Item | Value |
---|---|
geneid | 91408 |
ensemblid | ENSG00000134717.18 |
hgncid | 30547 |
symbol | BTF3L4 |
name | basic transcription factor 3 like 4 |
refseq_nuc | NM_152265.5 |
refseq_prot | NP_689478.1 |
ensembl_nuc | ENST00000313334.13 |
ensembl_prot | ENSP00000360664.4 |
mane_status | MANE Select |
chr | chr1 |
start | 52056295 |
end | 52090716 |
strand | + |
ver | v1.2 |
region | chr1:52056295-52090716 |
region5000 | chr1:52051295-52095716 |
regionname0 | BTF3L4_chr1_52056295_52090716 |
regionname5000 | BTF3L4_chr1_52051295_52095716 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 474 | 276 | 92 | 48 | 94 | 10 | 30 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | ATGAA others(469): Show |
chr1 | 52051295 | 52095716 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4533 | 116 | 16 | 31 | 41 | 9 | 19 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0002 | 0/1 | 4534 | 27 | 12 | 1 | 9 | 0 | 4 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4529): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0003 | 0/0 | 4535 | 25 | 24 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0004 | 0/0 | 4535 | 22 | 0 | 4 | 18 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0005 | 0/0 | 4533 | 10 | 0 | 0 | 8 | 0 | 2 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0006 | 0/0 | 4535 | 10 | 8 | 1 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0007 | 1/0 | 4533 | 7 | 5 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0008 | 0/0 | 4537 | 6 | 5 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4532): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0009 | 0/0 | 4536 | 5 | 0 | 0 | 5 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4531): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0010 | 0/0 | 4533 | 5 | 0 | 0 | 5 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0011 | 0/0 | 4535 | 4 | 4 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0012 | 0/0 | 4536 | 4 | 2 | 2 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4531): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0013 | 0/0 | 4534 | 3 | 2 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4529): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0014 | 0/0 | 4536 | 3 | 0 | 1 | 0 | 1 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4531): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0015 | 0/0 | 4533 | 2 | 0 | 2 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0016 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0017 | 0/0 | 4533 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0018 | 0/0 | 4534 | 2 | 2 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4529): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0019 | 0/0 | 4534 | 2 | 2 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4529): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0020 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0021 | 0/0 | 4534 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4529): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0022 | 0/0 | 4535 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0023 | 0/0 | 4535 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0024 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0025 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0026 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0027 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0028 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0029 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0030 | 0/0 | 4534 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4529): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0031 | 0/0 | 4535 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4530): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0032 | 0/0 | 4536 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4531): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0033 | 0/0 | 4537 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4532): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0034 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0035 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0036 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
a0001c0001t0037 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | GCCGC others(4528): Show |
chr1 | 52051295 | 52095716 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0007g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0012g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0012g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0013g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0014g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0014g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0015g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0015g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0017g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0017g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0018g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0019g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0020g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0021g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0022g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0024g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0025g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0026g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0027g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0028g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0029g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0030g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0031g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0032g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0033g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0034g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0035g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0036g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
a0001c0001t0037g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00099 | hp2 | a0001 | c0001 | t0014 | g0226 | EUR | GBR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00544 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0253 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00609 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00639 | hp2 | a0001 | c0001 | t0008 | g0077 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0098 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00673 | hp2 | a0001 | c0001 | t0010 | g0106 | EAS | CHS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01074 | hp2 | a0001 | c0001 | t0035 | g0138 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01167 | hp1 | a0001 | c0001 | t0012 | g0043 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0160 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01169 | hp1 | a0001 | c0001 | t0015 | g0233 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01175 | hp1 | a0001 | c0001 | t0012 | g0036 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01175 | hp2 | a0001 | c0001 | t0014 | g0227 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01243 | hp2 | a0001 | c0001 | t0013 | g0177 | AMR | PUR | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0168 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01934 | hp2 | a0001 | c0001 | t0027 | g0148 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01943 | hp1 | a0001 | c0001 | t0034 | g0210 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0071 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02132 | hp2 | a0001 | c0001 | t0009 | g0054 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02135 | hp1 | a0001 | c0001 | t0009 | g0053 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0033 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0200 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0235 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0060 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0222 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02717 | hp2 | a0001 | c0001 | t0032 | g0081 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02735 | hp2 | a0001 | c0001 | t0014 | g0221 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0061 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02965 | hp1 | a0001 | c0001 | t0024 | g0112 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02965 | hp2 | a0001 | c0001 | t0031 | g0244 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0239 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0078 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0240 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0072 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0062 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03139 | hp1 | a0001 | c0001 | t0013 | g0169 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03225 | hp1 | a0001 | c0001 | t0018 | g0234 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03486 | hp2 | a0001 | c0001 | t0033 | g0076 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | ESN | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03579 | hp2 | a0001 | c0001 | t0036 | g0131 | AFR | MSL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0248 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG04115 | hp2 | a0001 | c0001 | t0030 | g0246 | SAS | STU | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG04204 | hp1 | a0001 | c0001 | t0028 | g0232 | SAS | STU | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | STU | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | YRI | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18522 | hp2 | a0001 | c0001 | t0019 | g0092 | AFR | YRI | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | CHB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18906 | hp1 | a0001 | c0001 | t0029 | g0122 | AFR | YRI | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | YRI | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18942 | hp2 | a0001 | c0001 | t0017 | g0157 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18959 | hp2 | a0001 | c0001 | t0010 | g0102 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18966 | hp2 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18980 | hp2 | a0001 | c0001 | t0025 | g0202 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18985 | hp2 | a0001 | c0001 | t0022 | g0069 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19005 | hp1 | a0001 | c0001 | t0026 | g0152 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | LWK | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19054 | hp1 | a0001 | c0001 | t0021 | g0055 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19063 | hp1 | a0001 | c0001 | t0010 | g0108 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19064 | hp1 | a0001 | c0001 | t0017 | g0139 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19082 | hp2 | a0001 | c0001 | t0023 | g0005 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19084 | hp1 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19090 | hp1 | a0001 | c0001 | t0037 | g0104 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19240 | hp1 | a0001 | c0001 | t0019 | g0093 | AFR | YRI | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | YRI | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA20129 | hp1 | a0001 | c0001 | t0020 | g0199 | AFR | ASW | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ASW | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | GIH | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | GIH | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0241 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | ACB | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | USA | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | USA | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | USA | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0075 | AFR | USA | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0194 | REF | REF | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0068 | REF | REF | BTF3L4_chr1_52051295_52095716 | BTF3L4 | chr1 | 52051295 | 52095716 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52086965 | T | C | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0021 others(2): Show |
30 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*207T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 207 | chr1 | 52086965 | ||||||
chr1:52087056 | T | C | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 298 | chr1 | 52087056 | ||||||
chr1:52087073 | G | C | 1 | a0001c0001t0025 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 315 | chr1 | 52087073 | ||||||
chr1:52087086 | G | A | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(5): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*328G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 328 | chr1 | 52087086 | ||||||
chr1:52087091 | G | C | 1 | a0001c0001t0026 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 333 | chr1 | 52087091 | ||||||
chr1:52087273 | C | G | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(5): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*515C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 515 | chr1 | 52087273 | ||||||
chr1:52087408 | A | G | 1 | a0001c0001t0037 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 650 | chr1 | 52087408 | ||||||
chr1:52087451 | C | T | 1 | a0001c0001t0036 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 693 | chr1 | 52087451 | ||||||
chr1:52087580 | C | T | 1 | a0001c0001t0035 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 822 | chr1 | 52087580 | ||||||
chr1:52087724 | A | G | 1 | a0001c0001t0020 | 2 | HG02258.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*966A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 966 | chr1 | 52087724 | ||||||
chr1:52088079 | T | G | 1 | a0001c0001t0020 | 2 | HG02258.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1321T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 1321 | chr1 | 52088079 | ||||||
chr1:52088135 | A | G | 1 | a0001c0001t0034 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 1377 | chr1 | 52088135 | ||||||
chr1:52088527 | A | G | 1 | a0001c0001t0010 | 5 | HG00609.hp2 HG00673.hp2 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1769A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 1769 | chr1 | 52088527 | ||||||
chr1:52088913 | A | AT | 6 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0018 others(3): Show |
35 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2173dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2174 | INFO_REALIGN_3_PRIME | chr1 | 52088913 | |||||
chr1:52088913 | A | ATT | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(4): Show |
64 | HG00423.hp1 HG00609.hp1 HG00642.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2172_*2173dupTT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2174 | INFO_REALIGN_3_PRIME | chr1 | 52088913 | |||||
chr1:52088913 | A | ATTT | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0014 others(1): Show |
13 | HG00099.hp2 HG00544.hp1 HG01167.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2171_*2173dupTTT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2174 | INFO_REALIGN_3_PRIME | chr1 | 52088913 | |||||
chr1:52088913 | A | ATTTT | 2 | a0001c0001t0008 a0001c0001t0033 |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2170_*2173dupTTTT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2174 | INFO_REALIGN_3_PRIME | chr1 | 52088913 | |||||
chr1:52088973 | C | T | 1 | a0001c0001t0023 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2215C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2215 | chr1 | 52088973 | ||||||
chr1:52089158 | A | T | 1 | a0001c0001t0022 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2400 | chr1 | 52089158 | ||||||
chr1:52089247 | T | C | 2 | a0001c0001t0005 a0001c0001t0030 |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2489T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2489 | chr1 | 52089247 | ||||||
chr1:52089303 | C | T | 1 | a0001c0001t0017 | 2 | NA18942.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2545C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2545 | chr1 | 52089303 | ||||||
chr1:52089313 | T | A | 1 | a0001c0001t0031 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2555T>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2555 | chr1 | 52089313 | ||||||
chr1:52089450 | G | A | 1 | a0001c0001t0013 | 3 | HG01243.hp2 HG01884.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2692G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2692 | chr1 | 52089450 | ||||||
chr1:52089469 | T | G | 1 | a0001c0001t0015 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2711T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2711 | chr1 | 52089469 | ||||||
chr1:52089716 | C | T | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*2958C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 2958 | chr1 | 52089716 | ||||||
chr1:52089921 | C | G | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(31): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*3163C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3163 | chr1 | 52089921 | ||||||
chr1:52090021 | G | A | 2 | a0001c0001t0008 a0001c0001t0033 |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3263G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3263 | chr1 | 52090021 | ||||||
chr1:52090062 | A | G | 1 | a0001c0001t0019 | 2 | NA18522.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3304A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3304 | chr1 | 52090062 | ||||||
chr1:52090199 | C | T | 1 | a0001c0001t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3441C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3441 | chr1 | 52090199 | ||||||
chr1:52090313 | C | T | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(5): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3555C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3555 | chr1 | 52090313 | ||||||
chr1:52090314 | G | C | 1 | a0001c0001t0027 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3556 | chr1 | 52090314 | ||||||
chr1:52090319 | A | G | 2 | a0001c0001t0005 a0001c0001t0030 |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3561A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3561 | chr1 | 52090319 | ||||||
chr1:52090343 | T | A | 1 | a0001c0001t0016 | 2 | HG02055.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3585T>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3585 | chr1 | 52090343 | ||||||
chr1:52090412 | C | T | 1 | a0001c0001t0011 | 4 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3654C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3654 | chr1 | 52090412 | ||||||
chr1:52090550 | G | A | 1 | a0001c0001t0032 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3792G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3792 | chr1 | 52090550 | ||||||
chr1:52090558 | A | G | 1 | a0001c0001t0028 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3800A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3800 | chr1 | 52090558 | ||||||
chr1:52090630 | G | A | 1 | a0001c0001t0033 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3872G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 6/6 | 3872 | chr1 | 52090630 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:52056483 | T | A | 1 | a0001c0001t0006g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-14+104T>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056483 | |||||||
chr1:52056502 | C | G | 4 | a0001c0001t0002g0257 a0001c0001t0002g0258 a0001c0001t0002g0259 others(1): Show |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+123C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056502 | |||||||
chr1:52056572 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-14+193G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056572 | |||||||
chr1:52056587 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14+208C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056587 | |||||||
chr1:52056643 | A | T | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14+264A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056643 | |||||||
chr1:52056684 | C | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-14+305C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056684 | |||||||
chr1:52056690 | A | G | 1 | a0001c0001t0031g0244 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-14+311A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056690 | |||||||
chr1:52056692 | C | T | 1 | a0001c0001t0022g0069 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-14+313C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056692 | |||||||
chr1:52056796 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+417G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056796 | |||||||
chr1:52056800 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01168.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-14+421A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056800 | |||||||
chr1:52056818 | A | G | 202 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-14+439A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056818 | |||||||
chr1:52056844 | G | A | 256 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-14+465G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056844 | |||||||
chr1:52056854 | A | G | 4 | a0001c0001t0007g0015 a0001c0001t0007g0239 a0001c0001t0007g0240 others(1): Show |
5 | HG02486.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+475A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056854 | |||||||
chr1:52056889 | C | G | 4 | a0001c0001t0007g0015 a0001c0001t0007g0239 a0001c0001t0007g0240 others(1): Show |
5 | HG02486.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+510C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52056889 | |||||||
chr1:52057541 | G | A | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-14+1162G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52057541 | |||||||
chr1:52057659 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-14+1280G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52057659 | |||||||
chr1:52057888 | G | A | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+1509G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52057888 | |||||||
chr1:52057944 | CTGTT | C | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+1566_-14+1569d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52057944 | |||||||
chr1:52058242 | A | G | 1 | a0001c0001t0008g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-13-1593A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058242 | |||||||
chr1:52058409 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-13-1426A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058409 | |||||||
chr1:52058436 | C | G | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-13-1399C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058436 | |||||||
chr1:52058437 | T | C | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-13-1398T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058437 | |||||||
chr1:52058501 | G | A | 1 | a0001c0001t0008g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-13-1334G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058501 | |||||||
chr1:52058528 | T | G | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-13-1307T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058528 | |||||||
chr1:52058623 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0011g0059 a0001c0001t0011g0060 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1212C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058623 | |||||||
chr1:52058679 | G | A | 20 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(17): Show |
21 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13-1156G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058679 | |||||||
chr1:52058709 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-13-1126C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058709 | |||||||
chr1:52058749 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-13-1086G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058749 | |||||||
chr1:52058819 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13-1016C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058819 | |||||||
chr1:52058844 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-13-991T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058844 | |||||||
chr1:52058846 | C | T | 20 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(17): Show |
21 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13-989C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058846 | |||||||
chr1:52058962 | TG | T | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-872delG | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52058962 | |||||||
chr1:52059036 | A | G | 1 | a0001c0001t0005g0255 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-13-799A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059036 | |||||||
chr1:52059054 | G | T | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-781G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059054 | |||||||
chr1:52059061 | G | C | 1 | a0001c0001t0012g0036 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13-774G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059061 | |||||||
chr1:52059074 | G | GC | 23 | a0001c0001t0001g0014 a0001c0001t0003g0034 a0001c0001t0003g0035 others(20): Show |
24 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13-752dupC | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 52059074 | ||||||
chr1:52059180 | A | G | 1 | a0001c0001t0008g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-655A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059180 | |||||||
chr1:52059252 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-13-583C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059252 | |||||||
chr1:52059470 | A | G | 1 | a0001c0001t0018g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-13-365A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059470 | |||||||
chr1:52059489 | A | G | 1 | a0001c0001t0004g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-13-346A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059489 | |||||||
chr1:52059612 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13-223T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059612 | |||||||
chr1:52059693 | T | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG02080.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-13-142T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 1/5 | chr1 | 52059693 | |||||||
chr1:52059965 | G | A | 16 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0096 others(13): Show |
16 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.54+64G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52059965 | |||||||
chr1:52060187 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0101 others(9): Show |
13 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.54+286T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52060187 | |||||||
chr1:52060344 | C | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0230 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.54+443C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52060344 | |||||||
chr1:52060669 | A | T | 1 | a0001c0001t0007g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.54+768A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52060669 | |||||||
chr1:52060683 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.54+782A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52060683 | |||||||
chr1:52060914 | A | G | 14 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.54+1013A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52060914 | |||||||
chr1:52061000 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54+1099G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061000 | |||||||
chr1:52061077 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.54+1176C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061077 | |||||||
chr1:52061246 | C | T | 1 | a0001c0001t0006g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54+1345C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061246 | |||||||
chr1:52061363 | G | A | 1 | a0001c0001t0008g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.54+1462G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061363 | |||||||
chr1:52061398 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.54+1497G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061398 | |||||||
chr1:52061438 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.54+1537A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061438 | |||||||
chr1:52061487 | C | CA | 30 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0256 others(27): Show |
30 | HG00642.hp2 HG01074.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.54+1605dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52061487 | ||||||
chr1:52061503 | A | G | 10 | a0001c0001t0005g0247 a0001c0001t0005g0248 a0001c0001t0005g0249 others(7): Show |
10 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1602A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061503 | |||||||
chr1:52061630 | C | T | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.54+1729C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061630 | |||||||
chr1:52061635 | C | CT | 5 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0032 others(2): Show |
5 | HG00609.hp1 HG01891.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1756dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52061635 | ||||||
chr1:52061635 | CT | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0111 others(81): Show |
87 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.54+1756delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52061635 | ||||||
chr1:52061635 | CTT | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
125 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.54+1755_54+1756del others(2): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52061635 | ||||||
chr1:52061635 | CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0004g0003 a0001c0001t0004g0037 a0001c0001t0004g0038 others(4): Show |
8 | HG00423.hp1 HG01928.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+1745_54+1756del others(12): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52061635 | ||||||
chr1:52061680 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.54+1779G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061680 | |||||||
chr1:52061843 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.54+1942T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061843 | |||||||
chr1:52061943 | C | CT | 9 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
9 | HG00099.hp2 HG01175.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+2053dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52061943 | ||||||
chr1:52061990 | G | T | 1 | a0001c0001t0005g0254 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.54+2089G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52061990 | |||||||
chr1:52062156 | G | A | 256 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.54+2255G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062156 | |||||||
chr1:52062197 | C | CT | 7 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0001t0003g0032 others(4): Show |
7 | HG02257.hp1 HG02572.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+2318dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52062197 | ||||||
chr1:52062197 | CT | C | 174 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.54+2318delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 52062197 | ||||||
chr1:52062260 | G | A | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.54+2359G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062260 | |||||||
chr1:52062316 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.54+2415C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062316 | |||||||
chr1:52062446 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.55-2379C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062446 | |||||||
chr1:52062504 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.55-2321C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062504 | |||||||
chr1:52062744 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.55-2081C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062744 | |||||||
chr1:52062937 | C | CAG | 221 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(218): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.55-1888_55-1887ins others(2): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062937 | |||||||
chr1:52062951 | A | G | 3 | a0001c0001t0006g0016 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02109.hp1 HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.55-1874A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062951 | |||||||
chr1:52062970 | G | A | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.55-1855G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52062970 | |||||||
chr1:52063509 | G | T | 1 | a0001c0001t0004g0040 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.55-1316G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52063509 | |||||||
chr1:52063850 | A | G | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-975A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52063850 | |||||||
chr1:52063932 | A | G | 1 | a0001c0001t0012g0043 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.55-893A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52063932 | |||||||
chr1:52063966 | C | T | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-859C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52063966 | |||||||
chr1:52064091 | C | T | 4 | a0001c0001t0002g0257 a0001c0001t0002g0258 a0001c0001t0002g0259 others(1): Show |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-734C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52064091 | |||||||
chr1:52064260 | T | G | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.55-565T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52064260 | |||||||
chr1:52064590 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.55-235A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52064590 | |||||||
chr1:52064628 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01361.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.55-197G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52064628 | |||||||
chr1:52064651 | G | A | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.55-174G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52064651 | |||||||
chr1:52064750 | G | C | 1 | a0001c0001t0018g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.55-75G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 2/5 | chr1 | 52064750 | |||||||
chr1:52064969 | G | A | 3 | a0001c0001t0013g0168 a0001c0001t0013g0169 a0001c0001t0013g0177 |
3 | HG01243.hp2 HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.168+31G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52064969 | |||||||
chr1:52065064 | CTG | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0113 others(15): Show |
20 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+129_168+130del others(2): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52065064 | ||||||
chr1:52065085 | A | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(24): Show |
30 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.168+147A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065085 | |||||||
chr1:52065244 | A | G | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.168+306A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065244 | |||||||
chr1:52065358 | C | T | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.168+420C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065358 | |||||||
chr1:52065359 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.168+421G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065359 | |||||||
chr1:52065412 | C | T | 2 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+474C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065412 | |||||||
chr1:52065422 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+484T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065422 | |||||||
chr1:52065618 | C | A | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.168+680C>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065618 | |||||||
chr1:52065725 | T | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
7 | HG02080.hp1 HG02132.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+787T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065725 | |||||||
chr1:52065978 | C | T | 2 | a0001c0001t0003g0064 a0001c0001t0003g0066 |
2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.168+1040C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52065978 | |||||||
chr1:52066079 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.168+1141A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066079 | |||||||
chr1:52066214 | GA | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(24): Show |
30 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.168+1277delA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066214 | |||||||
chr1:52066267 | C | T | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.168+1329C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066267 | |||||||
chr1:52066320 | T | G | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1382T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066320 | |||||||
chr1:52066335 | G | A | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.168+1397G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066335 | |||||||
chr1:52066340 | C | T | 2 | a0001c0001t0014g0226 a0001c0001t0014g0227 |
2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.168+1402C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066340 | |||||||
chr1:52066358 | AT | A | 50 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(47): Show |
54 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.168+1435delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52066358 | ||||||
chr1:52066503 | G | A | 248 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(245): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.168+1565G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066503 | |||||||
chr1:52066565 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.168+1627C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066565 | |||||||
chr1:52066702 | C | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(24): Show |
30 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.168+1764C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066702 | |||||||
chr1:52066707 | A | G | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.168+1769A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066707 | |||||||
chr1:52066803 | G | A | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+1865G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066803 | |||||||
chr1:52066908 | A | G | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+1970A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066908 | |||||||
chr1:52066962 | C | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
90 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.168+2024C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52066962 | |||||||
chr1:52067461 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.168+2523G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52067461 | |||||||
chr1:52067584 | C | G | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+2646C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52067584 | |||||||
chr1:52067833 | G | A | 17 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(14): Show |
17 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+2895G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52067833 | |||||||
chr1:52068002 | G | GA | 200 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(197): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.168+3072dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52068002 | ||||||
chr1:52068134 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.168+3196G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068134 | |||||||
chr1:52068332 | A | T | 16 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0096 others(13): Show |
16 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+3394A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068332 | |||||||
chr1:52068528 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168+3590A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068528 | |||||||
chr1:52068553 | G | A | 1 | a0001c0001t0004g0044 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.168+3615G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068553 | |||||||
chr1:52068706 | G | A | 1 | a0001c0001t0012g0043 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.168+3768G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068706 | |||||||
chr1:52068731 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.168+3793A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068731 | |||||||
chr1:52068743 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.168+3805C>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068743 | |||||||
chr1:52068760 | G | A | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+3822G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068760 | |||||||
chr1:52068878 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.168+3940C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52068878 | |||||||
chr1:52069045 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.168+4107C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069045 | |||||||
chr1:52069116 | C | G | 3 | a0001c0001t0005g0251 a0001c0001t0005g0252 a0001c0001t0005g0255 |
3 | NA18969.hp1 NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.168+4178C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069116 | |||||||
chr1:52069177 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.168+4239A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069177 | |||||||
chr1:52069233 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168+4295A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069233 | |||||||
chr1:52069425 | T | C | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+4487T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069425 | |||||||
chr1:52069650 | A | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(24): Show |
30 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.168+4712A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069650 | |||||||
chr1:52069765 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.168+4827A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069765 | |||||||
chr1:52069795 | T | C | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+4857T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069795 | |||||||
chr1:52069795 | T | G | 1 | a0001c0001t0008g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168+4857T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069795 | |||||||
chr1:52069823 | G | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+4885G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069823 | |||||||
chr1:52069886 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.168+4948C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069886 | |||||||
chr1:52069911 | C | T | 3 | a0001c0001t0003g0042 a0001c0001t0012g0036 a0001c0001t0012g0043 |
3 | HG01167.hp1 HG01175.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.168+4973C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069911 | |||||||
chr1:52069943 | G | A | 1 | a0001c0001t0032g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.168+5005G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52069943 | |||||||
chr1:52070081 | G | A | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+5143G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52070081 | |||||||
chr1:52070127 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+5189G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52070127 | |||||||
chr1:52070196 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.168+5258G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52070196 | |||||||
chr1:52070213 | TA | T | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.168+5290delA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070213 | ||||||
chr1:52070299 | ATTGGTAT others(10): Show |
A | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+5397_168+5413d others(19): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070299 | ||||||
chr1:52070557 | C | CA | 132 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(129): Show |
140 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.168+5633dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070557 | ||||||
chr1:52070557 | C | CAA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0111 others(7): Show |
11 | HG00140.hp1 HG01074.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+5632_168+5633d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070557 | ||||||
chr1:52070633 | C | CT | 56 | a0001c0001t0002g0228 a0001c0001t0003g0002 a0001c0001t0003g0018 others(53): Show |
60 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.168+5712dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070633 | ||||||
chr1:52070633 | CT | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.168+5712delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070633 | ||||||
chr1:52070633 | CTTT | C | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+5710_168+5712d others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52070633 | ||||||
chr1:52070838 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.168+5900A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52070838 | |||||||
chr1:52070931 | G | A | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.168+5993G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52070931 | |||||||
chr1:52071107 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.168+6169A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071107 | |||||||
chr1:52071414 | T | C | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.168+6476T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071414 | |||||||
chr1:52071417 | A | T | 1 | a0001c0001t0003g0029 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.168+6479A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071417 | |||||||
chr1:52071607 | T | A | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.168+6669T>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071607 | |||||||
chr1:52071883 | T | C | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.168+6945T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071883 | |||||||
chr1:52071929 | C | CCCTG | 7 | a0001c0001t0004g0001 a0001c0001t0004g0041 a0001c0001t0004g0045 others(4): Show |
7 | HG00609.hp1 HG02004.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+6991_168+6992i others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071929 | |||||||
chr1:52071929 | C | CCCTGTG | 3 | a0001c0001t0004g0046 a0001c0001t0009g0001 a0001c0001t0009g0054 |
3 | HG00544.hp1 HG02071.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.168+6991_168+6992i others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071929 | |||||||
chr1:52071930 | T | C | 16 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(13): Show |
18 | HG00423.hp1 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.168+6992T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071930 | |||||||
chr1:52071931 | C | CTG | 25 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0174 others(22): Show |
25 | HG00642.hp1 HG01515.hp2 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.168+7035_168+7036d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | C | CTGTG | 25 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0135 others(22): Show |
25 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.168+7033_168+7036d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | C | CTGTGTG | 5 | a0001c0001t0001g0132 a0001c0001t0003g0065 a0001c0001t0005g0249 others(2): Show |
5 | HG00558.hp1 HG00735.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+7031_168+7036d others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | C | CTGTGTGT others(1): Show |
3 | a0001c0001t0003g0063 a0001c0001t0005g0250 a0001c0001t0005g0254 |
3 | HG00544.hp2 NA19082.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.168+7029_168+7036d others(10): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | C | G | 10 | a0001c0001t0004g0001 a0001c0001t0004g0041 a0001c0001t0004g0045 others(7): Show |
11 | HG00544.hp1 HG00609.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+6993C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071931 | |||||||
chr1:52071931 | CTG | C | 21 | a0001c0001t0001g0114 a0001c0001t0001g0158 a0001c0001t0001g0159 others(18): Show |
21 | HG00621.hp2 HG00673.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.168+7035_168+7036d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTG | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.168+7033_168+7036d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTGTG | C | 8 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00140.hp1 HG01074.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+7031_168+7036d others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTGTGT others(1): Show |
C | 18 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0142 others(15): Show |
19 | HG00099.hp2 HG01175.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+7029_168+7036d others(10): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0006g0082 a0001c0001t0018g0234 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.168+7027_168+7036d others(12): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTGTGT others(5): Show |
C | 3 | a0001c0001t0007g0084 a0001c0001t0018g0235 a0001c0001t0032g0081 |
3 | HG02145.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.168+7025_168+7036d others(14): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+7021_168+7036d others(18): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071931 | CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.168+7019_168+7036d others(20): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52071931 | ||||||
chr1:52071932 | T | C | 1 | a0001c0001t0009g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.168+6994T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071932 | |||||||
chr1:52071933 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.168+6995G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52071933 | |||||||
chr1:52072020 | G | GT | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.168+7091dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52072020 | ||||||
chr1:52072029 | T | TG | 13 | a0001c0001t0002g0216 a0001c0001t0002g0220 a0001c0001t0002g0223 others(10): Show |
13 | HG00099.hp2 HG01175.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+7092dupG | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52072029 | ||||||
chr1:52072030 | G | GT | 44 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(41): Show |
47 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+7104dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52072030 | ||||||
chr1:52072031 | T | G | 1 | a0001c0001t0002g0145 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.168+7093T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072031 | |||||||
chr1:52072043 | G | T | 1 | a0001c0001t0008g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168+7105G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072043 | |||||||
chr1:52072101 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168+7163C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072101 | |||||||
chr1:52072178 | C | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+7240C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072178 | |||||||
chr1:52072204 | G | A | 2 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+7266G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072204 | |||||||
chr1:52072416 | CATCTCTA others(8): Show |
C | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+7479_168+7493d others(17): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072416 | |||||||
chr1:52072508 | C | T | 17 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(14): Show |
17 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+7570C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072508 | |||||||
chr1:52072620 | A | G | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+7682A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072620 | |||||||
chr1:52072639 | G | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+7701G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072639 | |||||||
chr1:52072673 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168+7735A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072673 | |||||||
chr1:52072831 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0107 |
2 | NA18966.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.168+7893T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072831 | |||||||
chr1:52072960 | A | G | 9 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(6): Show |
10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+8022A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072960 | |||||||
chr1:52072977 | G | C | 9 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(6): Show |
10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+8039G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072977 | |||||||
chr1:52072990 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.168+8052G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52072990 | |||||||
chr1:52073073 | T | A | 3 | a0001c0001t0006g0016 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG02109.hp1 HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.168+8135T>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073073 | |||||||
chr1:52073083 | G | A | 14 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+8145G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073083 | |||||||
chr1:52073094 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.168+8156C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073094 | |||||||
chr1:52073305 | A | T | 14 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+8367A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073305 | |||||||
chr1:52073309 | C | A | 14 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+8371C>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073309 | |||||||
chr1:52073448 | A | ACACTATA others(6): Show |
18 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(15): Show |
21 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.168+8538_168+8550d others(15): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073448 | ||||||
chr1:52073488 | C | CACTATA | 9 | a0001c0001t0004g0005 a0001c0001t0004g0046 a0001c0001t0004g0047 others(6): Show |
9 | HG02027.hp2 HG02071.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+8550_168+8551i others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073488 | |||||||
chr1:52073491 | C | T | 9 | a0001c0001t0004g0005 a0001c0001t0004g0046 a0001c0001t0004g0047 others(6): Show |
9 | HG02027.hp2 HG02071.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+8553C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073491 | |||||||
chr1:52073492 | A | ATGC | 8 | a0001c0001t0004g0005 a0001c0001t0004g0046 a0001c0001t0004g0050 others(5): Show |
8 | HG02027.hp2 HG02071.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+8555_168+8556i others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073492 | ||||||
chr1:52073493 | T | TAC | 71 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(68): Show |
75 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.168+8591_168+8592d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | T | TACAC | 14 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0163 others(11): Show |
15 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+8589_168+8592d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | T | TACACAC | 6 | a0001c0001t0001g0196 a0001c0001t0001g0242 a0001c0001t0006g0016 others(3): Show |
6 | HG01168.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+8587_168+8592d others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0236 a0001c0001t0006g0094 a0001c0001t0006g0095 others(4): Show |
7 | HG00642.hp2 HG02735.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+8585_168+8592d others(10): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0089 a0001c0001t0002g0258 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.168+8583_168+8592d others(12): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | T | TACACACA others(5): Show |
5 | a0001c0001t0002g0096 a0001c0001t0002g0257 a0001c0001t0002g0259 others(2): Show |
5 | HG02622.hp1 HG02698.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+8581_168+8592d others(14): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | T | TACACACA others(9): Show |
1 | a0001c0001t0002g0088 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.168+8577_168+8592d others(18): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | TAC | T | 52 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
56 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.168+8591_168+8592d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | TACAC | T | 25 | a0001c0001t0002g0220 a0001c0001t0003g0002 a0001c0001t0003g0019 others(22): Show |
26 | HG01891.hp1 HG01943.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.168+8589_168+8592d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | TACACAC | T | 15 | a0001c0001t0003g0067 a0001c0001t0005g0245 a0001c0001t0005g0247 others(12): Show |
15 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+8587_168+8592d others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073493 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.168+8581_168+8592d others(14): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073493 | ||||||
chr1:52073495 | C | T | 1 | a0001c0001t0004g0047 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.168+8557C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073495 | |||||||
chr1:52073497 | C | T | 8 | a0001c0001t0004g0005 a0001c0001t0004g0046 a0001c0001t0004g0050 others(5): Show |
8 | HG02027.hp2 HG02071.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+8559C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073497 | |||||||
chr1:52073531 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.168+8593T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073531 | |||||||
chr1:52073558 | G | T | 1 | a0001c0001t0003g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.168+8620G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073558 | |||||||
chr1:52073689 | C | CA | 29 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0022 others(26): Show |
30 | HG00423.hp1 HG01167.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.168+8779dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073689 | ||||||
chr1:52073689 | CA | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0073 a0001c0001t0001g0114 others(50): Show |
54 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.168+8779delA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073689 | ||||||
chr1:52073689 | CAA | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
119 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.168+8778_168+8779d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073689 | ||||||
chr1:52073689 | CAAA | C | 11 | a0001c0001t0002g0223 a0001c0001t0002g0225 a0001c0001t0006g0016 others(8): Show |
11 | HG00099.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+8777_168+8779d others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073689 | ||||||
chr1:52073689 | CAAAAA | C | 12 | a0001c0001t0002g0089 a0001c0001t0002g0096 a0001c0001t0002g0097 others(9): Show |
12 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+8775_168+8779d others(7): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073689 | ||||||
chr1:52073689 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0008g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.168+8766_168+8779d others(16): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52073689 | ||||||
chr1:52073760 | G | A | 7 | a0001c0001t0003g0002 a0001c0001t0003g0019 a0001c0001t0003g0023 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+8822G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52073760 | |||||||
chr1:52074001 | A | G | 5 | a0001c0001t0003g0063 a0001c0001t0011g0059 a0001c0001t0011g0060 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+9063A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074001 | |||||||
chr1:52074161 | G | GT | 28 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0109 others(25): Show |
30 | HG00099.hp2 HG00140.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.169-9170dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52074161 | ||||||
chr1:52074184 | G | T | 17 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(14): Show |
17 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-9156G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074184 | |||||||
chr1:52074190 | G | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0003g0002 others(19): Show |
24 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.169-9150G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074190 | |||||||
chr1:52074275 | G | A | 1 | a0001c0001t0012g0043 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.169-9065G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074275 | |||||||
chr1:52074316 | A | G | 5 | a0001c0001t0003g0063 a0001c0001t0011g0059 a0001c0001t0011g0060 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-9024A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074316 | |||||||
chr1:52074367 | A | AT | 10 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0193 others(7): Show |
11 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-8959dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52074367 | ||||||
chr1:52074524 | C | T | 8 | a0001c0001t0001g0182 a0001c0001t0008g0074 a0001c0001t0008g0075 others(5): Show |
8 | HG00639.hp2 HG01261.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-8816C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074524 | |||||||
chr1:52074579 | C | G | 1 | a0001c0001t0004g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.169-8761C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074579 | |||||||
chr1:52074701 | T | G | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.169-8639T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074701 | |||||||
chr1:52074924 | T | C | 2 | a0001c0001t0020g0199 a0001c0001t0020g0200 |
2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.169-8416T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52074924 | |||||||
chr1:52075115 | A | C | 1 | a0001c0001t0008g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.169-8225A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075115 | |||||||
chr1:52075130 | G | C | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-8210G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075130 | |||||||
chr1:52075191 | A | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.169-8149A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075191 | |||||||
chr1:52075323 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-8017G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075323 | |||||||
chr1:52075523 | T | TA | 11 | a0001c0001t0001g0127 a0001c0001t0001g0166 a0001c0001t0001g0186 others(8): Show |
11 | HG00642.hp2 HG01175.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-7802dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52075523 | ||||||
chr1:52075523 | TA | T | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-7802delA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52075523 | ||||||
chr1:52075603 | TTATA | T | 10 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(7): Show |
10 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-7733_169-7730d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52075603 | ||||||
chr1:52075607 | A | C | 1 | a0001c0001t0005g0249 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.169-7733A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075607 | |||||||
chr1:52075628 | T | G | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.169-7712T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075628 | |||||||
chr1:52075804 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.169-7536C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075804 | |||||||
chr1:52075831 | T | C | 6 | a0001c0001t0004g0001 a0001c0001t0004g0045 a0001c0001t0004g0057 others(3): Show |
7 | HG00544.hp1 HG00609.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-7509T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075831 | |||||||
chr1:52075853 | C | T | 1 | a0001c0001t0035g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.169-7487C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075853 | |||||||
chr1:52075930 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.169-7410G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075930 | |||||||
chr1:52075947 | G | T | 1 | a0001c0001t0033g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.169-7393G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52075947 | |||||||
chr1:52076080 | G | A | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.169-7260G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52076080 | |||||||
chr1:52076204 | A | T | 6 | a0001c0001t0004g0005 a0001c0001t0004g0046 a0001c0001t0004g0047 others(3): Show |
6 | HG02027.hp2 HG02071.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-7136A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52076204 | |||||||
chr1:52076210 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0171 a0001c0001t0001g0205 |
3 | HG02135.hp2 NA18959.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.169-7130A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52076210 | |||||||
chr1:52076402 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.169-6938C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52076402 | |||||||
chr1:52076458 | T | C | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.169-6882T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52076458 | |||||||
chr1:52076526 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.169-6814G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52076526 | |||||||
chr1:52076593 | C | CA | 10 | a0001c0001t0002g0228 a0001c0001t0007g0015 a0001c0001t0007g0084 others(7): Show |
11 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-6730dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52076593 | ||||||
chr1:52077271 | G | A | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.169-6069G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077271 | |||||||
chr1:52077275 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0011g0059 a0001c0001t0011g0060 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-6065C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077275 | |||||||
chr1:52077544 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.169-5796C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077544 | |||||||
chr1:52077549 | C | T | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-5791C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077549 | |||||||
chr1:52077768 | A | G | 3 | a0001c0001t0013g0168 a0001c0001t0013g0169 a0001c0001t0013g0177 |
3 | HG01243.hp2 HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.169-5572A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077768 | |||||||
chr1:52077772 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.169-5568T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077772 | |||||||
chr1:52077776 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.169-5564A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52077776 | |||||||
chr1:52078157 | A | G | 31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0113 others(28): Show |
33 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.169-5183A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078157 | |||||||
chr1:52078229 | C | CTT | 64 | a0001c0001t0001g0073 a0001c0001t0001g0114 a0001c0001t0001g0142 others(61): Show |
64 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.169-5098_169-5097d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52078229 | ||||||
chr1:52078229 | C | CTTT | 132 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
142 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.169-5099_169-5097d others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52078229 | ||||||
chr1:52078229 | C | CTTTT | 5 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0256 others(2): Show |
5 | HG00099.hp1 HG00639.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-5100_169-5097d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52078229 | ||||||
chr1:52078302 | C | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.169-5038C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078302 | |||||||
chr1:52078402 | T | G | 20 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(17): Show |
21 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.169-4938T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078402 | |||||||
chr1:52078510 | T | C | 1 | a0001c0001t0008g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169-4830T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078510 | |||||||
chr1:52078563 | GC | G | 7 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(4): Show |
8 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-4776delC | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078563 | |||||||
chr1:52078661 | T | C | 4 | a0001c0001t0011g0059 a0001c0001t0011g0060 a0001c0001t0011g0061 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4679T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078661 | |||||||
chr1:52078967 | C | T | 1 | a0001c0001t0013g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169-4373C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52078967 | |||||||
chr1:52079029 | A | G | 11 | a0001c0001t0005g0245 a0001c0001t0005g0247 a0001c0001t0005g0248 others(8): Show |
11 | HG00544.hp2 HG00558.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-4311A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079029 | |||||||
chr1:52079115 | G | C | 1 | a0001c0001t0003g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169-4225G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079115 | |||||||
chr1:52079163 | G | A | 21 | a0001c0001t0001g0208 a0001c0001t0003g0002 a0001c0001t0003g0018 others(18): Show |
22 | HG00140.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-4177G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079163 | |||||||
chr1:52079240 | G | A | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.169-4100G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079240 | |||||||
chr1:52079269 | G | C | 1 | a0001c0001t0008g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.169-4071G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079269 | |||||||
chr1:52079381 | C | CA | 192 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(189): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.169-3943dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52079381 | ||||||
chr1:52079381 | C | CAA | 8 | a0001c0001t0002g0107 a0001c0001t0005g0248 a0001c0001t0007g0015 others(5): Show |
9 | HG02145.hp1 HG02486.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-3944_169-3943d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52079381 | ||||||
chr1:52079430 | G | A | 11 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(8): Show |
11 | HG00099.hp2 HG01175.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-3910G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079430 | |||||||
chr1:52079547 | T | C | 1 | a0001c0001t0013g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169-3793T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079547 | |||||||
chr1:52079695 | G | A | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.169-3645G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079695 | |||||||
chr1:52079695 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0026g0152 |
2 | HG02027.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.169-3645G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079695 | |||||||
chr1:52079757 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169-3583A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079757 | |||||||
chr1:52079761 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169-3579A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079761 | |||||||
chr1:52079857 | TTTTTC | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0242 a0001c0001t0002g0216 |
3 | HG01168.hp1 HG04199.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.169-3468_169-3464d others(7): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52079857 | ||||||
chr1:52079860 | T | C | 1 | a0001c0001t0017g0157 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.169-3480T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079860 | |||||||
chr1:52079868 | TTTTC | T | 179 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.169-3468_169-3465d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52079868 | ||||||
chr1:52079869 | TTTC | T | 19 | a0001c0001t0001g0179 a0001c0001t0005g0247 a0001c0001t0005g0248 others(16): Show |
20 | HG01167.hp2 HG01243.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.169-3468_169-3466d others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52079869 | ||||||
chr1:52079950 | C | A | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.169-3390C>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079950 | |||||||
chr1:52079975 | G | A | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-3365G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52079975 | |||||||
chr1:52080394 | T | C | 4 | a0001c0001t0004g0005 a0001c0001t0004g0047 a0001c0001t0004g0050 others(1): Show |
4 | HG02027.hp2 HG02129.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2946T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080394 | |||||||
chr1:52080446 | A | T | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.169-2894A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080446 | |||||||
chr1:52080460 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169-2880A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080460 | |||||||
chr1:52080519 | G | GT | 11 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0004g0001 others(8): Show |
12 | HG00544.hp1 HG02040.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-2789dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GT | G | 43 | a0001c0001t0001g0173 a0001c0001t0002g0088 a0001c0001t0002g0089 others(40): Show |
45 | HG00544.hp2 HG00673.hp1 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.169-2789delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTT | G | 24 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0155 others(21): Show |
25 | HG00621.hp2 HG00639.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.169-2790_169-2789d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTTT | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0073 a0001c0001t0001g0109 others(47): Show |
51 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.169-2791_169-2789d others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTTTT | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(83): Show |
93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.169-2792_169-2789d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTTTTT | G | 7 | a0001c0001t0001g0165 a0001c0001t0002g0224 a0001c0001t0006g0016 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-2793_169-2789d others(7): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTTTTTT | G | 4 | a0001c0001t0007g0015 a0001c0001t0007g0084 a0001c0001t0007g0239 others(1): Show |
5 | HG02145.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-2794_169-2789d others(8): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTTTTTTT others(4): Show |
G | 5 | a0001c0001t0003g0063 a0001c0001t0011g0059 a0001c0001t0011g0060 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-2799_169-2789d others(13): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080519 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.169-2803_169-2789d others(17): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080519 | ||||||
chr1:52080526 | T | G | 1 | a0001c0001t0008g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.169-2814T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080526 | |||||||
chr1:52080534 | T | G | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.169-2806T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080534 | |||||||
chr1:52080570 | G | C | 1 | a0001c0001t0037g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.169-2770G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080570 | |||||||
chr1:52080582 | A | G | 1 | a0001c0001t0012g0043 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.169-2758A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080582 | |||||||
chr1:52080680 | CCTGCCAC others(5): Show |
C | 1 | a0001c0001t0012g0043 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.169-2656_169-2645d others(14): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080680 | ||||||
chr1:52080786 | G | A | 1 | a0001c0001t0034g0210 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.169-2554G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080786 | |||||||
chr1:52080836 | CT | C | 178 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.169-2482delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080836 | ||||||
chr1:52080836 | CTT | C | 53 | a0001c0001t0001g0101 a0001c0001t0001g0173 a0001c0001t0003g0002 others(50): Show |
57 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.169-2483_169-2482d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52080836 | ||||||
chr1:52080919 | A | C | 14 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-2421A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080919 | |||||||
chr1:52080966 | A | G | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.169-2374A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52080966 | |||||||
chr1:52081085 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.169-2255G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081085 | |||||||
chr1:52081176 | C | T | 1 | a0001c0001t0011g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-2164C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081176 | |||||||
chr1:52081211 | T | TA | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.169-2128dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52081211 | ||||||
chr1:52081224 | GACTCCTG others(58): Show |
G | 1 | a0001c0001t0003g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.169-2114_169-2050d others(67): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52081224 | ||||||
chr1:52081228 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.169-2112C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081228 | |||||||
chr1:52081287 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.169-2053A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081287 | |||||||
chr1:52081561 | T | C | 1 | a0001c0001t0010g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169-1779T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081561 | |||||||
chr1:52081578 | A | G | 251 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(248): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.169-1762A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081578 | |||||||
chr1:52081823 | C | A | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.169-1517C>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081823 | |||||||
chr1:52081950 | C | T | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-1390C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081950 | |||||||
chr1:52081972 | A | C | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-1368A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081972 | |||||||
chr1:52081985 | A | G | 17 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(14): Show |
17 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-1355A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52081985 | |||||||
chr1:52082049 | T | C | 6 | a0001c0001t0001g0137 a0001c0001t0001g0149 a0001c0001t0001g0156 others(3): Show |
6 | HG00738.hp1 HG01106.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-1291T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082049 | |||||||
chr1:52082133 | C | T | 4 | a0001c0001t0003g0065 a0001c0001t0008g0075 a0001c0001t0008g0077 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1207C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082133 | |||||||
chr1:52082276 | A | G | 3 | a0001c0001t0013g0168 a0001c0001t0013g0169 a0001c0001t0013g0177 |
3 | HG01243.hp2 HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.169-1064A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082276 | |||||||
chr1:52082331 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.169-1009A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082331 | |||||||
chr1:52082711 | C | T | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-629C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082711 | |||||||
chr1:52082738 | CA | C | 172 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.169-586delA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52082738 | ||||||
chr1:52082738 | CAA | C | 19 | a0001c0001t0001g0127 a0001c0001t0001g0196 a0001c0001t0002g0118 others(16): Show |
19 | HG00099.hp2 HG01109.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-587_169-586del others(2): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr1 | 52082738 | ||||||
chr1:52082754 | A | T | 2 | a0001c0001t0006g0016 a0001c0001t0006g0218 |
2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.169-586A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082754 | |||||||
chr1:52082965 | C | T | 1 | a0001c0001t0012g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-375C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52082965 | |||||||
chr1:52083049 | T | C | 1 | a0001c0001t0007g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.169-291T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52083049 | |||||||
chr1:52083065 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.169-275C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52083065 | |||||||
chr1:52083092 | T | G | 2 | a0001c0001t0002g0217 a0001c0001t0002g0220 |
2 | HG02896.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.169-248T>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52083092 | |||||||
chr1:52083246 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.169-94G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 3/5 | chr1 | 52083246 | |||||||
chr1:52083589 | G | T | 3 | a0001c0001t0006g0094 a0001c0001t0006g0098 a0001c0001t0031g0244 |
3 | HG00642.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.370+48G>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52083589 | |||||||
chr1:52083820 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0186 a0001c0001t0028g0232 |
4 | HG01168.hp2 HG01169.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+279G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52083820 | |||||||
chr1:52083906 | G | A | 5 | a0001c0001t0005g0245 a0001c0001t0005g0249 a0001c0001t0005g0250 others(2): Show |
5 | HG00544.hp2 HG00558.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.370+365G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52083906 | |||||||
chr1:52083912 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.370+371C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52083912 | |||||||
chr1:52084020 | CA | C | 17 | a0001c0001t0001g0144 a0001c0001t0002g0216 a0001c0001t0002g0217 others(14): Show |
17 | HG00099.hp2 HG01169.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.370+494delA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52084020 | ||||||
chr1:52084203 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.370+662G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084203 | |||||||
chr1:52084294 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370+753C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084294 | |||||||
chr1:52084340 | G | A | 17 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(14): Show |
17 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.370+799G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084340 | |||||||
chr1:52084473 | A | G | 1 | a0001c0001t0008g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.370+932A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084473 | |||||||
chr1:52084608 | A | G | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.370+1067A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084608 | |||||||
chr1:52084775 | AGGG | A | 256 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.370+1238_370+1240d others(5): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52084775 | ||||||
chr1:52084794 | T | TA | 66 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0096 others(63): Show |
70 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.370+1266dupA | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52084794 | ||||||
chr1:52084904 | T | C | 9 | a0001c0001t0002g0097 a0001c0001t0006g0090 a0001c0001t0006g0091 others(6): Show |
9 | HG00642.hp2 HG01884.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.371-1208T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084904 | |||||||
chr1:52084915 | A | C | 1 | a0001c0001t0004g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.371-1197A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52084915 | |||||||
chr1:52085001 | A | T | 1 | a0001c0001t0004g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.371-1111A>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085001 | |||||||
chr1:52085013 | C | CT | 25 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0001t0001g0166 others(22): Show |
25 | HG00099.hp2 HG01175.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.371-1074dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085013 | ||||||
chr1:52085013 | C | CTT | 14 | a0001c0001t0001g0189 a0001c0001t0002g0089 a0001c0001t0002g0096 others(11): Show |
14 | HG00642.hp1 HG01175.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.371-1075_371-1074d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085013 | ||||||
chr1:52085013 | CT | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.371-1074delT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085013 | ||||||
chr1:52085013 | CTT | C | 13 | a0001c0001t0001g0154 a0001c0001t0001g0163 a0001c0001t0001g0187 others(10): Show |
13 | HG00558.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.371-1075_371-1074d others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085013 | ||||||
chr1:52085013 | CTTTT | C | 23 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(20): Show |
26 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.371-1077_371-1074d others(6): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085013 | ||||||
chr1:52085164 | G | A | 7 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0096 others(4): Show |
7 | HG02055.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-948G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085164 | |||||||
chr1:52085165 | C | T | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.371-947C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085165 | |||||||
chr1:52085219 | C | G | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0195 others(2): Show |
5 | HG01257.hp1 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-893C>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085219 | |||||||
chr1:52085230 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.371-882C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085230 | |||||||
chr1:52085288 | G | C | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.371-824G>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085288 | |||||||
chr1:52085303 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0020g0199 a0001c0001t0020g0200 |
3 | HG02258.hp2 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.371-809G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085303 | |||||||
chr1:52085318 | TTTG | T | 252 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(249): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.371-769_371-767del others(3): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085318 | ||||||
chr1:52085318 | TTTGTTGT others(5): Show |
T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0096 |
3 | HG02055.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.371-778_371-767del others(12): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085318 | ||||||
chr1:52085363 | GTTTGTTT others(6): Show |
G | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.371-737_371-725del others(13): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085363 | ||||||
chr1:52085380 | G | GT | 5 | a0001c0001t0002g0223 a0001c0001t0006g0016 a0001c0001t0006g0082 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-722dupT | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085380 | ||||||
chr1:52085411 | C | T | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.371-701C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085411 | |||||||
chr1:52085572 | G | A | 17 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0220 others(14): Show |
17 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.371-540G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085572 | |||||||
chr1:52085577 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.371-535T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085577 | |||||||
chr1:52085591 | G | A | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.371-521G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085591 | |||||||
chr1:52085613 | G | A | 1 | a0001c0001t0024g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.371-499G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085613 | |||||||
chr1:52085666 | A | G | 1 | a0001c0001t0004g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.371-446A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52085666 | |||||||
chr1:52085931 | G | GATTA | 58 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(55): Show |
62 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.371-179_371-176dup others(4): Show |
BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 52085931 | ||||||
chr1:52086053 | A | G | 2 | a0001c0001t0006g0082 a0001c0001t0032g0081 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.371-59A>G | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 4/5 | chr1 | 52086053 | |||||||
chr1:52086322 | C | T | 1 | a0001c0001t0004g0052 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.430+151C>T | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 5/5 | chr1 | 52086322 | |||||||
chr1:52086323 | G | A | 7 | a0001c0001t0008g0074 a0001c0001t0008g0075 a0001c0001t0008g0077 others(4): Show |
7 | HG00639.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+152G>A | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 5/5 | chr1 | 52086323 | |||||||
chr1:52086329 | A | C | 59 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(56): Show |
63 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.430+158A>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 5/5 | chr1 | 52086329 | |||||||
chr1:52086623 | T | C | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.431-89T>C | BTF3L4 | ENSG00000134717.18 | transcript | ENST00000313334.13 | protein_coding | 5/5 | chr1 | 52086623 |