Item | Value |
---|---|
geneid | 10036 |
ensemblid | ENSG00000167670.16 |
hgncid | 1910 |
symbol | CHAF1A |
name | chromatin assembly factor 1 subunit A |
refseq_nuc | NM_005483.3 |
refseq_prot | NP_005474.2 |
ensembl_nuc | ENST00000301280.10 |
ensembl_prot | ENSP00000301280.4 |
mane_status | MANE Select |
chr | chr19 |
start | 4402640 |
end | 4443397 |
strand | + |
ver | v1.2 |
region | chr19:4402640-4443397 |
region5000 | chr19:4397640-4448397 |
regionname0 | CHAF1A_chr19_4402640_4443397 |
regionname5000 | CHAF1A_chr19_4397640_4448397 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 956 | 225 | 45 | 50 | 101 | 9 | 19 | 75 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0002 | 1/0 | 956 | 114 | 20 | 19 | 49 | 7 | 18 | 41 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0003 | 0/0 | 956 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0004 | 0/0 | 956 | 11 | 2 | 0 | 7 | 0 | 2 | 5 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0005 | 0/0 | 956 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0006 | 0/0 | 956 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0007 | 0/0 | 956 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0008 | 0/0 | 956 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0009 | 0/0 | 956 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0010 | 0/0 | 956 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0011 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0012 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0013 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0014 | 0/0 | 956 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0015 | 0/0 | 956 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(951): Show |
chr19 | 4397640 | 4448397 |
a0016 | 0/0 | 254 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | MLEEL others(249): Show |
chr19 | 4397640 | 4448397 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2868 | 171 | 36 | 23 | 95 | 4 | 12 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0001c0003 | 0/0 | 2868 | 46 | 5 | 27 | 2 | 5 | 7 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0001c0007 | 0/0 | 2868 | 4 | 4 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0001c0020 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0001c0021 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0001c0022 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0001c0026 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0002c0002 | 1/0 | 2868 | 110 | 17 | 18 | 49 | 7 | 18 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0002c0011 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0002c0012 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0002c0023 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0003c0004 | 0/0 | 2868 | 12 | 12 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0004c0005 | 0/0 | 2868 | 11 | 2 | 0 | 7 | 0 | 2 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0005c0006 | 0/0 | 2868 | 6 | 6 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0005c0018 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0006c0008 | 0/0 | 2868 | 3 | 0 | 0 | 0 | 0 | 3 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0007c0010 | 0/0 | 2868 | 2 | 1 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0008c0009 | 0/0 | 2868 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0009c0019 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0010c0015 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0011c0025 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0012c0014 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0013c0013 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0014c0016 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0015c0017 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2863): Show |
chr19 | 4397640 | 4448397 | ||
a0016c0024 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | ATGCT others(2883): Show |
chr19 | 4397640 | 4448397 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3366 | 158 | 33 | 22 | 86 | 4 | 12 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0001c0001t0003 | 0/0 | 3375 | 9 | 3 | 0 | 6 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0001t0004 | 0/0 | 3375 | 3 | 0 | 0 | 3 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0001t0010 | 0/0 | 3375 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0003t0003 | 0/0 | 3375 | 41 | 3 | 25 | 1 | 5 | 7 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0003t0005 | 0/0 | 3375 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0003t0007 | 0/0 | 3376 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3371): Show |
chr19 | 4397640 | 4448397 |
a0001c0003t0008 | 0/0 | 3375 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0003t0009 | 0/0 | 3375 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0001c0007t0001 | 0/0 | 3366 | 4 | 4 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0001c0020t0001 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0001c0021t0001 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0001c0022t0001 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0001c0026t0001 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0002c0002t0002 | 1/0 | 3366 | 109 | 17 | 17 | 49 | 7 | 18 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0002c0002t0011 | 0/0 | 3366 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0002c0011t0002 | 0/0 | 3366 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0002c0012t0002 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0002c0023t0002 | 0/0 | 3366 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0003c0004t0002 | 0/0 | 3366 | 12 | 12 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0004c0005t0002 | 0/0 | 3366 | 11 | 2 | 0 | 7 | 0 | 2 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0005c0006t0002 | 0/0 | 3366 | 6 | 6 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0005c0018t0002 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0006c0008t0003 | 0/0 | 3375 | 3 | 0 | 0 | 0 | 0 | 3 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0007c0010t0006 | 0/0 | 3366 | 2 | 1 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0008c0009t0001 | 0/0 | 3366 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0009c0019t0002 | 0/0 | 3366 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0010c0015t0003 | 0/0 | 3375 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3370): Show |
chr19 | 4397640 | 4448397 |
a0011c0025t0002 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0012c0014t0001 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0013c0013t0002 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0014c0016t0002 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0015c0017t0002 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3361): Show |
chr19 | 4397640 | 4448397 |
a0016c0024t0002 | 0/0 | 3386 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | CAAAT others(3381): Show |
chr19 | 4397640 | 4448397 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0001t0010g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0003t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0007t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0020t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0021t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0022t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0001c0026t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0002t0011g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0011t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0011t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0012t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0002c0023t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0003c0004t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0004c0005t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0006t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0006t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0006t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0006t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0006t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0006t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0005c0018t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0006c0008t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0006c0008t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0006c0008t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0007c0010t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0007c0010t0006g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0008c0009t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0008c0009t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0009c0019t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0010c0015t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0011c0025t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0012c0014t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0013c0013t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0014c0016t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0015c0017t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
a0016c0024t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00099 | hp2 | a0001 | c0003 | t0003 | g0277 | EUR | GBR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00280 | hp1 | a0001 | c0003 | t0003 | g0303 | EUR | FIN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0042 | EUR | FIN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0016 | EUR | FIN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0309 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00544 | hp2 | a0001 | c0022 | t0001 | g0135 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00639 | hp2 | a0001 | c0003 | t0003 | g0012 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00642 | hp1 | a0001 | c0003 | t0003 | g0011 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00733 | hp2 | a0001 | c0003 | t0003 | g0321 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00735 | hp1 | a0007 | c0010 | t0006 | g0368 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00738 | hp2 | a0008 | c0009 | t0001 | g0161 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01069 | hp2 | a0001 | c0003 | t0003 | g0013 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01070 | hp2 | a0001 | c0003 | t0003 | g0287 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01071 | hp2 | a0001 | c0003 | t0003 | g0013 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01099 | hp1 | a0001 | c0003 | t0003 | g0296 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01099 | hp2 | a0002 | c0002 | t0011 | g0077 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01109 | hp1 | a0001 | c0003 | t0003 | g0290 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01109 | hp2 | a0002 | c0023 | t0002 | g0366 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01167 | hp1 | a0001 | c0003 | t0003 | g0284 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01167 | hp2 | a0009 | c0019 | t0002 | g0362 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01169 | hp1 | a0001 | c0003 | t0003 | g0285 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0307 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01192 | hp2 | a0001 | c0003 | t0003 | g0322 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01243 | hp1 | a0008 | c0009 | t0001 | g0162 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01255 | hp1 | a0010 | c0015 | t0003 | g0291 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01256 | hp1 | a0001 | c0003 | t0005 | g0301 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0119 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01257 | hp2 | a0001 | c0003 | t0003 | g0305 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01258 | hp2 | a0001 | c0003 | t0005 | g0300 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01346 | hp2 | a0001 | c0003 | t0003 | g0304 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01361 | hp2 | a0001 | c0003 | t0003 | g0283 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01515 | hp1 | a0001 | c0003 | t0003 | g0317 | EUR | IBS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0095 | EUR | IBS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0076 | EUR | IBS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01517 | hp1 | a0001 | c0003 | t0003 | g0316 | EUR | IBS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0078 | EUR | IBS | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01891 | hp1 | a0007 | c0010 | t0006 | g0367 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01928 | hp1 | a0001 | c0003 | t0003 | g0310 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01928 | hp2 | a0001 | c0003 | t0003 | g0293 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01934 | hp1 | a0001 | c0003 | t0003 | g0011 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0318 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01952 | hp1 | a0001 | c0003 | t0003 | g0302 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01975 | hp2 | a0001 | c0003 | t0003 | g0289 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02055 | hp2 | a0002 | c0011 | t0002 | g0281 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02071 | hp2 | a0001 | c0020 | t0001 | g0136 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02080 | hp1 | a0004 | c0005 | t0002 | g0350 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02145 | hp2 | a0001 | c0003 | t0009 | g0286 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02148 | hp1 | a0001 | c0003 | t0003 | g0306 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | CDX | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | CDX | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02273 | hp2 | a0001 | c0003 | t0003 | g0292 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02300 | hp1 | a0001 | c0003 | t0003 | g0298 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02523 | hp2 | a0004 | c0005 | t0002 | g0354 | EAS | KHV | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02602 | hp1 | a0001 | c0003 | t0003 | g0278 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0067 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02630 | hp2 | a0003 | c0004 | t0002 | g0337 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0297 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02717 | hp1 | a0003 | c0004 | t0002 | g0334 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02818 | hp1 | a0005 | c0018 | t0002 | g0363 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02886 | hp1 | a0001 | c0003 | t0008 | g0312 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0094 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02895 | hp1 | a0003 | c0004 | t0002 | g0336 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02895 | hp2 | a0001 | c0007 | t0001 | g0190 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02896 | hp2 | a0005 | c0006 | t0002 | g0359 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02897 | hp1 | a0005 | c0006 | t0002 | g0358 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02897 | hp2 | a0003 | c0004 | t0002 | g0335 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02922 | hp1 | a0003 | c0004 | t0002 | g0338 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02970 | hp1 | a0002 | c0011 | t0002 | g0282 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02970 | hp2 | a0005 | c0006 | t0002 | g0357 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02976 | hp1 | a0011 | c0025 | t0002 | g0333 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02976 | hp2 | a0003 | c0004 | t0002 | g0332 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03017 | hp1 | a0001 | c0003 | t0003 | g0280 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03041 | hp1 | a0003 | c0004 | t0002 | g0342 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03041 | hp2 | a0001 | c0007 | t0001 | g0176 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03139 | hp2 | a0001 | c0003 | t0003 | g0319 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0355 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03195 | hp2 | a0002 | c0012 | t0002 | g0365 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03209 | hp2 | a0003 | c0004 | t0002 | g0341 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03225 | hp1 | a0005 | c0006 | t0002 | g0360 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03225 | hp2 | a0012 | c0014 | t0001 | g0229 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03239 | hp2 | a0001 | c0003 | t0003 | g0294 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03486 | hp1 | a0003 | c0004 | t0002 | g0344 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03490 | hp1 | a0001 | c0003 | t0003 | g0279 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0086 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0069 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0088 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0070 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03516 | hp1 | a0005 | c0006 | t0002 | g0356 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | ESN | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0068 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0021 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0089 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03710 | hp1 | a0004 | c0005 | t0002 | g0014 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | PJL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0080 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0043 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0295 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03942 | hp2 | a0006 | c0008 | t0003 | g0315 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04115 | hp1 | a0006 | c0008 | t0003 | g0299 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0104 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | BEB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04199 | hp2 | a0001 | c0003 | t0003 | g0308 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04228 | hp1 | a0004 | c0005 | t0002 | g0348 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG04228 | hp2 | a0006 | c0008 | t0003 | g0314 | SAS | STU | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | YRI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18522 | hp2 | a0013 | c0013 | t0002 | g0364 | AFR | YRI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | CHB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18906 | hp2 | a0005 | c0006 | t0002 | g0361 | AFR | YRI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18944 | hp2 | a0004 | c0005 | t0002 | g0346 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18945 | hp2 | a0004 | c0005 | t0002 | g0351 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18974 | hp1 | a0004 | c0005 | t0002 | g0345 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18979 | hp2 | a0001 | c0021 | t0001 | g0141 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18985 | hp1 | a0014 | c0016 | t0002 | g0075 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18989 | hp1 | a0004 | c0005 | t0002 | g0353 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19000 | hp2 | a0004 | c0005 | t0002 | g0347 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19006 | hp1 | a0001 | c0003 | t0007 | g0313 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19030 | hp1 | a0001 | c0007 | t0001 | g0124 | AFR | LWK | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | LWK | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19055 | hp1 | a0015 | c0017 | t0002 | g0090 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19070 | hp1 | a0001 | c0026 | t0001 | g0002 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19076 | hp2 | a0016 | c0024 | t0002 | g0102 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ASW | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20129 | hp2 | a0001 | c0003 | t0003 | g0320 | AFR | ASW | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0057 | EUR | TSI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0061 | EUR | TSI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20805 | hp2 | a0001 | c0003 | t0003 | g0012 | EUR | TSI | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | GIH | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG01123 | hp2 | a0001 | c0003 | t0003 | g0311 | AMR | CLM | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02109 | hp2 | a0003 | c0004 | t0002 | g0340 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02486 | hp1 | a0003 | c0004 | t0002 | g0343 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02559 | hp1 | a0001 | c0007 | t0001 | g0204 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03471 | hp1 | a0004 | c0005 | t0002 | g0349 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG03471 | hp2 | a0003 | c0004 | t0002 | g0339 | AFR | MSL | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | USA | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
HG06807 | hp2 | a0004 | c0005 | t0002 | g0352 | AFR | USA | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | USA | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA20300 | hp2 | a0001 | c0003 | t0003 | g0288 | AFR | USA | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0079 | AFR | LWK | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0156 | REF | REF | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0014 | REF | REF | CHAF1A_chr19_4397640_4448397 | CHAF1A | chr19 | 4397640 | 4448397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4409176 | A | G | 1 | a0011 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.377A>G | p.Gln126Arg | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 500/3366 | 377/2871 | 126/956 | chr19 | 4409176 | |||
chr19:4409286 | G | A | 1 | a0012 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.487G>A | p.Ala163Thr | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 610/3366 | 487/2871 | 163/956 | chr19 | 4409286 | |||
chr19:4409299 | A | T | 1 | a0013 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.500A>T | p.Asp167Val | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 623/3366 | 500/2871 | 167/956 | chr19 | 4409299 | |||
chr19:4409436 | G | GGCCCGAG others(13): Show |
1 | a0016 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.638_657dupGCCCGAGA others(12): Show |
p.Lys220fs | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 781/3366 | 658/2871 | 220/956 | INFO_REALIGN_3_PRIME | chr19 | 4409436 | ||
chr19:4409469 | A | G | 1 | a0007 | 2 | HG00735.hp1 HG01891.hp1 |
missense_variant | MODERATE | c.670A>G | p.Ser224Gly | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 793/3366 | 670/2871 | 224/956 | chr19 | 4409469 | |||
chr19:4409514 | A | G | 2 | a0003 a0011 |
13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
missense_variant | MODERATE | c.715A>G | p.Met239Val | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 838/3366 | 715/2871 | 239/956 | chr19 | 4409514 | |||
chr19:4409634 | G | C | 1 | a0010 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.835G>C | p.Asp279His | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 958/3366 | 835/2871 | 279/956 | chr19 | 4409634 | |||
chr19:4422707 | C | T | 1 | a0008 | 2 | HG00738.hp2 HG01243.hp1 |
missense_variant | MODERATE | c.1159C>T | p.Arg387Trp | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 5/15 | 1282/3366 | 1159/2871 | 387/956 | chr19 | 4422707 | |||
chr19:4428859 | G | A | 1 | a0014 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.1573G>A | p.Val525Ile | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 8/15 | 1696/3366 | 1573/2871 | 525/956 | chr19 | 4428859 | |||
chr19:4429533 | G | A | 1 | a0015 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.1700G>A | p.Arg567Gln | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 9/15 | 1823/3366 | 1700/2871 | 567/956 | chr19 | 4429533 | |||
chr19:4432076 | C | T | 1 | a0006 | 3 | HG03942.hp2 HG04115.hp1 HG04228.hp2 |
missense_variant | MODERATE | c.2072C>T | p.Ala691Val | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/15 | 2195/3366 | 2072/2871 | 691/956 | chr19 | 4432076 | |||
chr19:4433256 | G | A | 1 | a0009 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.2390G>A | p.Arg797Gln | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/15 | 2513/3366 | 2390/2871 | 797/956 | chr19 | 4433256 | |||
chr19:4433415 | A | G | 2 | a0005 a0009 |
8 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.2549A>G | p.Lys850Arg | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/15 | 2672/3366 | 2549/2871 | 850/956 | chr19 | 4433415 | |||
chr19:4442339 | C | T | 5 | a0001 a0006 a0008 others(2): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
missense_variant&splice_region_variant | MODERATE | c.2768C>T | p.Ala923Val | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/15 | 2891/3366 | 2768/2871 | 923/956 | chr19 | 4442339 | |||
chr19:4443002 | G | T | 1 | a0004 | 11 | HG02080.hp1 HG02523.hp2 HG03471.hp1 others(8): Show |
missense_variant | MODERATE | c.2848G>T | p.Ala950Ser | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 15/15 | 2971/3366 | 2848/2871 | 950/956 | chr19 | 4443002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4408940 | G | A | 2 | a0002c0012 a0013c0013 |
2 | HG03195.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.141G>A | p.Lys47Lys | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 264/3366 | 141/2871 | 47/956 | chr19 | 4408940 | |||
chr19:4409009 | C | G | 1 | a0002c0011 | 2 | HG02055.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.210C>G | p.Ala70Ala | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 333/3366 | 210/2871 | 70/956 | chr19 | 4409009 | |||
chr19:4409057 | C | T | 1 | a0001c0026 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.258C>T | p.Asp86Asp | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 381/3366 | 258/2871 | 86/956 | chr19 | 4409057 | |||
chr19:4409759 | A | G | 3 | a0001c0003 a0006c0008 a0010c0015 |
50 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(47): Show |
splice_region_variant&synonymous_variant | LOW | c.960A>G | p.Arg320Arg | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/15 | 1083/3366 | 960/2871 | 320/956 | chr19 | 4409759 | |||
chr19:4428852 | C | G | 1 | a0002c0023 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1566C>G | p.Pro522Pro | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 8/15 | 1689/3366 | 1566/2871 | 522/956 | chr19 | 4428852 | |||
chr19:4432098 | C | T | 1 | a0001c0022 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.2094C>T | p.Gly698Gly | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/15 | 2217/3366 | 2094/2871 | 698/956 | chr19 | 4432098 | |||
chr19:4432194 | G | A | 1 | a0005c0018 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2190G>A | p.Arg730Arg | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/15 | 2313/3366 | 2190/2871 | 730/956 | chr19 | 4432194 | |||
chr19:4432200 | C | T | 1 | a0001c0021 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.2196C>T | p.Asp732Asp | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/15 | 2319/3366 | 2196/2871 | 732/956 | chr19 | 4432200 | |||
chr19:4433470 | G | A | 1 | a0001c0020 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.2604G>A | p.Ser868Ser | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/15 | 2727/3366 | 2604/2871 | 868/956 | chr19 | 4433470 | |||
chr19:4442283 | G | A | 1 | a0001c0007 | 4 | HG02559.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.2712G>A | p.Thr904Thr | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/15 | 2835/3366 | 2712/2871 | 904/956 | chr19 | 4442283 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4402662 | G | GGCGGCAG others(2): Show |
9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(6): Show |
62 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-95_-87dupAGCAGCGG others(1): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/15 | 86 | INFO_REALIGN_3_PRIME | chr19 | 4402662 | |||||
chr19:4402663 | G | GCGGCAGC others(3): Show |
1 | a0001c0003t0007 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99_-90dupCGGCAGCA others(2): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/15 | 89 | INFO_REALIGN_3_PRIME | chr19 | 4402663 | |||||
chr19:4402684 | G | C | 1 | a0001c0003t0008 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79G>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/15 | 79 | chr19 | 4402684 | ||||||
chr19:4402694 | G | C | 1 | a0001c0003t0005 | 2 | HG01256.hp1 HG01258.hp2 |
5_prime_UTR_variant | MODIFIER | c.-69G>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/15 | 69 | chr19 | 4402694 | ||||||
chr19:4402723 | C | G | 1 | a0007c0010t0006 | 2 | HG00735.hp1 HG01891.hp1 |
5_prime_UTR_variant | MODIFIER | c.-40C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/15 | 40 | chr19 | 4402723 | ||||||
chr19:4443049 | T | C | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0007t0001 others(6): Show |
171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*24T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 15/15 | 24 | chr19 | 4443049 | ||||||
chr19:4443318 | C | T | 1 | a0001c0001t0010 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 15/15 | 293 | chr19 | 4443318 | ||||||
chr19:4443342 | G | A | 1 | a0001c0003t0009 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 15/15 | 317 | chr19 | 4443342 | ||||||
chr19:4443348 | G | A | 1 | a0002c0002t0011 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 15/15 | 323 | chr19 | 4443348 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4402843 | G | A | 106 | a0001c0001t0001g0026 a0002c0002t0002g0001 a0002c0002t0002g0003 others(103): Show |
112 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.52+29G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4402843 | |||||||
chr19:4402852 | G | GGC | 4 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG01256.hp2 HG02280.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+44_52+45dupCG | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 4402852 | ||||||
chr19:4402939 | C | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(158): Show |
166 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.52+125C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4402939 | |||||||
chr19:4402940 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.52+126C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4402940 | |||||||
chr19:4403010 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03834.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.52+196A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403010 | |||||||
chr19:4403020 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(166): Show |
174 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.52+206A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403020 | |||||||
chr19:4403172 | G | A | 1 | a0001c0003t0003g0277 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.52+358G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403172 | |||||||
chr19:4403231 | G | GT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.52+418dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 4403231 | ||||||
chr19:4403264 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.52+450G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403264 | |||||||
chr19:4403284 | G | A | 3 | a0001c0003t0003g0278 a0001c0003t0003g0279 a0001c0003t0003g0280 |
3 | HG02602.hp1 HG03017.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.52+470G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403284 | |||||||
chr19:4403509 | G | A | 1 | a0002c0002t0002g0015 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.52+695G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403509 | |||||||
chr19:4403571 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.52+757C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403571 | |||||||
chr19:4403801 | T | C | 97 | a0001c0001t0001g0026 a0002c0002t0002g0001 a0002c0002t0002g0003 others(94): Show |
103 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.52+987T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403801 | |||||||
chr19:4403803 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.52+989T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403803 | |||||||
chr19:4403878 | C | A | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.52+1064C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403878 | |||||||
chr19:4403912 | C | G | 1 | a0002c0002t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.52+1098C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403912 | |||||||
chr19:4403960 | C | G | 1 | a0001c0001t0001g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.52+1146C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403960 | |||||||
chr19:4403973 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.52+1159C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4403973 | |||||||
chr19:4404358 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.52+1544T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404358 | |||||||
chr19:4404538 | G | A | 6 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 others(3): Show |
6 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-1374G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404538 | |||||||
chr19:4404623 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.53-1289A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404623 | |||||||
chr19:4404685 | T | G | 4 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(1): Show |
4 | NA18941.hp1 NA19012.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-1227T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404685 | |||||||
chr19:4404771 | A | T | 2 | a0002c0012t0002g0365 a0013c0013t0002g0364 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.53-1141A>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404771 | |||||||
chr19:4404818 | CT | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.53-1093delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404818 | |||||||
chr19:4404820 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.53-1092G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404820 | |||||||
chr19:4404821 | C | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.53-1091C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404821 | |||||||
chr19:4404822 | T | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.53-1090T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4404822 | |||||||
chr19:4405086 | C | G | 11 | a0002c0002t0002g0355 a0002c0012t0002g0365 a0005c0006t0002g0356 others(8): Show |
11 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-826C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405086 | |||||||
chr19:4405109 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.53-803T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405109 | |||||||
chr19:4405112 | T | C | 1 | a0002c0002t0002g0027 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.53-800T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405112 | |||||||
chr19:4405265 | A | G | 2 | a0002c0002t0002g0103 a0016c0024t0002g0102 |
2 | NA19003.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.53-647A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405265 | |||||||
chr19:4405397 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.53-515C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405397 | |||||||
chr19:4405480 | C | T | 4 | a0002c0002t0002g0098 a0002c0002t0002g0099 a0002c0002t0002g0100 others(1): Show |
4 | NA18939.hp2 NA18965.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-432C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405480 | |||||||
chr19:4405586 | C | T | 1 | a0004c0005t0002g0354 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.53-326C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405586 | |||||||
chr19:4405608 | C | CA | 10 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(7): Show |
10 | HG00741.hp1 HG01243.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-288dupA | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 4405608 | ||||||
chr19:4405624 | A | AT | 6 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG02027.hp2 HG02738.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-276dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 4405624 | ||||||
chr19:4405624 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.53-288A>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405624 | |||||||
chr19:4405642 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.53-270A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405642 | |||||||
chr19:4405714 | C | G | 3 | a0004c0005t0002g0350 a0004c0005t0002g0351 a0004c0005t0002g0353 |
3 | HG02080.hp1 NA18945.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.53-198C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405714 | |||||||
chr19:4405795 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.53-117G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 1/14 | chr19 | 4405795 | |||||||
chr19:4405996 | G | A | 9 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
9 | HG00423.hp2 HG00544.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+34G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4405996 | |||||||
chr19:4406163 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(210): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.103+201G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406163 | |||||||
chr19:4406244 | G | A | 2 | a0001c0001t0001g0271 a0001c0020t0001g0136 |
2 | HG02071.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.103+282G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406244 | |||||||
chr19:4406343 | C | G | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.103+381C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406343 | |||||||
chr19:4406365 | C | T | 2 | a0001c0003t0003g0321 a0001c0003t0003g0322 |
2 | HG00733.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.103+403C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406365 | |||||||
chr19:4406420 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.103+458C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406420 | |||||||
chr19:4406422 | G | A | 1 | a0003c0004t0002g0332 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103+460G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406422 | |||||||
chr19:4406433 | A | AT | 142 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
146 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.103+490dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4406433 | ||||||
chr19:4406433 | A | ATT | 30 | a0001c0001t0001g0010 a0001c0001t0001g0237 a0001c0001t0001g0238 others(27): Show |
31 | HG01261.hp2 HG01891.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.103+489_103+490dup others(2): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4406433 | ||||||
chr19:4406457 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.103+495C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406457 | |||||||
chr19:4406463 | C | T | 4 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0088 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+501C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406463 | |||||||
chr19:4406679 | T | C | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103+717T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4406679 | |||||||
chr19:4407089 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0270 |
3 | HG00673.hp1 HG02056.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.103+1127G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407089 | |||||||
chr19:4407099 | G | A | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.103+1137G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407099 | |||||||
chr19:4407103 | C | T | 1 | a0001c0001t0010g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.103+1141C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407103 | |||||||
chr19:4407109 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
6 | HG00423.hp1 HG02040.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.103+1147C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407109 | |||||||
chr19:4407135 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.103+1173T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407135 | |||||||
chr19:4407141 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.103+1179C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407141 | |||||||
chr19:4407144 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.103+1182G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407144 | |||||||
chr19:4407240 | C | G | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.103+1278C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407240 | |||||||
chr19:4407246 | C | A | 117 | a0001c0001t0001g0026 a0001c0001t0003g0323 a0001c0001t0003g0324 others(114): Show |
123 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.103+1284C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407246 | |||||||
chr19:4407246 | C | CA | 5 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1284_103+1285i others(3): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407246 | |||||||
chr19:4407247 | C | A | 147 | a0001c0001t0001g0026 a0001c0001t0003g0116 a0001c0001t0003g0117 others(144): Show |
153 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.103+1285C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407247 | |||||||
chr19:4407247 | CA | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.103+1294delA | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4407247 | ||||||
chr19:4407248 | A | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0021t0001g0141 |
3 | NA18959.hp2 NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.103+1286A>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407248 | |||||||
chr19:4407385 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.103+1423C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407385 | |||||||
chr19:4407461 | A | AG | 155 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.104-1441dupG | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4407461 | ||||||
chr19:4407462 | G | GGA | 7 | a0001c0001t0001g0128 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1441_104-1440i others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407462 | |||||||
chr19:4407465 | A | G | 7 | a0003c0004t0002g0338 a0003c0004t0002g0339 a0003c0004t0002g0340 others(4): Show |
7 | HG02109.hp2 HG02486.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-1438A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407465 | |||||||
chr19:4407475 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.104-1428C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407475 | |||||||
chr19:4407488 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.104-1415T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407488 | |||||||
chr19:4407781 | C | G | 2 | a0001c0003t0003g0316 a0001c0003t0003g0317 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.104-1122C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407781 | |||||||
chr19:4407891 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.104-1012T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4407891 | |||||||
chr19:4408057 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.104-846A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408057 | |||||||
chr19:4408059 | A | G | 357 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(354): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.104-844A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408059 | |||||||
chr19:4408151 | T | C | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.104-752T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408151 | |||||||
chr19:4408186 | C | A | 13 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(10): Show |
13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.104-717C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408186 | |||||||
chr19:4408192 | C | CT | 13 | a0001c0001t0001g0126 a0001c0001t0001g0227 a0001c0001t0001g0228 others(10): Show |
13 | HG00735.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-695dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408192 | ||||||
chr19:4408192 | CT | C | 9 | a0001c0001t0001g0271 a0001c0001t0003g0116 a0001c0001t0003g0117 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-695delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408192 | ||||||
chr19:4408207 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.104-696T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408207 | |||||||
chr19:4408285 | C | T | 2 | a0002c0012t0002g0365 a0013c0013t0002g0364 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.104-618C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408285 | |||||||
chr19:4408294 | A | G | 119 | a0001c0001t0001g0026 a0001c0001t0003g0323 a0001c0001t0003g0324 others(116): Show |
125 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.104-609A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408294 | |||||||
chr19:4408393 | C | T | 1 | a0001c0022t0001g0135 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.104-510C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408393 | |||||||
chr19:4408457 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104-446C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408457 | |||||||
chr19:4408461 | C | CT | 14 | a0001c0001t0001g0160 a0001c0003t0003g0280 a0001c0003t0003g0283 others(11): Show |
14 | HG00544.hp1 HG00738.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-412dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTT | 6 | a0001c0001t0010g0119 a0001c0003t0003g0319 a0001c0003t0003g0320 others(3): Show |
6 | HG01243.hp1 HG01256.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-413_104-412dup others(2): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTT | 6 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0002c0002t0002g0109 others(3): Show |
6 | HG02280.hp1 HG03579.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-414_104-412dup others(3): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTT | 10 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0002c0002t0002g0054 others(7): Show |
10 | HG00642.hp2 HG01175.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-417_104-412dup others(6): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT | 13 | a0002c0002t0002g0028 a0002c0002t0002g0059 a0002c0002t0002g0060 others(10): Show |
13 | HG01346.hp1 HG01496.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-418_104-412dup others(7): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(1): Show |
20 | a0001c0001t0001g0129 a0001c0001t0001g0164 a0001c0001t0001g0165 others(17): Show |
20 | HG00438.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.104-419_104-412dup others(8): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(2): Show |
11 | a0001c0001t0001g0166 a0001c0001t0003g0324 a0001c0001t0004g0325 others(8): Show |
11 | HG01099.hp2 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-420_104-412dup others(9): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(3): Show |
34 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0142 others(31): Show |
35 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.104-421_104-412dup others(10): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(4): Show |
33 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0143 others(30): Show |
34 | HG00099.hp1 HG01069.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.104-422_104-412dup others(11): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(5): Show |
17 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0196 others(14): Show |
18 | HG00673.hp2 HG02027.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.104-423_104-412dup others(12): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(6): Show |
14 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(11): Show |
14 | HG00733.hp1 HG01074.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-424_104-412dup others(13): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0214 a0001c0001t0001g0266 |
3 | HG00438.hp2 HG02300.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.104-425_104-412dup others(14): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0145 others(2): Show |
5 | HG00741.hp1 HG01243.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-426_104-412dup others(15): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0234 others(4): Show |
7 | HG02145.hp1 HG02165.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-427_104-412dup others(16): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0126 a0001c0001t0001g0217 a0001c0001t0001g0233 others(3): Show |
6 | HG00423.hp1 HG02523.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-428_104-412dup others(17): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG02040.hp2 NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.104-429_104-412dup others(18): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0003c0004t0002g0340 |
3 | HG02109.hp2 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.104-430_104-412dup others(19): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0236 a0001c0001t0001g0264 |
2 | HG01261.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.104-431_104-412dup others(20): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(14): Show |
3 | a0001c0001t0001g0223 a0003c0004t0002g0334 a0005c0006t0002g0360 |
3 | HG02717.hp1 HG03225.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.104-432_104-412dup others(21): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0130 |
2 | HG02132.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.104-433_104-412dup others(22): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0131 a0003c0004t0002g0335 a0003c0004t0002g0336 |
3 | HG00423.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.104-435_104-412dup others(24): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(18): Show |
1 | a0003c0004t0002g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.104-436_104-412dup others(25): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0132 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.104-437_104-412dup others(26): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0133 a0003c0004t0002g0337 |
2 | HG02630.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.104-438_104-412dup others(27): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.104-440_104-412dup others(29): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0265 |
2 | NA18952.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.104-441_104-412dup others(30): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(24): Show |
1 | a0001c0022t0001g0135 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.104-412_104-411ins others(31): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(26): Show |
1 | a0003c0004t0002g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.104-412_104-411ins others(33): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.104-412_104-411ins others(35): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(29): Show |
1 | a0003c0004t0002g0343 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.104-412_104-411ins others(36): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | C | CTTTTTTT others(47): Show |
1 | a0003c0004t0002g0344 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.104-412_104-411ins others(54): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | CTTTTTT | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0227 a0001c0001t0001g0239 others(18): Show |
22 | HG00621.hp1 HG00735.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.104-417_104-412del others(6): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | CTTTTTTT | C | 40 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(37): Show |
45 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.104-418_104-412del others(7): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.104-421_104-412del others(10): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
13 | HG00597.hp2 HG01109.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-422_104-412del others(11): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408461 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0271 a0007c0010t0006g0367 a0007c0010t0006g0368 |
3 | HG00735.hp1 HG01891.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.104-424_104-412del others(13): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 4408461 | ||||||
chr19:4408502 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.104-401C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408502 | |||||||
chr19:4408629 | A | G | 117 | a0001c0001t0001g0026 a0001c0001t0003g0323 a0001c0001t0003g0324 others(114): Show |
123 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.104-274A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408629 | |||||||
chr19:4408632 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.104-271G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408632 | |||||||
chr19:4408754 | A | G | 356 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(353): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.104-149A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 2/14 | chr19 | 4408754 | |||||||
chr19:4410006 | G | T | 2 | a0002c0002t0002g0005 a0002c0002t0002g0048 |
3 | HG01168.hp1 HG01169.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.960+247G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410006 | |||||||
chr19:4410090 | A | G | 1 | a0001c0001t0010g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.960+331A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410090 | |||||||
chr19:4410341 | A | G | 2 | a0003c0004t0002g0332 a0003c0004t0002g0337 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.960+582A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410341 | |||||||
chr19:4410348 | C | T | 1 | a0004c0005t0002g0348 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.960+589C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410348 | |||||||
chr19:4410386 | C | CT | 16 | a0001c0001t0001g0167 a0002c0002t0002g0082 a0002c0002t0002g0110 others(13): Show |
16 | HG00639.hp1 HG02109.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+643dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4410386 | ||||||
chr19:4410386 | C | CTT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.960+642_960+643dup others(2): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4410386 | ||||||
chr19:4410386 | C | CTTT | 6 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0263 others(3): Show |
6 | HG02155.hp2 HG02257.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+641_960+643dup others(3): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4410386 | ||||||
chr19:4410497 | C | T | 1 | a0002c0002t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.960+738C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410497 | |||||||
chr19:4410628 | G | A | 2 | a0002c0002t0002g0030 a0002c0002t0002g0031 |
2 | NA18950.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.960+869G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410628 | |||||||
chr19:4410649 | G | A | 43 | a0001c0003t0003g0011 a0001c0003t0003g0012 a0001c0003t0003g0013 others(40): Show |
46 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.960+890G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410649 | |||||||
chr19:4410792 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.960+1033A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410792 | |||||||
chr19:4410928 | T | C | 8 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(5): Show |
8 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+1169T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410928 | |||||||
chr19:4410974 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.960+1215C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4410974 | |||||||
chr19:4411315 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.960+1556C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411315 | |||||||
chr19:4411321 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(354): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.960+1562T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411321 | |||||||
chr19:4411378 | C | T | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.960+1619C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411378 | |||||||
chr19:4411408 | T | G | 1 | a0001c0001t0003g0326 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.960+1649T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411408 | |||||||
chr19:4411419 | G | A | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.960+1660G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411419 | |||||||
chr19:4411445 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(161): Show |
169 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.960+1686A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411445 | |||||||
chr19:4411591 | G | GA | 103 | a0001c0001t0001g0026 a0001c0001t0003g0323 a0001c0001t0003g0324 others(100): Show |
109 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.960+1838dupA | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411591 | ||||||
chr19:4411644 | C | CTTTTTTT others(3): Show |
3 | a0002c0002t0002g0065 a0002c0023t0002g0366 a0007c0010t0006g0368 |
3 | HG00438.hp1 HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.960+1897_960+1906d others(12): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(4): Show |
1 | a0002c0002t0002g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.960+1896_960+1906d others(13): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(5): Show |
4 | a0002c0002t0002g0003 a0002c0002t0002g0033 a0002c0002t0002g0067 others(1): Show |
5 | HG02602.hp2 HG03831.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1895_960+1906d others(14): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(6): Show |
4 | a0005c0006t0002g0358 a0005c0006t0002g0359 a0005c0006t0002g0360 others(1): Show |
4 | HG01167.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+1894_960+1906d others(15): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(7): Show |
1 | a0005c0006t0002g0356 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.960+1893_960+1906d others(16): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(8): Show |
7 | a0001c0003t0003g0287 a0002c0002t0002g0106 a0002c0002t0002g0112 others(4): Show |
7 | HG01070.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+1892_960+1906d others(17): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(9): Show |
23 | a0001c0003t0003g0283 a0001c0003t0003g0288 a0001c0003t0003g0289 others(20): Show |
23 | HG00544.hp1 HG01109.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.960+1891_960+1906d others(18): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(10): Show |
26 | a0001c0003t0003g0011 a0001c0003t0003g0012 a0001c0003t0003g0277 others(23): Show |
28 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.960+1890_960+1906d others(19): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(11): Show |
27 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(24): Show |
27 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.960+1889_960+1906d others(20): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(12): Show |
33 | a0001c0001t0003g0116 a0001c0001t0003g0118 a0001c0001t0004g0327 others(30): Show |
36 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.960+1888_960+1906d others(21): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(13): Show |
25 | a0001c0001t0003g0117 a0001c0001t0003g0328 a0001c0001t0003g0330 others(22): Show |
25 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.960+1887_960+1906d others(22): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(14): Show |
15 | a0001c0001t0001g0026 a0001c0003t0003g0279 a0002c0002t0002g0018 others(12): Show |
15 | HG00738.hp1 HG01071.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.960+1886_960+1906d others(23): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(15): Show |
9 | a0002c0002t0002g0021 a0002c0002t0002g0023 a0002c0002t0002g0024 others(6): Show |
9 | HG01515.hp2 HG01517.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+1906_960+1907i others(24): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0003g0331 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.960+1906_960+1907i others(26): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(18): Show |
1 | a0002c0002t0002g0022 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.960+1906_960+1907i others(27): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(19): Show |
2 | a0002c0002t0002g0005 a0002c0002t0002g0355 |
3 | HG01168.hp1 HG03195.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.960+1906_960+1907i others(28): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(20): Show |
1 | a0002c0002t0002g0048 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.960+1906_960+1907i others(29): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(23): Show |
1 | a0001c0003t0003g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.960+1906_960+1907i others(32): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | C | CTTTTTTT others(25): Show |
1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.960+1906_960+1907i others(34): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | CT | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0179 others(6): Show |
9 | HG00741.hp1 NA18946.hp1 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+1906delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411644 | CTT | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
155 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.960+1905_960+1906d others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4411644 | ||||||
chr19:4411687 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0239 a0001c0001t0001g0242 others(13): Show |
17 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+1928G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411687 | |||||||
chr19:4411704 | A | G | 357 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(354): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.960+1945A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411704 | |||||||
chr19:4411763 | T | C | 1 | a0001c0020t0001g0136 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.960+2004T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411763 | |||||||
chr19:4411805 | G | A | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.960+2046G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411805 | |||||||
chr19:4411809 | G | A | 1 | a0001c0007t0001g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.960+2050G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411809 | |||||||
chr19:4411839 | G | A | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.960+2080G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411839 | |||||||
chr19:4411860 | G | A | 1 | a0001c0003t0008g0312 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.960+2101G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411860 | |||||||
chr19:4411998 | G | A | 4 | a0001c0001t0001g0160 a0008c0009t0001g0161 a0008c0009t0001g0162 others(1): Show |
4 | HG00738.hp2 HG01243.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+2239G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4411998 | |||||||
chr19:4412051 | C | A | 1 | a0001c0003t0003g0293 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.960+2292C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412051 | |||||||
chr19:4412109 | T | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.960+2350T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412109 | |||||||
chr19:4412277 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.960+2518T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412277 | |||||||
chr19:4412437 | C | T | 1 | a0002c0002t0002g0046 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.960+2678C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412437 | |||||||
chr19:4412438 | G | A | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.960+2679G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412438 | |||||||
chr19:4412485 | G | A | 1 | a0002c0002t0002g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.960+2726G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412485 | |||||||
chr19:4412499 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.960+2740G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412499 | |||||||
chr19:4412662 | T | C | 5 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+2903T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412662 | |||||||
chr19:4412716 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.960+2957A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412716 | |||||||
chr19:4412754 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.960+2995G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412754 | |||||||
chr19:4412796 | A | G | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.960+3037A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412796 | |||||||
chr19:4412872 | C | T | 1 | a0001c0003t0003g0305 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.960+3113C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4412872 | |||||||
chr19:4413042 | G | C | 1 | a0002c0002t0002g0115 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.960+3283G>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413042 | |||||||
chr19:4413068 | CTTT | C | 18 | a0002c0002t0002g0003 a0002c0002t0002g0015 a0002c0002t0002g0033 others(15): Show |
19 | HG00621.hp1 HG02080.hp2 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.960+3313_960+3315d others(5): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4413068 | ||||||
chr19:4413076 | T | A | 1 | a0002c0002t0002g0034 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.960+3317T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413076 | |||||||
chr19:4413126 | G | A | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.960+3367G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413126 | |||||||
chr19:4413306 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.960+3547G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413306 | |||||||
chr19:4413316 | C | T | 1 | a0001c0003t0003g0292 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.960+3557C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413316 | |||||||
chr19:4413360 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.960+3601G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413360 | |||||||
chr19:4413421 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.960+3662C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413421 | |||||||
chr19:4413539 | A | G | 1 | a0002c0002t0002g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.960+3780A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413539 | |||||||
chr19:4413593 | A | G | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.960+3834A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413593 | |||||||
chr19:4413652 | G | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03834.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.960+3893G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413652 | |||||||
chr19:4413738 | C | T | 116 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(113): Show |
122 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.960+3979C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4413738 | |||||||
chr19:4414039 | G | A | 2 | a0001c0001t0001g0271 a0001c0020t0001g0136 |
2 | HG02071.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.961-3981G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414039 | |||||||
chr19:4414097 | T | C | 1 | a0002c0002t0002g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.961-3923T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414097 | |||||||
chr19:4414343 | G | C | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.961-3677G>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414343 | |||||||
chr19:4414396 | C | CA | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.961-3609dupA | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4414396 | ||||||
chr19:4414396 | C | CAA | 11 | a0001c0001t0001g0137 a0001c0001t0001g0163 a0001c0001t0001g0166 others(8): Show |
11 | HG00438.hp2 HG02523.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-3610_961-3609d others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4414396 | ||||||
chr19:4414412 | C | A | 2 | a0001c0001t0001g0026 a0002c0023t0002g0366 |
2 | HG01109.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.961-3608C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414412 | |||||||
chr19:4414556 | T | C | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.961-3464T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414556 | |||||||
chr19:4414597 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.961-3423A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414597 | |||||||
chr19:4414620 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.961-3400A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414620 | |||||||
chr19:4414686 | G | A | 1 | a0001c0001t0003g0328 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.961-3334G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414686 | |||||||
chr19:4414691 | C | T | 3 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0045 |
3 | HG00280.hp2 HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.961-3329C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414691 | |||||||
chr19:4414713 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.961-3307C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414713 | |||||||
chr19:4414824 | G | A | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.961-3196G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4414824 | |||||||
chr19:4415005 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.961-3015G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415005 | |||||||
chr19:4415008 | T | G | 94 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(91): Show |
100 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.961-3012T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415008 | |||||||
chr19:4415045 | C | G | 2 | a0002c0012t0002g0365 a0013c0013t0002g0364 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.961-2975C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415045 | |||||||
chr19:4415134 | C | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0221 |
2 | NA19054.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.961-2886C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415134 | |||||||
chr19:4415192 | T | C | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.961-2828T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415192 | |||||||
chr19:4415234 | ACTTCAAG others(3): Show |
A | 1 | a0015c0017t0002g0090 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.961-2784_961-2775d others(12): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4415234 | ||||||
chr19:4415304 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.961-2716T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415304 | |||||||
chr19:4415455 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.961-2565C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415455 | |||||||
chr19:4415470 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.961-2550A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415470 | |||||||
chr19:4415509 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.961-2511C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415509 | |||||||
chr19:4415510 | G | A | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.961-2510G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415510 | |||||||
chr19:4415524 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.961-2496C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415524 | |||||||
chr19:4415605 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.961-2415T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415605 | |||||||
chr19:4415792 | C | T | 10 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0266 others(7): Show |
10 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-2228C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415792 | |||||||
chr19:4415901 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.961-2119C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415901 | |||||||
chr19:4415932 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.961-2088G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4415932 | |||||||
chr19:4416167 | C | A | 1 | a0002c0002t0002g0059 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.961-1853C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416167 | |||||||
chr19:4416318 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0021t0001g0141 |
3 | NA18959.hp2 NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.961-1702C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416318 | |||||||
chr19:4416340 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.961-1680C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416340 | |||||||
chr19:4416399 | T | C | 1 | a0002c0012t0002g0365 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.961-1621T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416399 | |||||||
chr19:4416414 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.961-1606C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416414 | |||||||
chr19:4416461 | G | T | 1 | a0002c0002t0002g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-1559G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416461 | |||||||
chr19:4416646 | T | C | 1 | a0015c0017t0002g0090 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.961-1374T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416646 | |||||||
chr19:4416649 | G | T | 1 | a0015c0017t0002g0090 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.961-1371G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416649 | |||||||
chr19:4416654 | G | GC | 216 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(213): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.961-1365dupC | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4416654 | ||||||
chr19:4416655 | C | T | 1 | a0002c0002t0002g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.961-1365C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416655 | |||||||
chr19:4416660 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.961-1360C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416660 | |||||||
chr19:4416720 | A | G | 1 | a0002c0002t0002g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.961-1300A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416720 | |||||||
chr19:4416725 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.961-1295C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416725 | |||||||
chr19:4416768 | A | G | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.961-1252A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4416768 | |||||||
chr19:4417072 | C | T | 1 | a0002c0002t0002g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.961-948C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417072 | |||||||
chr19:4417246 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0026 others(28): Show |
33 | HG00423.hp1 HG01168.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.961-774C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417246 | |||||||
chr19:4417457 | C | CT | 127 | a0001c0001t0001g0226 a0001c0001t0003g0323 a0001c0001t0003g0324 others(124): Show |
136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.961-542dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4417457 | ||||||
chr19:4417457 | C | CTT | 18 | a0001c0001t0003g0331 a0001c0001t0004g0327 a0001c0003t0003g0277 others(15): Show |
18 | HG00099.hp2 HG00621.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.961-543_961-542dup others(2): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4417457 | ||||||
chr19:4417457 | CT | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.961-542delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 4417457 | ||||||
chr19:4417490 | T | C | 1 | a0002c0002t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.961-530T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417490 | |||||||
chr19:4417543 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.961-477C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417543 | |||||||
chr19:4417617 | C | T | 2 | a0001c0003t0005g0300 a0001c0003t0005g0301 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.961-403C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417617 | |||||||
chr19:4417641 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.961-379A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417641 | |||||||
chr19:4417647 | G | A | 2 | a0005c0018t0002g0363 a0009c0019t0002g0362 |
2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.961-373G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417647 | |||||||
chr19:4417672 | G | A | 1 | a0001c0007t0001g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.961-348G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417672 | |||||||
chr19:4417740 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.961-280C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417740 | |||||||
chr19:4417848 | T | C | 56 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(53): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.961-172T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417848 | |||||||
chr19:4417945 | A | G | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.961-75A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 3/14 | chr19 | 4417945 | |||||||
chr19:4418371 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1017+295C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4418371 | |||||||
chr19:4418409 | CT | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1017+357delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4418409 | ||||||
chr19:4418409 | CTT | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0173 a0001c0001t0001g0207 others(5): Show |
8 | HG01943.hp2 HG02027.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+356_1017+357d others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4418409 | ||||||
chr19:4418409 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0002g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1017+348_1017+357d others(12): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4418409 | ||||||
chr19:4418409 | CTTTTTTT others(4): Show |
C | 126 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(123): Show |
132 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1017+347_1017+357d others(13): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4418409 | ||||||
chr19:4418459 | A | G | 1 | a0002c0002t0002g0019 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1017+383A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4418459 | |||||||
chr19:4418518 | C | A | 43 | a0001c0003t0003g0011 a0001c0003t0003g0012 a0001c0003t0003g0013 others(40): Show |
46 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1017+442C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4418518 | |||||||
chr19:4418780 | G | A | 1 | a0001c0003t0003g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1017+704G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4418780 | |||||||
chr19:4418966 | G | A | 1 | a0002c0002t0002g0050 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1017+890G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4418966 | |||||||
chr19:4419029 | A | AT | 241 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
252 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1017+977dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4419029 | ||||||
chr19:4419029 | A | ATT | 32 | a0001c0001t0001g0122 a0001c0001t0001g0128 a0001c0001t0001g0129 others(29): Show |
32 | HG00621.hp1 HG00741.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1017+976_1017+977d others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4419029 | ||||||
chr19:4419029 | AT | A | 14 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0266 others(11): Show |
14 | HG00733.hp1 HG00738.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1017+977delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4419029 | ||||||
chr19:4419029 | ATTTTT | A | 11 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(8): Show |
11 | HG00621.hp2 HG00735.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1017+973_1017+977d others(7): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4419029 | ||||||
chr19:4419180 | G | A | 1 | a0002c0002t0002g0060 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1017+1104G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419180 | |||||||
chr19:4419340 | T | G | 2 | a0002c0002t0002g0092 a0002c0002t0002g0094 |
2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1017+1264T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419340 | |||||||
chr19:4419348 | T | C | 1 | a0002c0002t0002g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1017+1272T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419348 | |||||||
chr19:4419499 | G | A | 1 | a0005c0006t0002g0360 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1017+1423G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419499 | |||||||
chr19:4419586 | C | T | 1 | a0002c0012t0002g0365 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1017+1510C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419586 | |||||||
chr19:4419781 | A | T | 367 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(364): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1017+1705A>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419781 | |||||||
chr19:4419799 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1017+1723C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419799 | |||||||
chr19:4419825 | C | T | 1 | a0002c0002t0002g0027 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1017+1749C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419825 | |||||||
chr19:4419842 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1017+1766G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419842 | |||||||
chr19:4419996 | G | A | 2 | a0002c0002t0002g0082 a0002c0002t0002g0085 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1017+1920G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4419996 | |||||||
chr19:4420045 | T | C | 44 | a0001c0003t0003g0011 a0001c0003t0003g0012 a0001c0003t0003g0013 others(41): Show |
47 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1017+1969T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420045 | |||||||
chr19:4420159 | C | T | 14 | a0001c0003t0003g0012 a0001c0003t0003g0278 a0001c0003t0003g0279 others(11): Show |
15 | HG00280.hp1 HG00639.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1017+2083C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420159 | |||||||
chr19:4420164 | C | T | 2 | a0001c0003t0003g0316 a0001c0003t0003g0317 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1017+2088C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420164 | |||||||
chr19:4420245 | G | GT | 12 | a0001c0001t0004g0327 a0002c0002t0002g0015 a0002c0002t0002g0024 others(9): Show |
12 | HG00597.hp1 HG01934.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+2181dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4420245 | ||||||
chr19:4420245 | GT | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
157 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1017+2181delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4420245 | ||||||
chr19:4420246 | T | A | 1 | a0002c0002t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1017+2170T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420246 | |||||||
chr19:4420274 | G | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1017+2198G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420274 | |||||||
chr19:4420360 | G | A | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1018-2206G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420360 | |||||||
chr19:4420396 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(354): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1018-2170T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420396 | |||||||
chr19:4420418 | T | G | 1 | a0007c0010t0006g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1018-2148T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420418 | |||||||
chr19:4420667 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1018-1899C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420667 | |||||||
chr19:4420893 | T | C | 4 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG01256.hp2 HG02280.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-1673T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420893 | |||||||
chr19:4420933 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1018-1633A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4420933 | |||||||
chr19:4421216 | T | C | 1 | a0001c0007t0001g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1018-1350T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421216 | |||||||
chr19:4421221 | G | A | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1018-1345G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421221 | |||||||
chr19:4421278 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1018-1288T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421278 | |||||||
chr19:4421424 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1018-1142A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421424 | |||||||
chr19:4421514 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(354): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1018-1052T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421514 | |||||||
chr19:4421578 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1018-988A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421578 | |||||||
chr19:4421722 | G | A | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1018-844G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421722 | |||||||
chr19:4421800 | A | G | 13 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(10): Show |
13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-766A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421800 | |||||||
chr19:4421848 | T | C | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1018-718T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4421848 | |||||||
chr19:4421877 | C | CACTT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1018-688_1018-687i others(6): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 4421877 | ||||||
chr19:4422002 | T | C | 2 | a0001c0003t0003g0319 a0001c0003t0003g0320 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1018-564T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4422002 | |||||||
chr19:4422181 | T | A | 72 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0215 others(69): Show |
75 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-385T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4422181 | |||||||
chr19:4422182 | A | T | 1 | a0002c0012t0002g0365 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-384A>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4422182 | |||||||
chr19:4422238 | T | G | 2 | a0005c0006t0002g0358 a0005c0006t0002g0359 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1018-328T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4422238 | |||||||
chr19:4422245 | C | T | 8 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(5): Show |
8 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1018-321C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4422245 | |||||||
chr19:4422304 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1018-262G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 4/14 | chr19 | 4422304 | |||||||
chr19:4423081 | G | T | 1 | a0001c0007t0001g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1248-254G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 5/14 | chr19 | 4423081 | |||||||
chr19:4423422 | C | T | 36 | a0001c0003t0003g0011 a0001c0003t0003g0012 a0001c0003t0003g0013 others(33): Show |
39 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1308+27C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 6/14 | chr19 | 4423422 | |||||||
chr19:4423513 | C | T | 1 | a0002c0002t0002g0023 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1308+118C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 6/14 | chr19 | 4423513 | |||||||
chr19:4423602 | G | A | 2 | a0001c0003t0003g0319 a0001c0003t0003g0320 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1309-204G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 6/14 | chr19 | 4423602 | |||||||
chr19:4423768 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0264 |
3 | HG01261.hp2 HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1309-38C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 6/14 | chr19 | 4423768 | |||||||
chr19:4424132 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1377+258G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424132 | |||||||
chr19:4424249 | G | A | 1 | a0004c0005t0002g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1377+375G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424249 | |||||||
chr19:4424299 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1377+425A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424299 | |||||||
chr19:4424459 | T | C | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377+585T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424459 | |||||||
chr19:4424557 | A | G | 8 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(5): Show |
8 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377+683A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424557 | |||||||
chr19:4424583 | C | T | 11 | a0002c0002t0002g0355 a0002c0012t0002g0365 a0005c0006t0002g0356 others(8): Show |
11 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1377+709C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424583 | |||||||
chr19:4424618 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377+744C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424618 | |||||||
chr19:4424620 | A | G | 1 | a0013c0013t0002g0364 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1377+746A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424620 | |||||||
chr19:4424696 | G | A | 2 | a0002c0012t0002g0365 a0013c0013t0002g0364 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1377+822G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424696 | |||||||
chr19:4424807 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1377+933G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424807 | |||||||
chr19:4424903 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1377+1029G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424903 | |||||||
chr19:4424925 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1377+1051G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424925 | |||||||
chr19:4424993 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1377+1119C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4424993 | |||||||
chr19:4425027 | G | A | 1 | a0001c0003t0003g0305 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1377+1153G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425027 | |||||||
chr19:4425212 | T | C | 3 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0045 |
3 | HG00280.hp2 HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1377+1338T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425212 | |||||||
chr19:4425239 | C | CT | 56 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(53): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1377+1372dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4425239 | ||||||
chr19:4425268 | A | G | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1377+1394A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425268 | |||||||
chr19:4425308 | T | G | 56 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(53): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1377+1434T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425308 | |||||||
chr19:4425312 | G | A | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1377+1438G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425312 | |||||||
chr19:4425377 | C | T | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1377+1503C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425377 | |||||||
chr19:4425452 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1377+1578C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425452 | |||||||
chr19:4425539 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1377+1665G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425539 | |||||||
chr19:4425826 | T | C | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377+1952T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425826 | |||||||
chr19:4425838 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1377+1964G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425838 | |||||||
chr19:4425860 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1377+1986A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425860 | |||||||
chr19:4425998 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0163 |
2 | NA18960.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1377+2124G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4425998 | |||||||
chr19:4426115 | A | G | 107 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(104): Show |
113 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1377+2241A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426115 | |||||||
chr19:4426141 | C | G | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1377+2267C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426141 | |||||||
chr19:4426167 | CT | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
297 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.1377+2311delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4426167 | ||||||
chr19:4426310 | A | G | 1 | a0002c0002t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1378-2354A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426310 | |||||||
chr19:4426410 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1378-2254C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426410 | |||||||
chr19:4426414 | C | T | 3 | a0003c0004t0002g0338 a0003c0004t0002g0339 a0003c0004t0002g0342 |
3 | HG02922.hp1 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1378-2250C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426414 | |||||||
chr19:4426419 | C | T | 1 | a0001c0003t0008g0312 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1378-2245C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426419 | |||||||
chr19:4426459 | T | G | 5 | a0001c0003t0003g0278 a0001c0003t0003g0279 a0001c0003t0003g0280 others(2): Show |
5 | HG02602.hp1 HG02698.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-2205T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426459 | |||||||
chr19:4426631 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1378-2033C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426631 | |||||||
chr19:4426768 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1378-1896C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426768 | |||||||
chr19:4426788 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1378-1876T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426788 | |||||||
chr19:4426810 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1378-1854G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426810 | |||||||
chr19:4426828 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1378-1836T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426828 | |||||||
chr19:4426871 | A | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1378-1793A>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4426871 | |||||||
chr19:4427112 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1378-1552T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427112 | |||||||
chr19:4427136 | C | CTTTTTTT others(2): Show |
34 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0146 others(31): Show |
36 | HG00733.hp1 HG01069.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1378-1505_1378-149 others(13): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(3): Show |
43 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0026 others(40): Show |
45 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1378-1506_1378-149 others(14): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(4): Show |
22 | a0001c0001t0001g0123 a0001c0001t0001g0142 a0001c0001t0001g0152 others(19): Show |
22 | HG01106.hp1 HG01243.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1378-1507_1378-149 others(15): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(5): Show |
12 | a0001c0001t0001g0121 a0001c0001t0001g0137 a0001c0001t0001g0172 others(9): Show |
12 | HG00438.hp2 HG02071.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378-1508_1378-149 others(16): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0001g0145 a0001c0001t0001g0150 a0001c0001t0001g0187 others(5): Show |
8 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378-1509_1378-149 others(17): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG02055.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1378-1510_1378-149 others(18): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0260 |
2 | HG04184.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1378-1511_1378-149 others(19): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1378-1512_1378-149 others(20): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(10): Show |
5 | a0001c0001t0001g0139 a0001c0001t0001g0188 a0001c0001t0001g0211 others(2): Show |
5 | HG01192.hp1 HG02056.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-1513_1378-149 others(21): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(11): Show |
2 | a0003c0004t0002g0340 a0003c0004t0002g0344 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1378-1514_1378-149 others(22): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0010 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-1518_1378-149 others(26): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0246 a0001c0001t0001g0254 |
3 | HG02280.hp2 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1378-1519_1378-149 others(27): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1378-1520_1378-149 others(28): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(18): Show |
4 | a0001c0001t0001g0122 a0001c0001t0001g0239 a0001c0001t0001g0252 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-1521_1378-149 others(29): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1378-1522_1378-149 others(30): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1378-1523_1378-149 others(31): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1378-1525_1378-149 others(33): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | C | CTTTTTTT others(24): Show |
1 | a0003c0004t0002g0338 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1378-1527_1378-149 others(35): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CT | C | 7 | a0001c0001t0001g0192 a0004c0005t0002g0348 a0004c0005t0002g0349 others(4): Show |
7 | HG02080.hp1 HG02683.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1378-1497delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTT | C | 11 | a0001c0001t0001g0159 a0001c0001t0003g0326 a0001c0001t0003g0328 others(8): Show |
11 | HG00621.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1378-1499_1378-149 others(7): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTT | C | 48 | a0001c0001t0001g0222 a0001c0001t0001g0250 a0001c0001t0003g0323 others(45): Show |
51 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1378-1500_1378-149 others(8): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTT | C | 14 | a0002c0002t0002g0018 a0002c0002t0002g0030 a0002c0002t0002g0032 others(11): Show |
14 | HG00621.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378-1501_1378-149 others(9): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTTT | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(86): Show |
95 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1378-1502_1378-149 others(10): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTTTT | C | 17 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0131 others(14): Show |
17 | HG00423.hp2 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1378-1503_1378-149 others(11): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0132 others(5): Show |
8 | HG00544.hp2 HG02132.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378-1504_1378-149 others(12): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTTTT others(3): Show |
C | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1378-1506_1378-149 others(14): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1378-1507_1378-149 others(15): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427136 | CTTTTTTT others(12): Show |
C | 3 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0088 |
3 | HG03490.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1378-1515_1378-149 others(23): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427136 | ||||||
chr19:4427227 | G | A | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1378-1437G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427227 | |||||||
chr19:4427317 | TTTTTGTT others(3): Show |
T | 2 | a0001c0001t0001g0122 a0001c0003t0003g0293 |
2 | HG01243.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1378-1327_1378-131 others(14): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4427317 | ||||||
chr19:4427483 | G | A | 2 | a0001c0003t0003g0277 a0001c0003t0003g0296 |
2 | HG00099.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1378-1181G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427483 | |||||||
chr19:4427733 | G | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1378-931G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427733 | |||||||
chr19:4427743 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1378-921G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427743 | |||||||
chr19:4427834 | C | T | 4 | a0001c0007t0001g0124 a0001c0007t0001g0176 a0001c0007t0001g0190 others(1): Show |
4 | HG02559.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-830C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427834 | |||||||
chr19:4427853 | G | A | 1 | a0004c0005t0002g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1378-811G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427853 | |||||||
chr19:4427879 | C | T | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1378-785C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4427879 | |||||||
chr19:4428212 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1378-452G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428212 | |||||||
chr19:4428242 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1378-422T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428242 | |||||||
chr19:4428291 | CT | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
165 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1378-355delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 4428291 | ||||||
chr19:4428309 | T | A | 2 | a0002c0002t0002g0069 a0002c0002t0002g0070 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1378-355T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428309 | |||||||
chr19:4428381 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1378-283T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428381 | |||||||
chr19:4428480 | C | G | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1378-184C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428480 | |||||||
chr19:4428514 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0021t0001g0141 |
3 | NA18959.hp2 NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1378-150G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428514 | |||||||
chr19:4428602 | G | C | 1 | a0004c0005t0002g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1378-62G>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 7/14 | chr19 | 4428602 | |||||||
chr19:4428929 | T | C | 1 | a0003c0004t0002g0338 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1604+39T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 8/14 | chr19 | 4428929 | |||||||
chr19:4428963 | C | T | 1 | a0004c0005t0002g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1604+73C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 8/14 | chr19 | 4428963 | |||||||
chr19:4429010 | C | T | 47 | a0001c0003t0003g0011 a0001c0003t0003g0012 a0001c0003t0003g0013 others(44): Show |
50 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1604+120C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 8/14 | chr19 | 4429010 | |||||||
chr19:4429158 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(354): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1604+268T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 8/14 | chr19 | 4429158 | |||||||
chr19:4429932 | C | T | 2 | a0005c0018t0002g0363 a0009c0019t0002g0362 |
2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1854+144C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 10/14 | chr19 | 4429932 | |||||||
chr19:4430180 | ATT | A | 4 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG01256.hp2 HG02280.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855-363_1855-362d others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 4430180 | ||||||
chr19:4430246 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1855-303C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 10/14 | chr19 | 4430246 | |||||||
chr19:4430472 | C | T | 19 | a0001c0001t0001g0125 a0001c0001t0001g0166 a0001c0001t0001g0168 others(16): Show |
19 | HG00741.hp1 HG01074.hp1 HG02273.hp1 others(16): Show |
intron_variant | MODIFIER | c.1855-77C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 10/14 | chr19 | 4430472 | |||||||
chr19:4431067 | C | G | 1 | a0002c0002t0002g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1947+426C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431067 | |||||||
chr19:4431105 | A | G | 2 | a0002c0002t0002g0028 a0002c0002t0002g0093 |
2 | HG02056.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1947+464A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431105 | |||||||
chr19:4431144 | C | A | 2 | a0002c0012t0002g0365 a0013c0013t0002g0364 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1947+503C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431144 | |||||||
chr19:4431187 | G | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
9 | HG00423.hp2 HG00544.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1947+546G>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431187 | |||||||
chr19:4431209 | A | G | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1947+568A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431209 | |||||||
chr19:4431267 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0264 |
3 | HG01261.hp2 HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1947+626T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431267 | |||||||
chr19:4431282 | C | A | 1 | a0014c0016t0002g0075 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1947+641C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431282 | |||||||
chr19:4431353 | T | A | 1 | a0002c0002t0002g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1948-599T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431353 | |||||||
chr19:4431354 | C | A | 1 | a0002c0002t0002g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1948-598C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431354 | |||||||
chr19:4431484 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0225 a0001c0001t0001g0239 others(14): Show |
18 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1948-468G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431484 | |||||||
chr19:4431569 | C | T | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1948-383C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431569 | |||||||
chr19:4431784 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1948-168G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431784 | |||||||
chr19:4431793 | C | T | 2 | a0002c0012t0002g0365 a0013c0013t0002g0364 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1948-159C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431793 | |||||||
chr19:4431899 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(158): Show |
166 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1948-53C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 11/14 | chr19 | 4431899 | |||||||
chr19:4432358 | G | A | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2203+151G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432358 | |||||||
chr19:4432447 | T | C | 52 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(49): Show |
55 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.2203+240T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432447 | |||||||
chr19:4432611 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2203+404T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432611 | |||||||
chr19:4432758 | T | TAA | 207 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(204): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2204-298_2204-297d others(4): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 4432758 | ||||||
chr19:4432758 | T | TAAA | 10 | a0001c0001t0001g0121 a0001c0001t0001g0128 a0001c0001t0001g0139 others(7): Show |
10 | HG00597.hp2 HG01169.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.2204-299_2204-297d others(5): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 4432758 | ||||||
chr19:4432869 | C | T | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2204-201C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432869 | |||||||
chr19:4432915 | C | T | 1 | a0001c0007t0001g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2204-155C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432915 | |||||||
chr19:4432918 | T | A | 1 | a0004c0005t0002g0348 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2204-152T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432918 | |||||||
chr19:4432927 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0231 |
2 | HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2204-143C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432927 | |||||||
chr19:4432951 | C | T | 1 | a0002c0002t0002g0093 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2204-119C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432951 | |||||||
chr19:4432976 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2204-94G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4432976 | |||||||
chr19:4432999 | GTT | G | 3 | a0001c0007t0001g0176 a0001c0007t0001g0190 a0001c0007t0001g0204 |
3 | HG02559.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2204-68_2204-67del others(2): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 4432999 | ||||||
chr19:4433013 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2204-57C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4433013 | |||||||
chr19:4433029 | G | A | 8 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(5): Show |
8 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2204-41G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 12/14 | chr19 | 4433029 | |||||||
chr19:4433575 | G | T | 1 | a0001c0003t0008g0312 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2673+36G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4433575 | |||||||
chr19:4433617 | T | C | 1 | a0002c0002t0002g0001 | 3 | NA18980.hp1 NA19004.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2673+78T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4433617 | |||||||
chr19:4433895 | T | C | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2673+356T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4433895 | |||||||
chr19:4433897 | G | T | 1 | a0001c0003t0008g0312 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2673+358G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4433897 | |||||||
chr19:4434257 | G | A | 1 | a0001c0003t0003g0293 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2673+718G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434257 | |||||||
chr19:4434324 | C | T | 1 | a0015c0017t0002g0090 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2673+785C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434324 | |||||||
chr19:4434325 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2673+786G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434325 | |||||||
chr19:4434374 | G | A | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2673+835G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434374 | |||||||
chr19:4434467 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2673+928T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434467 | |||||||
chr19:4434506 | C | T | 52 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0326 others(49): Show |
55 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.2673+967C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434506 | |||||||
chr19:4434525 | T | C | 11 | a0001c0001t0001g0239 a0001c0001t0001g0244 a0001c0001t0001g0246 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2673+986T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434525 | |||||||
chr19:4434817 | C | T | 2 | a0002c0002t0002g0069 a0002c0002t0002g0070 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2673+1278C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434817 | |||||||
chr19:4434843 | C | T | 8 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(5): Show |
8 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2673+1304C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434843 | |||||||
chr19:4434892 | G | A | 2 | a0001c0001t0001g0231 a0005c0006t0002g0356 |
2 | HG02071.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2673+1353G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434892 | |||||||
chr19:4434953 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2673+1414C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4434953 | |||||||
chr19:4435005 | C | A | 2 | a0001c0003t0003g0294 a0001c0003t0003g0295 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2673+1466C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435005 | |||||||
chr19:4435087 | C | CT | 112 | a0001c0001t0003g0331 a0001c0003t0003g0290 a0001c0003t0003g0307 others(109): Show |
118 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.2673+1571dupT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4435087 | ||||||
chr19:4435087 | C | CTT | 15 | a0002c0002t0002g0058 a0002c0002t0002g0092 a0002c0002t0002g0103 others(12): Show |
15 | HG01496.hp1 HG01934.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2673+1570_2673+157 others(6): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4435087 | ||||||
chr19:4435087 | CT | C | 6 | a0001c0001t0001g0195 a0001c0001t0004g0327 a0001c0001t0010g0119 others(3): Show |
6 | HG01109.hp2 HG01256.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.2673+1571delT | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4435087 | ||||||
chr19:4435087 | CTT | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0001c0001t0001g0177 others(5): Show |
8 | HG01255.hp2 HG01952.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2673+1570_2673+157 others(6): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4435087 | ||||||
chr19:4435087 | CTTT | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
155 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.2673+1569_2673+157 others(7): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4435087 | ||||||
chr19:4435112 | A | T | 1 | a0001c0001t0001g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2673+1573A>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435112 | |||||||
chr19:4435133 | C | G | 1 | a0013c0013t0002g0364 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2673+1594C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435133 | |||||||
chr19:4435228 | C | G | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2673+1689C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435228 | |||||||
chr19:4435299 | C | T | 1 | a0001c0003t0003g0288 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2673+1760C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435299 | |||||||
chr19:4435324 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2673+1785C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435324 | |||||||
chr19:4435338 | A | G | 1 | a0002c0002t0002g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2673+1799A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435338 | |||||||
chr19:4435389 | T | C | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2673+1850T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435389 | |||||||
chr19:4435693 | T | C | 1 | a0001c0001t0010g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2673+2154T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435693 | |||||||
chr19:4435993 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG03834.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.2673+2454G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4435993 | |||||||
chr19:4436142 | A | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
179 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.2673+2603A>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436142 | |||||||
chr19:4436148 | AAAAG | A | 11 | a0002c0002t0002g0355 a0002c0012t0002g0365 a0005c0006t0002g0356 others(8): Show |
11 | HG01167.hp2 HG02818.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.2673+2613_2673+261 others(8): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4436148 | ||||||
chr19:4436324 | C | T | 1 | a0002c0002t0002g0053 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2673+2785C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436324 | |||||||
chr19:4436416 | C | T | 1 | a0001c0001t0010g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2673+2877C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436416 | |||||||
chr19:4436637 | G | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2673+3098G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436637 | |||||||
chr19:4436723 | C | T | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2673+3184C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436723 | |||||||
chr19:4436730 | C | A | 1 | a0001c0001t0010g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2673+3191C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436730 | |||||||
chr19:4436895 | CCACATCA others(36): Show |
C | 1 | a0010c0015t0003g0291 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2673+3357_2673+339 others(47): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4436895 | |||||||
chr19:4437082 | G | T | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2673+3543G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437082 | |||||||
chr19:4437092 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2673+3553C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437092 | |||||||
chr19:4437103 | T | C | 1 | a0001c0003t0009g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2673+3564T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437103 | |||||||
chr19:4437117 | G | A | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2673+3578G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437117 | |||||||
chr19:4437132 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2673+3593C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437132 | |||||||
chr19:4437159 | A | AAT | 14 | a0002c0023t0002g0366 a0003c0004t0002g0332 a0003c0004t0002g0334 others(11): Show |
14 | HG01109.hp2 HG02109.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2673+3621_2673+362 others(6): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4437159 | ||||||
chr19:4437159 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2673+3620A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437159 | |||||||
chr19:4437453 | A | G | 60 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 others(57): Show |
63 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2673+3914A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437453 | |||||||
chr19:4437510 | C | T | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2673+3971C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437510 | |||||||
chr19:4437524 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
10 | HG02074.hp1 HG02083.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.2673+3985A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437524 | |||||||
chr19:4437547 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2673+4008A>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437547 | |||||||
chr19:4437735 | T | TTTTTA | 352 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(349): Show |
366 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.2673+4216_2673+422 others(9): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4437735 | ||||||
chr19:4437735 | T | TTTTTATT others(3): Show |
2 | a0001c0003t0003g0284 a0001c0003t0003g0285 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2673+4211_2673+422 others(14): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4437735 | ||||||
chr19:4437735 | T | TTTTTATT others(8): Show |
2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2673+4206_2673+422 others(19): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4437735 | ||||||
chr19:4437763 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
136 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.2673+4224G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437763 | |||||||
chr19:4437862 | C | T | 1 | a0002c0002t0002g0095 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2673+4323C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437862 | |||||||
chr19:4437885 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2673+4346G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437885 | |||||||
chr19:4437889 | A | G | 1 | a0006c0008t0003g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2673+4350A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437889 | |||||||
chr19:4437898 | C | A | 1 | a0006c0008t0003g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2674-4347C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437898 | |||||||
chr19:4437915 | A | G | 2 | a0001c0003t0003g0309 a0001c0003t0007g0313 |
2 | HG00544.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2674-4330A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437915 | |||||||
chr19:4437917 | T | A | 2 | a0001c0003t0003g0309 a0001c0003t0007g0313 |
2 | HG00544.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2674-4328T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437917 | |||||||
chr19:4437976 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2674-4269T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437976 | |||||||
chr19:4437992 | C | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(249): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2674-4253C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4437992 | |||||||
chr19:4438009 | A | G | 5 | a0005c0006t0002g0356 a0005c0006t0002g0357 a0005c0006t0002g0358 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2674-4236A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438009 | |||||||
chr19:4438026 | A | C | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2674-4219A>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438026 | |||||||
chr19:4438031 | A | G | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2674-4214A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438031 | |||||||
chr19:4438086 | C | A | 1 | a0002c0002t0002g0100 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2674-4159C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438086 | |||||||
chr19:4438354 | T | TTTTTG | 111 | a0001c0001t0001g0238 a0001c0001t0001g0256 a0001c0001t0001g0258 others(108): Show |
117 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.2674-3869_2674-386 others(9): Show |
CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4438354 | ||||||
chr19:4438408 | G | A | 1 | a0002c0023t0002g0366 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2674-3837G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438408 | |||||||
chr19:4438939 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2674-3306G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438939 | |||||||
chr19:4438975 | C | T | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2674-3270C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4438975 | |||||||
chr19:4439094 | C | G | 4 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG01256.hp2 HG02280.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2674-3151C>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439094 | |||||||
chr19:4439123 | T | C | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2674-3122T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439123 | |||||||
chr19:4439391 | G | A | 14 | a0001c0003t0003g0012 a0001c0003t0003g0278 a0001c0003t0003g0279 others(11): Show |
15 | HG00280.hp1 HG00639.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2674-2854G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439391 | |||||||
chr19:4439528 | G | A | 107 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(104): Show |
113 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2674-2717G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439528 | |||||||
chr19:4439571 | C | T | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2674-2674C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439571 | |||||||
chr19:4439574 | C | T | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2674-2671C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439574 | |||||||
chr19:4439577 | G | A | 1 | a0002c0011t0002g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2674-2668G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439577 | |||||||
chr19:4439658 | C | T | 1 | a0001c0001t0010g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2674-2587C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439658 | |||||||
chr19:4439697 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2674-2548A>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439697 | |||||||
chr19:4439728 | A | G | 107 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(104): Show |
113 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2674-2517A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4439728 | |||||||
chr19:4440267 | G | A | 4 | a0002c0002t0002g0074 a0002c0002t0002g0079 a0002c0002t0002g0082 others(1): Show |
4 | HG02647.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2674-1978G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440267 | |||||||
chr19:4440311 | A | G | 1 | a0007c0010t0006g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2674-1934A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440311 | |||||||
chr19:4440371 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2674-1874G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440371 | |||||||
chr19:4440610 | A | G | 2 | a0007c0010t0006g0367 a0007c0010t0006g0368 |
2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2674-1635A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440610 | |||||||
chr19:4440615 | G | T | 1 | a0002c0002t0002g0043 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2674-1630G>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440615 | |||||||
chr19:4440654 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2674-1591T>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440654 | |||||||
chr19:4440732 | G | A | 1 | a0001c0003t0003g0298 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2674-1513G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4440732 | |||||||
chr19:4440999 | T | TA | 8 | a0002c0002t0002g0015 a0002c0002t0002g0024 a0002c0002t0002g0099 others(5): Show |
8 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.2674-1231dupA | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4440999 | ||||||
chr19:4440999 | TA | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(161): Show |
169 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2674-1231delA | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 4440999 | ||||||
chr19:4441055 | C | T | 2 | a0001c0003t0003g0292 a0001c0003t0003g0293 |
2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2674-1190C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441055 | |||||||
chr19:4441086 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2674-1159G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441086 | |||||||
chr19:4441217 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0212 |
2 | HG01943.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2674-1028C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441217 | |||||||
chr19:4441285 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0153 |
3 | HG02074.hp1 HG02132.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2674-960C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441285 | |||||||
chr19:4441318 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(210): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2674-927G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441318 | |||||||
chr19:4441375 | T | C | 1 | a0004c0005t0002g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2674-870T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441375 | |||||||
chr19:4441410 | C | T | 57 | a0001c0001t0001g0158 a0001c0001t0003g0323 a0001c0001t0003g0324 others(54): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2674-835C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441410 | |||||||
chr19:4441515 | C | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0173 a0001c0001t0001g0268 others(1): Show |
4 | HG02027.hp2 NA18985.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2674-730C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441515 | |||||||
chr19:4441603 | C | A | 1 | a0002c0002t0002g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2674-642C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441603 | |||||||
chr19:4441675 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(220): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2674-570G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441675 | |||||||
chr19:4441719 | C | A | 1 | a0011c0025t0002g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2674-526C>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441719 | |||||||
chr19:4441766 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2674-479C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441766 | |||||||
chr19:4441790 | C | T | 1 | a0001c0003t0003g0013 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2674-455C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441790 | |||||||
chr19:4441823 | G | A | 12 | a0003c0004t0002g0332 a0003c0004t0002g0334 a0003c0004t0002g0335 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2674-422G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441823 | |||||||
chr19:4441916 | A | G | 4 | a0002c0002t0002g0074 a0002c0002t0002g0079 a0002c0002t0002g0082 others(1): Show |
4 | HG02647.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2674-329A>G | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441916 | |||||||
chr19:4441957 | C | T | 109 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2674-288C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 13/14 | chr19 | 4441957 | |||||||
chr19:4442495 | G | A | 2 | a0001c0003t0003g0319 a0001c0003t0003g0320 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2770+154G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442495 | |||||||
chr19:4442532 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2770+191T>C | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442532 | |||||||
chr19:4442534 | G | A | 1 | a0002c0002t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2770+193G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442534 | |||||||
chr19:4442635 | C | T | 1 | a0005c0006t0002g0360 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2771-290C>T | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442635 | |||||||
chr19:4442637 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2771-288G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442637 | |||||||
chr19:4442700 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2771-225G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442700 | |||||||
chr19:4442814 | G | A | 3 | a0001c0003t0003g0012 a0001c0003t0003g0284 a0001c0003t0003g0285 |
4 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2771-111G>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442814 | |||||||
chr19:4442866 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2771-59T>A | CHAF1A | ENSG00000167670.16 | transcript | ENST00000301280.10 | protein_coding | 14/14 | chr19 | 4442866 |