | chr16 | 795676 | |||||||
chr16:795943 | C | G | 1 | a0001c0009t0001g0127 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.2326-4C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 17/21 | chr16 | 795943 | |||||||
chr16:796084 | C | T | 3 | a0014c0029t0001g0184 a0014c0029t0001g0185 a0014c0029t0001g0186 |
3 | HG00423.hp1 HG01123.hp2 HG02083.hp1 |
splice_region_variant&intron_variant | LOW | c.2456+7C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796084 | |||||||
chr16:796182 | G | A | 1 | a0004c0013t0002g0229 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2456+105G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796182 | |||||||
chr16:796194 | C | T | 1 | a0003c0007t0001g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2456+117C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796194 | |||||||
chr16:796217 | C | T | 3 | a0004c0021t0001g0027 a0004c0021t0001g0058 a0036c0044t0001g0057 |
4 | HG01109.hp1 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2456+140C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796217 | |||||||
chr16:796289 | G | A | 1 | a0001c0032t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2456+212G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796289 | |||||||
chr16:796337 | C | T | 8 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(5): Show |
12 | HG00735.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.2456+260C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796337 | |||||||
chr16:796364 | C | T | 2 | a0020c0018t0001g0031 a0020c0018t0001g0087 |
3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2456+287C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796364 | |||||||
chr16:796372 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2456+295G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796372 | |||||||
chr16:796372 | G | T | 1 | a0014c0029t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2456+295G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796372 | |||||||
chr16:796445 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0005g0124 |
2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2457-272C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796445 | |||||||
chr16:796478 | C | T | 6 | a0008c0008t0001g0005 a0009c0011t0001g0016 a0009c0011t0001g0096 others(3): Show |
16 | HG01934.hp1 HG01943.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.2457-239C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796478 | |||||||
chr16:796563 | G | A | 1 | a0009c0027t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2457-154G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796563 | |||||||
chr16:796580 | C | T | 1 | a0009c0027t0001g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2457-137C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796580 | |||||||
chr16:796631 | G | A | 38 | a0003c0003t0001g0006 a0003c0003t0001g0013 a0003c0003t0001g0014 others(35): Show |
55 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.2457-86G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796631 | |||||||
chr16:796652 | C | T | 33 | a0002c0002t0001g0001 a0002c0002t0001g0018 a0002c0002t0001g0025 others(30): Show |
80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2457-65C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796652 | |||||||
chr16:796711 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02074.hp2 | splice_region_variant&intron_variant | LOW | c.2457-6G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 18/21 | chr16 | 796711 | |||||||
chr16:796915 | A | G | 9 | a0004c0005t0002g0012 a0004c0005t0002g0026 a0004c0005t0002g0222 others(6): Show |
13 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2602-46A>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/21 | chr16 | 796915 | |||||||
chr16:796934 | A | C | 19 | a0001c0034t0002g0046 a0003c0070t0002g0048 a0004c0005t0002g0012 others(16): Show |
24 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2602-27A>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 19/21 | chr16 | 796934 | |||||||
chr16:797112 | G | T | 8 | a0003c0007t0001g0008 a0003c0007t0001g0047 a0003c0007t0001g0191 others(5): Show |
12 | HG00735.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.2733+20G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797112 | |||||||
chr16:797113 | G | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0049 others(8): Show |
18 | HG00438.hp2 HG02027.hp2 NA18952.hp2 others(15): Show |
intron_variant | MODIFIER | c.2733+21G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797113 | |||||||
chr16:797136 | T | C | 20 | a0001c0034t0002g0046 a0003c0070t0002g0048 a0004c0005t0002g0012 others(17): Show |
25 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2733+44T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797136 | |||||||
chr16:797165 | G | T | 1 | a0007c0012t0003g0232 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2733+73G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797165 | |||||||
chr16:797183 | T | TG | 2 | a0009c0011t0001g0016 a0009c0011t0001g0096 |
5 | HG02647.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2733+95dupG | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 797183 | ||||||
chr16:797207 | T | G | 46 | a0001c0034t0002g0046 a0003c0070t0002g0048 a0004c0005t0002g0012 others(43): Show |
61 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.2733+115T>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797207 | |||||||
chr16:797212 | G | A | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2733+120G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797212 | |||||||
chr16:797248 | C | T | 3 | a0007c0012t0003g0054 a0007c0012t0003g0055 a0007c0012t0003g0232 |
5 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2733+156C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797248 | |||||||
chr16:797262 | C | G | 1 | a0018c0019t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2733+170C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797262 | |||||||
chr16:797342 | G | T | 1 | a0002c0002t0001g0207 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2733+250G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797342 | |||||||
chr16:797388 | G | A | 20 | a0001c0034t0002g0046 a0003c0070t0002g0048 a0004c0005t0002g0012 others(17): Show |
25 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2733+296G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797388 | |||||||
chr16:797425 | C | T | 2 | a0024c0042t0001g0235 a0024c0042t0001g0236 |
2 | HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2734-269C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797425 | |||||||
chr16:797469 | C | T | 1 | a0009c0027t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2734-225C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797469 | |||||||
chr16:797477 | G | T | 14 | a0001c0001t0001g0218 a0006c0006t0001g0015 a0006c0006t0001g0020 others(11): Show |
19 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.2734-217G>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797477 | |||||||
chr16:797491 | G | A | 2 | a0020c0018t0001g0031 a0020c0018t0001g0087 |
3 | HG02717.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2734-203G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797491 | |||||||
chr16:797537 | G | C | 6 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0133 others(3): Show |
6 | HG02040.hp2 HG03834.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.2734-157G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797537 | |||||||
chr16:797591 | T | C | 19 | a0001c0001t0001g0218 a0006c0006t0001g0015 a0006c0006t0001g0020 others(16): Show |
27 | HG00558.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2734-103T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797591 | |||||||
chr16:797597 | T | C | 107 | a0001c0001t0001g0218 a0001c0034t0002g0046 a0002c0002t0001g0001 others(104): Show |
191 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.2734-97T>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797597 | |||||||
chr16:797605 | C | A | 13 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(10): Show |
18 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2734-89C>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797605 | |||||||
chr16:797621 | G | C | 3 | a0007c0012t0003g0054 a0007c0012t0003g0055 a0007c0012t0003g0232 |
5 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2734-73G>C | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797621 | |||||||
chr16:797667 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2734-27C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797667 | |||||||
chr16:797674 | C | T | 2 | a0005c0004t0001g0112 a0029c0055t0001g0113 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2734-20C>T | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 20/21 | chr16 | 797674 | |||||||
chr16:797791 | G | A | 12 | a0006c0006t0001g0015 a0006c0006t0001g0020 a0006c0006t0001g0030 others(9): Show |
17 | HG00558.hp2 HG00642.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2791+40G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 21/21 | chr16 | 797791 | |||||||
chr16:797824 | C | G | 1 | a0002c0075t0001g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2792-15C>G | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 21/21 | chr16 | 797824 | |||||||
chr16:797835 | G | A | 5 | a0011c0020t0001g0021 a0011c0031t0001g0034 a0023c0038t0001g0212 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2792-4G>A | CHTF18 | ENSG00000127586.17 | transcript | ENST00000262315.14 | protein_coding | 21/21 | chr16 | 797835 |