Item | Value |
---|---|
geneid | 51106 |
ensemblid | ENSG00000029639.11 |
hgncid | 17037 |
symbol | TFB1M |
name | transcription factor B1, mitochondrial |
refseq_nuc | NM_016020.4 |
refseq_prot | NP_057104.2 |
ensembl_nuc | ENST00000367166.5 |
ensembl_prot | ENSP00000356134.4 |
mane_status | MANE Select |
chr | chr6 |
start | 155256134 |
end | 155314484 |
strand | - |
ver | v1.2 |
region | chr6:155256134-155314484 |
region5000 | chr6:155251134-155319484 |
regionname0 | TFB1M_chr6_155256134_155314484 |
regionname5000 | TFB1M_chr6_155251134_155319484 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 346 | 345 | 83 | 70 | 144 | 10 | 36 | 120 | TFB1M_chr6_155251134_155319484 | TFB1M | MAASG others(341): Show |
chr6 | 155251134 | 155319484 |
a0002 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | MAASG others(341): Show |
chr6 | 155251134 | 155319484 |
a0003 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | MAASG others(341): Show |
chr6 | 155251134 | 155319484 |
a0004 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | MAASG others(341): Show |
chr6 | 155251134 | 155319484 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1038 | 232 | 50 | 43 | 108 | 5 | 26 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 | ||
a0001c0002 | 1/1 | 1038 | 109 | 31 | 27 | 34 | 5 | 10 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 | ||
a0001c0003 | 0/0 | 1038 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 | ||
a0001c0004 | 0/0 | 1038 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 | ||
a0002c0005 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 | ||
a0003c0007 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 | ||
a0004c0006 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | ATGGC others(1033): Show |
chr6 | 155251134 | 155319484 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2793 | 104 | 13 | 22 | 54 | 2 | 13 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0002 | 0/0 | 2796 | 45 | 1 | 2 | 36 | 0 | 6 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0004 | 0/0 | 2795 | 13 | 2 | 7 | 0 | 2 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0006 | 0/0 | 2795 | 13 | 6 | 5 | 1 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0008 | 0/0 | 2793 | 8 | 0 | 0 | 8 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0009 | 0/0 | 2794 | 7 | 2 | 1 | 2 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2789): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0012 | 0/0 | 2796 | 6 | 6 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0013 | 0/0 | 2793 | 5 | 3 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0014 | 0/0 | 2796 | 4 | 3 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0015 | 0/0 | 2796 | 3 | 0 | 0 | 3 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0016 | 0/0 | 2797 | 3 | 1 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2792): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0017 | 0/0 | 2793 | 3 | 2 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0018 | 0/0 | 2795 | 3 | 2 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0021 | 0/0 | 2795 | 2 | 0 | 0 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0024 | 0/0 | 2793 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0025 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0026 | 0/0 | 2794 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2789): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0028 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0030 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0031 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0033 | 0/0 | 2794 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2789): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0034 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0040 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0001t0042 | 0/0 | 2794 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2789): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0003 | 0/0 | 2795 | 30 | 1 | 12 | 13 | 2 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0004 | 0/0 | 2795 | 13 | 12 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0005 | 1/1 | 2799 | 26 | 8 | 12 | 1 | 3 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2794): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0006 | 0/0 | 2795 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0007 | 0/0 | 2795 | 9 | 0 | 0 | 9 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0010 | 0/0 | 2799 | 7 | 2 | 0 | 2 | 0 | 3 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2794): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0011 | 0/0 | 2796 | 6 | 0 | 0 | 6 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0014 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0019 | 0/0 | 2800 | 3 | 0 | 3 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2795): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0022 | 0/0 | 2800 | 2 | 0 | 0 | 1 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2795): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0023 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0027 | 0/0 | 2798 | 2 | 0 | 0 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2793): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0029 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0035 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0036 | 0/0 | 2795 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0037 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0001c0002t0041 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2795): Show |
chr6 | 155251134 | 155319484 |
a0001c0003t0001 | 0/0 | 2793 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2788): Show |
chr6 | 155251134 | 155319484 |
a0001c0004t0020 | 0/0 | 2794 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2789): Show |
chr6 | 155251134 | 155319484 |
a0002c0005t0039 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2790): Show |
chr6 | 155251134 | 155319484 |
a0003c0007t0032 | 0/0 | 2794 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2789): Show |
chr6 | 155251134 | 155319484 |
a0004c0006t0038 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | GGAGC others(2791): Show |
chr6 | 155251134 | 155319484 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0015g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0015g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0016g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0016g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0017g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0017g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0018g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0018g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0021g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0021g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0024g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0024g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0025g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0025g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0026g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0028g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0030g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0031g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0033g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0034g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0040g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0042g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0010 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0014g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0019g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0019g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0022g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0022g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0027g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0027g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0029g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0035g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0036g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0037g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0041g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0004t0020g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0004t0020g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0002c0005t0039g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0003c0007t0032g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0004c0006t0038g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0224 | EUR | GBR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0006 | EUR | GBR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00280 | hp1 | a0001 | c0002 | t0005 | g0262 | EUR | FIN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0189 | EUR | FIN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0036 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0252 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00738 | hp2 | a0001 | c0001 | t0040 | g0292 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00741 | hp1 | a0001 | c0002 | t0019 | g0264 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00741 | hp2 | a0001 | c0001 | t0017 | g0248 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01069 | hp2 | a0001 | c0002 | t0005 | g0255 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01070 | hp1 | a0001 | c0001 | t0018 | g0249 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0183 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0182 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01074 | hp2 | a0001 | c0002 | t0005 | g0238 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0253 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0177 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0221 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01109 | hp1 | a0001 | c0001 | t0013 | g0029 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01167 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0202 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0201 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0156 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01255 | hp2 | a0001 | c0001 | t0014 | g0222 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01256 | hp1 | a0001 | c0002 | t0019 | g0024 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0254 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0009 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01358 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01361 | hp1 | a0001 | c0002 | t0005 | g0244 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01496 | hp1 | a0001 | c0002 | t0019 | g0024 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0245 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0213 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01515 | hp2 | a0001 | c0002 | t0005 | g0010 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0009 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0212 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01884 | hp1 | a0001 | c0002 | t0005 | g0261 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0259 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01891 | hp1 | a0002 | c0005 | t0039 | g0305 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01934 | hp1 | a0001 | c0002 | t0005 | g0240 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01975 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02040 | hp1 | a0001 | c0001 | t0015 | g0205 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0258 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02056 | hp1 | a0001 | c0001 | t0009 | g0129 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02071 | hp1 | a0001 | c0002 | t0007 | g0206 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02129 | hp1 | a0001 | c0002 | t0007 | g0161 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02145 | hp1 | a0001 | c0004 | t0020 | g0163 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0215 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02155 | hp2 | a0001 | c0001 | t0015 | g0084 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0233 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02258 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0209 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0204 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02451 | hp2 | a0001 | c0002 | t0004 | g0043 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02523 | hp2 | a0001 | c0002 | t0007 | g0160 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02572 | hp1 | a0001 | c0001 | t0016 | g0265 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02602 | hp2 | a0001 | c0002 | t0027 | g0242 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02622 | hp1 | a0003 | c0007 | t0032 | g0052 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02622 | hp2 | a0001 | c0001 | t0028 | g0028 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02647 | hp1 | a0001 | c0002 | t0010 | g0048 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0044 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0164 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0049 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02809 | hp2 | a0001 | c0001 | t0026 | g0023 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0260 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0257 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02895 | hp1 | a0001 | c0001 | t0024 | g0230 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02896 | hp1 | a0001 | c0001 | t0017 | g0251 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02897 | hp1 | a0001 | c0001 | t0024 | g0229 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02922 | hp1 | a0001 | c0002 | t0014 | g0053 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0237 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0130 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0217 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02970 | hp2 | a0001 | c0002 | t0023 | g0047 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0192 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0042 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0227 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0046 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03139 | hp2 | a0001 | c0001 | t0025 | g0304 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03195 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03209 | hp2 | a0001 | c0002 | t0037 | g0050 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03225 | hp2 | a0001 | c0002 | t0004 | g0039 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0203 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03239 | hp2 | a0001 | c0002 | t0027 | g0241 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03453 | hp1 | a0001 | c0002 | t0010 | g0034 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03453 | hp2 | a0001 | c0001 | t0026 | g0023 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03486 | hp2 | a0001 | c0001 | t0042 | g0306 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03490 | hp2 | a0001 | c0002 | t0010 | g0055 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03491 | hp2 | a0001 | c0002 | t0010 | g0181 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03540 | hp1 | a0001 | c0002 | t0029 | g0027 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03540 | hp2 | a0001 | c0001 | t0025 | g0303 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03579 | hp2 | a0001 | c0001 | t0030 | g0051 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03688 | hp1 | a0001 | c0002 | t0041 | g0243 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03688 | hp2 | a0001 | c0002 | t0022 | g0179 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03831 | hp1 | a0001 | c0002 | t0010 | g0180 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0108 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03927 | hp1 | a0001 | c0001 | t0009 | g0071 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03927 | hp2 | a0001 | c0002 | t0035 | g0178 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04115 | hp1 | a0001 | c0001 | t0034 | g0150 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04184 | hp1 | a0001 | c0001 | t0021 | g0035 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04204 | hp1 | a0001 | c0001 | t0021 | g0037 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0041 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18522 | hp2 | a0001 | c0002 | t0005 | g0246 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18943 | hp1 | a0001 | c0002 | t0007 | g0207 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18948 | hp2 | a0001 | c0002 | t0011 | g0187 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18951 | hp2 | a0001 | c0002 | t0011 | g0188 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18954 | hp1 | a0001 | c0002 | t0007 | g0159 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18956 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18965 | hp2 | a0001 | c0002 | t0010 | g0058 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18970 | hp1 | a0001 | c0001 | t0016 | g0272 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0093 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18972 | hp2 | a0001 | c0002 | t0011 | g0200 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18973 | hp2 | a0001 | c0001 | t0008 | g0081 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18981 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18982 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18995 | hp1 | a0001 | c0001 | t0033 | g0122 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19001 | hp2 | a0001 | c0002 | t0011 | g0195 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19002 | hp1 | a0001 | c0002 | t0007 | g0020 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19004 | hp1 | a0001 | c0001 | t0031 | g0136 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19005 | hp1 | a0001 | c0002 | t0010 | g0056 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19006 | hp1 | a0001 | c0002 | t0036 | g0185 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19007 | hp1 | a0001 | c0002 | t0007 | g0208 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19010 | hp1 | a0001 | c0002 | t0007 | g0020 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19012 | hp2 | a0001 | c0001 | t0016 | g0302 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19043 | hp1 | a0001 | c0002 | t0023 | g0038 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19043 | hp2 | a0001 | c0004 | t0020 | g0162 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19056 | hp1 | a0001 | c0002 | t0005 | g0239 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19056 | hp2 | a0001 | c0002 | t0011 | g0190 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19064 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19065 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19066 | hp1 | a0001 | c0002 | t0011 | g0184 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19067 | hp1 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19067 | hp2 | a0001 | c0002 | t0022 | g0057 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19081 | hp2 | a0001 | c0002 | t0007 | g0059 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19090 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19240 | hp2 | a0004 | c0006 | t0038 | g0231 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0247 | AFR | ASW | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0225 | AFR | ASW | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0176 | SAS | GIH | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0220 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0234 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02109 | hp1 | a0001 | c0002 | t0005 | g0236 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0175 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0250 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02486 | hp2 | a0001 | c0002 | t0006 | g0216 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02559 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03471 | hp1 | a0001 | c0002 | t0006 | g0054 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0256 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | USA | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
homoSapiens | chm13v2 | a0001 | c0002 | t0005 | g0010 | REF | REF | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
homoSapiens | grch38p0 | a0001 | c0002 | t0005 | g0235 | REF | REF | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155260300 | C | T | 1 | a0004 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.767G>A | p.Arg256Gln | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/7 | 823/2799 | 767/1041 | 256/346 | chr6 | 155260300 | |||
chr6:155297084 | T | C | 1 | a0003 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.415A>G | p.Ile139Val | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/7 | 471/2799 | 415/1041 | 139/346 | chr6 | 155297084 | |||
chr6:155298554 | C | T | 1 | a0002 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.317G>A | p.Arg106Lys | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/7 | 373/2799 | 317/1041 | 106/346 | chr6 | 155298554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155257986 | G | A | 1 | a0001c0003 | 2 | NA18969.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.891C>T | p.Ile297Ile | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 947/2799 | 891/1041 | 297/346 | chr6 | 155257986 | |||
chr6:155285191 | C | T | 5 | a0001c0001 a0001c0003 a0001c0004 others(2): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
synonymous_variant | LOW | c.633G>A | p.Thr211Thr | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/7 | 689/2799 | 633/1041 | 211/346 | chr6 | 155285191 | |||
chr6:155311293 | G | A | 1 | a0001c0004 | 2 | HG02145.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.180C>T | p.Tyr60Tyr | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/7 | 236/2799 | 180/1041 | 60/346 | chr6 | 155311293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155256240 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(34): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1596A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1596 | chr6 | 155256240 | ||||||
chr6:155256247 | A | G | 1 | a0001c0004t0020 | 2 | HG02145.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1589T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1589 | chr6 | 155256247 | ||||||
chr6:155256580 | G | C | 2 | a0001c0001t0013 a0001c0001t0021 |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1256C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1256 | chr6 | 155256580 | ||||||
chr6:155256582 | T | C | 2 | a0001c0001t0013 a0001c0001t0021 |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1254A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1254 | chr6 | 155256582 | ||||||
chr6:155256583 | T | A | 2 | a0001c0001t0013 a0001c0001t0021 |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1253A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1253 | chr6 | 155256583 | ||||||
chr6:155256689 | C | T | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(32): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1147G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1147 | chr6 | 155256689 | ||||||
chr6:155256731 | T | A | 2 | a0001c0001t0008 a0001c0001t0033 |
9 | NA18941.hp2 NA18949.hp2 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1105 | chr6 | 155256731 | ||||||
chr6:155256738 | C | T | 1 | a0001c0001t0021 | 2 | HG04184.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1098G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1098 | chr6 | 155256738 | ||||||
chr6:155256831 | G | A | 1 | a0001c0002t0041 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1005 | chr6 | 155256831 | ||||||
chr6:155256833 | G | A | 1 | a0001c0001t0025 | 2 | HG03139.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1003C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1003 | chr6 | 155256833 | ||||||
chr6:155256876 | G | A | 2 | a0001c0002t0007 a0001c0002t0035 |
10 | HG02071.hp1 HG02129.hp1 HG02523.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 960 | chr6 | 155256876 | ||||||
chr6:155256942 | A | G | 1 | a0002c0005t0039 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*894T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 894 | chr6 | 155256942 | ||||||
chr6:155257155 | A | C | 2 | a0001c0004t0020 a0003c0007t0032 |
3 | HG02145.hp1 HG02622.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*681T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 681 | chr6 | 155257155 | ||||||
chr6:155257190 | C | CA | 11 | a0001c0001t0012 a0001c0001t0014 a0001c0002t0011 others(8): Show |
28 | HG00741.hp1 HG01255.hp2 HG01256.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*645dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 645 | chr6 | 155257190 | ||||||
chr6:155257190 | CA | C | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0015 others(8): Show |
67 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*645delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 645 | chr6 | 155257190 | ||||||
chr6:155257190 | CAA | C | 11 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0013 others(8): Show |
129 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*644_*645delTT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 644 | chr6 | 155257190 | ||||||
chr6:155257206 | A | C | 1 | a0001c0001t0031 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 630 | chr6 | 155257206 | ||||||
chr6:155257214 | G | A | 1 | a0001c0001t0034 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 622 | chr6 | 155257214 | ||||||
chr6:155257384 | A | ATT | 7 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(4): Show |
56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451dupAA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 451 | chr6 | 155257384 | ||||||
chr6:155257432 | T | C | 1 | a0001c0002t0036 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 404 | chr6 | 155257432 | ||||||
chr6:155257465 | A | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(33): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*371T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 371 | chr6 | 155257465 | ||||||
chr6:155257550 | G | A | 5 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0011 others(2): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 286 | chr6 | 155257550 | ||||||
chr6:155257579 | AAGAT | A | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(37): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*253_*256delATCT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 253 | chr6 | 155257579 | ||||||
chr6:155257622 | A | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(33): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*214T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 214 | chr6 | 155257622 | ||||||
chr6:155314448 | C | A | 2 | a0001c0001t0024 a0004c0006t0038 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-20G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 20 | chr6 | 155314448 | ||||||
chr6:155314451 | A | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(29): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 23 | chr6 | 155314451 | ||||||
chr6:155314452 | C | A | 1 | a0001c0001t0042 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 24 | chr6 | 155314452 | ||||||
chr6:155314461 | A | C | 2 | a0001c0001t0028 a0001c0002t0029 |
2 | HG02622.hp2 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-33T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 33 | chr6 | 155314461 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155258112 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.795-30T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258112 | |||||||
chr6:155258158 | A | G | 1 | a0001c0002t0027g0241 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.795-76T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258158 | |||||||
chr6:155258244 | A | G | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.795-162T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258244 | |||||||
chr6:155258249 | C | T | 2 | a0001c0002t0005g0239 a0001c0002t0005g0240 |
2 | HG01934.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.795-167G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258249 | |||||||
chr6:155258266 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(161): Show |
188 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.795-184T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258266 | |||||||
chr6:155258283 | C | T | 1 | a0001c0002t0019g0024 | 2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.795-201G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258283 | |||||||
chr6:155258284 | G | A | 1 | a0001c0001t0009g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.795-202C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258284 | |||||||
chr6:155258408 | T | C | 3 | a0001c0001t0013g0036 a0001c0001t0021g0035 a0001c0001t0021g0037 |
3 | HG00639.hp1 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.795-326A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258408 | |||||||
chr6:155258423 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(246): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.795-341T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258423 | |||||||
chr6:155258510 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.795-428G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258510 | |||||||
chr6:155258547 | A | AAT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(246): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.795-467_795-466dup others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258547 | |||||||
chr6:155258614 | G | A | 9 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 others(6): Show |
9 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-532C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258614 | |||||||
chr6:155258694 | C | T | 2 | a0001c0001t0008g0083 a0001c0001t0014g0225 |
2 | NA18977.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.795-612G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258694 | |||||||
chr6:155258805 | T | C | 1 | a0001c0001t0002g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.795-723A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258805 | |||||||
chr6:155258881 | G | A | 1 | a0001c0002t0004g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.795-799C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258881 | |||||||
chr6:155258900 | CTGA | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.795-821_795-819del others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258900 | |||||||
chr6:155258962 | C | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0135 |
2 | HG01099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.795-880G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258962 | |||||||
chr6:155259134 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.795-1052A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259134 | |||||||
chr6:155259140 | C | T | 2 | a0001c0001t0004g0164 a0001c0001t0004g0176 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.795-1058G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259140 | |||||||
chr6:155259207 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.794+1066T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259207 | |||||||
chr6:155259213 | C | T | 5 | a0001c0002t0003g0022 a0001c0002t0003g0193 a0001c0002t0003g0196 others(2): Show |
6 | NA18939.hp2 NA18983.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+1060G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259213 | |||||||
chr6:155259240 | C | T | 1 | a0001c0002t0003g0022 | 2 | NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.794+1033G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259240 | |||||||
chr6:155259442 | T | C | 1 | a0001c0002t0005g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.794+831A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259442 | |||||||
chr6:155259504 | G | A | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+769C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259504 | |||||||
chr6:155259620 | A | AT | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.794+652dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259620 | |||||||
chr6:155259639 | T | G | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.794+634A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259639 | |||||||
chr6:155259749 | T | G | 5 | a0001c0002t0003g0186 a0001c0002t0003g0192 a0001c0002t0011g0184 others(2): Show |
5 | HG03017.hp1 NA18948.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+524A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259749 | |||||||
chr6:155259890 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(163): Show |
190 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.794+383C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259890 | |||||||
chr6:155260018 | G | C | 1 | a0001c0001t0002g0299 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.794+255C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260018 | |||||||
chr6:155260052 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.794+221G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260052 | |||||||
chr6:155260083 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.794+190C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260083 | |||||||
chr6:155260155 | C | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.794+118G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260155 | |||||||
chr6:155260237 | A | G | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.794+36T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260237 | |||||||
chr6:155260254 | G | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.794+19C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260254 | |||||||
chr6:155260485 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-85C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260485 | |||||||
chr6:155260589 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.667-189C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260589 | |||||||
chr6:155260601 | G | A | 11 | a0001c0001t0004g0164 a0001c0001t0004g0166 a0001c0001t0004g0167 others(8): Show |
11 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-201C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260601 | |||||||
chr6:155260701 | T | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-301A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260701 | |||||||
chr6:155260763 | A | G | 47 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(44): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.667-363T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260763 | |||||||
chr6:155260770 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-370G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260770 | |||||||
chr6:155261081 | T | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-681A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261081 | |||||||
chr6:155261122 | A | C | 1 | a0001c0001t0009g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-722T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261122 | |||||||
chr6:155261216 | G | A | 50 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(47): Show |
56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.667-816C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261216 | |||||||
chr6:155261331 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-931G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261331 | |||||||
chr6:155261342 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0098 others(3): Show |
8 | HG00642.hp1 HG01081.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-942G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261342 | |||||||
chr6:155261393 | T | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-993A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261393 | |||||||
chr6:155261611 | T | G | 25 | a0001c0001t0006g0007 a0001c0001t0006g0174 a0001c0001t0006g0218 others(22): Show |
28 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.667-1211A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261611 | |||||||
chr6:155261617 | AGGTGCCT others(2): Show |
A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-1226_667-1218d others(11): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261617 | |||||||
chr6:155261670 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.667-1270A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261670 | |||||||
chr6:155261704 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-1304G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261704 | |||||||
chr6:155261708 | G | A | 5 | a0001c0002t0005g0008 a0001c0002t0005g0237 a0001c0002t0005g0245 others(2): Show |
7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-1308C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261708 | |||||||
chr6:155261814 | C | G | 53 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(50): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.667-1414G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261814 | |||||||
chr6:155262132 | G | C | 1 | a0001c0002t0005g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.667-1732C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262132 | |||||||
chr6:155262155 | G | A | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-1755C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262155 | |||||||
chr6:155262156 | T | C | 1 | a0001c0001t0004g0172 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.667-1756A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262156 | |||||||
chr6:155262163 | G | A | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-1763C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262163 | |||||||
chr6:155262252 | G | A | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-1852C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262252 | |||||||
chr6:155262405 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0090 others(1): Show |
4 | HG01257.hp2 HG02683.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-2005G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262405 | |||||||
chr6:155262411 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(216): Show |
249 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(246): Show |
intron_variant | MODIFIER | c.667-2011C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262411 | |||||||
chr6:155262452 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.667-2052G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262452 | |||||||
chr6:155262457 | G | T | 1 | a0001c0001t0014g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.667-2057C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262457 | |||||||
chr6:155262470 | C | G | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-2070G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262470 | |||||||
chr6:155262486 | G | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(217): Show |
250 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(247): Show |
intron_variant | MODIFIER | c.667-2086C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262486 | |||||||
chr6:155262524 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.667-2124C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262524 | |||||||
chr6:155262539 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-2139T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262539 | |||||||
chr6:155262733 | G | GA | 23 | a0001c0001t0006g0007 a0001c0001t0006g0174 a0001c0001t0006g0218 others(20): Show |
26 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.667-2334dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262733 | |||||||
chr6:155262862 | A | T | 1 | a0001c0002t0035g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.667-2462T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262862 | |||||||
chr6:155262949 | T | C | 1 | a0001c0001t0006g0220 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.667-2549A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262949 | |||||||
chr6:155263030 | A | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-2630T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263030 | |||||||
chr6:155263222 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(245): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.667-2822A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263222 | |||||||
chr6:155263535 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.667-3135G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263535 | |||||||
chr6:155263576 | G | A | 1 | a0001c0001t0013g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.667-3176C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263576 | |||||||
chr6:155263610 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.667-3210G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263610 | |||||||
chr6:155263619 | G | C | 1 | a0001c0001t0018g0249 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.667-3219C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263619 | |||||||
chr6:155263742 | CAT | C | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-3344_667-3343d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263742 | |||||||
chr6:155263746 | T | C | 1 | a0001c0001t0009g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-3346A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263746 | |||||||
chr6:155263944 | T | TG | 22 | a0001c0001t0006g0007 a0001c0001t0006g0174 a0001c0001t0006g0218 others(19): Show |
25 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.667-3545dupC | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263944 | |||||||
chr6:155263946 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(246): Show |
281 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(278): Show |
intron_variant | MODIFIER | c.667-3546T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263946 | |||||||
chr6:155264020 | G | A | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-3620C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264020 | |||||||
chr6:155264099 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(283): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.667-3699T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264099 | |||||||
chr6:155264144 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(216): Show |
249 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(246): Show |
intron_variant | MODIFIER | c.667-3744G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264144 | |||||||
chr6:155264164 | G | A | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-3764C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264164 | |||||||
chr6:155264177 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.667-3777C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264177 | |||||||
chr6:155264191 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(120): Show |
139 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(136): Show |
intron_variant | MODIFIER | c.667-3791G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264191 | |||||||
chr6:155264531 | C | T | 5 | a0001c0002t0005g0008 a0001c0002t0005g0237 a0001c0002t0005g0245 others(2): Show |
7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-4131G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264531 | |||||||
chr6:155264600 | TC | T | 5 | a0001c0002t0005g0008 a0001c0002t0005g0237 a0001c0002t0005g0245 others(2): Show |
7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-4201delG | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264600 | |||||||
chr6:155264734 | G | A | 50 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(47): Show |
56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.667-4334C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264734 | |||||||
chr6:155264784 | G | T | 1 | a0001c0002t0004g0005 | 3 | HG02818.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.667-4384C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264784 | |||||||
chr6:155264817 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.667-4417T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264817 | |||||||
chr6:155264930 | C | T | 5 | a0001c0002t0005g0008 a0001c0002t0005g0237 a0001c0002t0005g0245 others(2): Show |
7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-4530G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264930 | |||||||
chr6:155264997 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.667-4597G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264997 | |||||||
chr6:155264998 | A | G | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-4598T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264998 | |||||||
chr6:155265355 | T | C | 2 | a0001c0002t0007g0020 a0001c0002t0007g0059 |
3 | NA19002.hp1 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.667-4955A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265355 | |||||||
chr6:155265442 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.667-5042C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265442 | |||||||
chr6:155265462 | G | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(49): Show |
58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.667-5062C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265462 | |||||||
chr6:155265464 | A | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-5064T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265464 | |||||||
chr6:155265487 | T | C | 6 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-5087A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265487 | |||||||
chr6:155265503 | CAGA | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-5106_667-5104d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265503 | |||||||
chr6:155265671 | G | A | 2 | a0001c0002t0006g0054 a0001c0002t0014g0053 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.667-5271C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265671 | |||||||
chr6:155265706 | T | A | 1 | a0001c0002t0019g0264 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.667-5306A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265706 | |||||||
chr6:155265729 | A | AATATATA others(22): Show |
1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.667-5358_667-5330d others(31): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265729 | |||||||
chr6:155265730 | ATATATAT | A | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-5337_667-5331d others(9): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265730 | |||||||
chr6:155265735 | T | C | 1 | a0003c0007t0032g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.667-5335A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265735 | |||||||
chr6:155265736 | A | T | 1 | a0001c0001t0009g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-5336T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265736 | |||||||
chr6:155265738 | T | A | 8 | a0001c0001t0001g0040 a0001c0001t0002g0263 a0001c0001t0004g0171 others(5): Show |
8 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-5338A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265738 | |||||||
chr6:155266001 | C | T | 9 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(6): Show |
10 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-5601G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266001 | |||||||
chr6:155266063 | C | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(214): Show |
247 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(244): Show |
intron_variant | MODIFIER | c.667-5663G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266063 | |||||||
chr6:155266111 | C | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-5711G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266111 | |||||||
chr6:155266288 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-5888T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266288 | |||||||
chr6:155266333 | C | G | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.667-5933G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266333 | |||||||
chr6:155266462 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6062T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266462 | |||||||
chr6:155266568 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-6168A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266568 | |||||||
chr6:155266575 | T | A | 1 | a0001c0002t0011g0188 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.667-6175A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266575 | |||||||
chr6:155266575 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(238): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.667-6175A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266575 | |||||||
chr6:155266613 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6213T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266613 | |||||||
chr6:155266642 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.667-6242G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266642 | |||||||
chr6:155266708 | G | A | 1 | a0001c0001t0009g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-6308C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266708 | |||||||
chr6:155266771 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6371A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266771 | |||||||
chr6:155266778 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG00673.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.667-6378G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266778 | |||||||
chr6:155266841 | C | T | 52 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(49): Show |
58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.667-6441G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266841 | |||||||
chr6:155266846 | C | CA | 18 | a0001c0001t0004g0164 a0001c0001t0004g0167 a0001c0001t0004g0169 others(15): Show |
18 | HG01109.hp2 HG01243.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.667-6447dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | |||||||
chr6:155266846 | CAA | C | 16 | a0001c0001t0001g0094 a0001c0001t0009g0228 a0001c0001t0012g0025 others(13): Show |
17 | HG00741.hp2 HG01175.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.667-6448_667-6447d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | |||||||
chr6:155266846 | CAAA | C | 73 | a0001c0001t0001g0040 a0001c0001t0001g0073 a0001c0001t0001g0087 others(70): Show |
81 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.667-6449_667-6447d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | |||||||
chr6:155266846 | CAAAA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(148): Show |
175 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.667-6450_667-6447d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | |||||||
chr6:155266970 | C | CT | 26 | a0001c0001t0001g0040 a0001c0001t0004g0164 a0001c0001t0004g0166 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.667-6571dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266970 | |||||||
chr6:155266970 | C | CTTT | 8 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0259 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-6573_667-6571d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266970 | |||||||
chr6:155266970 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
128 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.667-6571delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266970 | |||||||
chr6:155267024 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-6624G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267024 | |||||||
chr6:155267037 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.667-6637A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267037 | |||||||
chr6:155267134 | C | T | 50 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(47): Show |
56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.667-6734G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267134 | |||||||
chr6:155267223 | C | T | 4 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-6823G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267223 | |||||||
chr6:155267241 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6841A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267241 | |||||||
chr6:155267254 | C | T | 4 | a0001c0001t0002g0263 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-6854G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267254 | |||||||
chr6:155267255 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6855T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267255 | |||||||
chr6:155267321 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-6921G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267321 | |||||||
chr6:155267327 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6927C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267327 | |||||||
chr6:155267350 | T | C | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-6950A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267350 | |||||||
chr6:155267424 | G | C | 1 | a0001c0001t0002g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.667-7024C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267424 | |||||||
chr6:155267548 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.667-7148A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267548 | |||||||
chr6:155267752 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.667-7352C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267752 | |||||||
chr6:155267781 | T | A | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-7381A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267781 | |||||||
chr6:155267793 | C | G | 1 | a0001c0002t0007g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.667-7393G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267793 | |||||||
chr6:155268639 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-8239C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268639 | |||||||
chr6:155268698 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.667-8298C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268698 | |||||||
chr6:155268736 | G | A | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-8336C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268736 | |||||||
chr6:155268757 | T | C | 121 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(118): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.667-8357A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268757 | |||||||
chr6:155268757 | T | G | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-8357A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268757 | |||||||
chr6:155268759 | C | T | 128 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(125): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.667-8359G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268759 | |||||||
chr6:155268800 | CACAA | C | 4 | a0001c0001t0002g0277 a0001c0001t0002g0282 a0001c0001t0002g0285 others(1): Show |
4 | NA18941.hp1 NA18975.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-8404_667-8401d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268800 | |||||||
chr6:155268811 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-8411G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268811 | |||||||
chr6:155268820 | G | C | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-8420C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268820 | |||||||
chr6:155268897 | A | G | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-8497T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268897 | |||||||
chr6:155268954 | A | G | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-8554T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268954 | |||||||
chr6:155268986 | TA | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(236): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.667-8587delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268986 | |||||||
chr6:155268986 | TAA | T | 12 | a0001c0001t0001g0040 a0001c0001t0001g0105 a0001c0001t0002g0286 others(9): Show |
12 | HG00639.hp1 HG01109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.667-8588_667-8587d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268986 | |||||||
chr6:155269065 | C | T | 1 | a0001c0002t0006g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.667-8665G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269065 | |||||||
chr6:155269098 | T | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-8698A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269098 | |||||||
chr6:155269140 | T | C | 1 | a0003c0007t0032g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.667-8740A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269140 | |||||||
chr6:155269154 | G | C | 2 | a0001c0002t0003g0182 a0001c0002t0003g0183 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.667-8754C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269154 | |||||||
chr6:155269304 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.667-8904C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269304 | |||||||
chr6:155269304 | GTTTTC | G | 5 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-8909_667-8905d others(7): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269304 | |||||||
chr6:155269324 | C | CTT | 8 | a0001c0001t0001g0151 a0001c0001t0013g0029 a0001c0001t0013g0030 others(5): Show |
8 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-8926_667-8925d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269324 | |||||||
chr6:155269324 | C | CTTT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
154 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.667-8927_667-8925d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269324 | |||||||
chr6:155269324 | C | CTTTT | 94 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0002g0004 others(91): Show |
108 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.667-8928_667-8925d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269324 | |||||||
chr6:155269329 | T | C | 1 | a0001c0002t0037g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.667-8929A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269329 | |||||||
chr6:155269384 | C | T | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-8984G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269384 | |||||||
chr6:155269408 | G | A | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.667-9008C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269408 | |||||||
chr6:155269447 | G | A | 1 | a0001c0001t0006g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.667-9047C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269447 | |||||||
chr6:155269455 | G | A | 9 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(6): Show |
10 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-9055C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269455 | |||||||
chr6:155269559 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-9159G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269559 | |||||||
chr6:155269564 | C | T | 1 | a0001c0002t0003g0196 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.667-9164G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269564 | |||||||
chr6:155269675 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(179): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.667-9275T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269675 | |||||||
chr6:155269950 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(177): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.667-9550G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269950 | |||||||
chr6:155269952 | A | G | 1 | a0001c0001t0040g0292 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.667-9552T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269952 | |||||||
chr6:155269990 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.667-9590A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269990 | |||||||
chr6:155270265 | C | G | 2 | a0001c0002t0003g0182 a0001c0002t0003g0183 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.667-9865G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270265 | |||||||
chr6:155270270 | G | A | 39 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(36): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.667-9870C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270270 | |||||||
chr6:155270283 | C | G | 1 | a0001c0001t0034g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.667-9883G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270283 | |||||||
chr6:155270417 | A | G | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-10017T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270417 | |||||||
chr6:155270501 | C | T | 17 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 others(14): Show |
18 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.667-10101G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270501 | |||||||
chr6:155270565 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.667-10165A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270565 | |||||||
chr6:155270705 | C | G | 10 | a0001c0001t0006g0174 a0001c0001t0012g0025 a0001c0001t0012g0256 others(7): Show |
11 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-10305G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270705 | |||||||
chr6:155270950 | T | G | 63 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(60): Show |
69 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.667-10550A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270950 | |||||||
chr6:155270956 | C | T | 1 | a0001c0001t0014g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.667-10556G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270956 | |||||||
chr6:155271052 | G | A | 1 | a0001c0002t0005g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.667-10652C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271052 | |||||||
chr6:155271171 | G | C | 7 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(4): Show |
8 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-10771C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271171 | |||||||
chr6:155271376 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.667-10976A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271376 | |||||||
chr6:155271523 | G | C | 1 | a0001c0002t0003g0210 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.667-11123C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271523 | |||||||
chr6:155271574 | T | G | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-11174A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271574 | |||||||
chr6:155271867 | G | A | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-11467C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271867 | |||||||
chr6:155271927 | G | T | 1 | a0001c0002t0011g0200 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.667-11527C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271927 | |||||||
chr6:155272265 | G | A | 58 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(55): Show |
64 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.667-11865C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272265 | |||||||
chr6:155272574 | G | C | 2 | a0001c0001t0006g0174 a0001c0001t0014g0175 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-12174C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272574 | |||||||
chr6:155272691 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.667-12291G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272691 | |||||||
chr6:155272797 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.666+12361G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272797 | |||||||
chr6:155272895 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+12263T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272895 | |||||||
chr6:155273124 | A | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+12034T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273124 | |||||||
chr6:155273257 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0009g0228 a0003c0007t0032g0052 |
3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.666+11901T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273257 | |||||||
chr6:155273503 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(243): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.666+11655G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273503 | |||||||
chr6:155273641 | A | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(243): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.666+11517T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273641 | |||||||
chr6:155273648 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.666+11510G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273648 | |||||||
chr6:155273792 | C | T | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+11366G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273792 | |||||||
chr6:155273810 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+11348A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273810 | |||||||
chr6:155273985 | T | G | 3 | a0001c0002t0003g0182 a0001c0002t0003g0183 a0001c0002t0003g0204 |
3 | HG01070.hp2 HG01071.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.666+11173A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273985 | |||||||
chr6:155274062 | C | T | 2 | a0001c0002t0006g0215 a0001c0002t0006g0216 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.666+11096G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274062 | |||||||
chr6:155274074 | A | G | 2 | a0001c0001t0013g0032 a0001c0001t0013g0033 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.666+11084T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274074 | |||||||
chr6:155274097 | G | T | 1 | a0001c0001t0002g0269 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.666+11061C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274097 | |||||||
chr6:155274158 | C | T | 2 | a0001c0002t0005g0238 a0001c0002t0041g0243 |
2 | HG01074.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.666+11000G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274158 | |||||||
chr6:155274348 | G | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+10810C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274348 | |||||||
chr6:155274418 | A | G | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+10740T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274418 | |||||||
chr6:155274559 | G | A | 1 | a0001c0002t0007g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.666+10599C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274559 | |||||||
chr6:155274564 | G | T | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+10594C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274564 | |||||||
chr6:155274688 | G | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+10470C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274688 | |||||||
chr6:155274691 | T | C | 2 | a0001c0001t0026g0023 a0001c0001t0042g0306 |
3 | HG02809.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.666+10467A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274691 | |||||||
chr6:155274748 | C | T | 1 | a0001c0001t0040g0292 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.666+10410G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274748 | |||||||
chr6:155274939 | C | T | 6 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0223 others(3): Show |
6 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+10219G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274939 | |||||||
chr6:155274993 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(238): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.666+10165G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274993 | |||||||
chr6:155275062 | CA | C | 56 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(53): Show |
62 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.666+10095delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275062 | |||||||
chr6:155275083 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+10075C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275083 | |||||||
chr6:155275098 | C | T | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+10060G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275098 | |||||||
chr6:155275151 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+10007T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275151 | |||||||
chr6:155275212 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+9946A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275212 | |||||||
chr6:155275335 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.666+9823C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275335 | |||||||
chr6:155275346 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.666+9812G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275346 | |||||||
chr6:155275349 | T | C | 2 | a0001c0001t0025g0303 a0001c0001t0025g0304 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.666+9809A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275349 | |||||||
chr6:155275385 | A | C | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+9773T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275385 | |||||||
chr6:155275482 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+9676G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275482 | |||||||
chr6:155275566 | T | C | 60 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(57): Show |
66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.666+9592A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275566 | |||||||
chr6:155275721 | T | A | 1 | a0001c0001t0015g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.666+9437A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275721 | |||||||
chr6:155275730 | C | G | 2 | a0001c0001t0025g0303 a0001c0001t0025g0304 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.666+9428G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275730 | |||||||
chr6:155275767 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+9391A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275767 | |||||||
chr6:155275871 | G | A | 1 | a0001c0001t0002g0278 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.666+9287C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275871 | |||||||
chr6:155275980 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.666+9178C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275980 | |||||||
chr6:155275999 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+9159C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275999 | |||||||
chr6:155276013 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+9145G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276013 | |||||||
chr6:155276071 | T | A | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+9087A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276071 | |||||||
chr6:155276265 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.666+8893G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276265 | |||||||
chr6:155276340 | C | T | 1 | a0003c0007t0032g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.666+8818G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276340 | |||||||
chr6:155276510 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+8648T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276510 | |||||||
chr6:155276534 | T | G | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+8624A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276534 | |||||||
chr6:155276552 | C | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+8606G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276552 | |||||||
chr6:155276620 | G | A | 4 | a0001c0001t0008g0081 a0001c0001t0008g0083 a0001c0001t0008g0124 others(1): Show |
4 | NA18941.hp2 NA18973.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+8538C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276620 | |||||||
chr6:155276664 | C | CTTTTTT | 242 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(239): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+8493_666+8494i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276664 | |||||||
chr6:155277008 | T | C | 47 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(44): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.666+8150A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277008 | |||||||
chr6:155277041 | C | T | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+8117G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277041 | |||||||
chr6:155277091 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.666+8067A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277091 | |||||||
chr6:155277167 | A | G | 1 | a0001c0002t0037g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666+7991T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277167 | |||||||
chr6:155277543 | A | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.666+7615T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277543 | |||||||
chr6:155277761 | C | A | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+7397G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277761 | |||||||
chr6:155277855 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+7303G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277855 | |||||||
chr6:155278074 | C | T | 1 | a0001c0002t0003g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666+7084G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278074 | |||||||
chr6:155278251 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+6907G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278251 | |||||||
chr6:155278284 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01243.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.666+6874G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278284 | |||||||
chr6:155278403 | C | T | 16 | a0001c0001t0004g0164 a0001c0001t0004g0166 a0001c0001t0004g0167 others(13): Show |
16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.666+6755G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278403 | |||||||
chr6:155278589 | C | T | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+6569G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278589 | |||||||
chr6:155278692 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.666+6466A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278692 | |||||||
chr6:155278751 | G | A | 12 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(9): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.666+6407C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278751 | |||||||
chr6:155278770 | G | A | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+6388C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278770 | |||||||
chr6:155278831 | C | T | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | NA18944.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.666+6327G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278831 | |||||||
chr6:155279073 | T | C | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+6085A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279073 | |||||||
chr6:155279125 | A | T | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+6033T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279125 | |||||||
chr6:155279213 | C | CT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+5944dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279213 | |||||||
chr6:155279213 | C | CTT | 8 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0123 others(5): Show |
8 | NA18939.hp1 NA18944.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.666+5943_666+5944d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279213 | |||||||
chr6:155279245 | A | T | 4 | a0001c0001t0002g0296 a0001c0001t0002g0298 a0001c0001t0002g0301 others(1): Show |
4 | NA18949.hp1 NA18952.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+5913T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279245 | |||||||
chr6:155279631 | T | C | 1 | a0001c0001t0004g0170 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.666+5527A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279631 | |||||||
chr6:155279683 | T | A | 1 | a0001c0002t0004g0005 | 3 | HG02818.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.666+5475A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279683 | |||||||
chr6:155279684 | T | A | 14 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(11): Show |
16 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.666+5474A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279684 | |||||||
chr6:155279708 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.666+5450A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279708 | |||||||
chr6:155279777 | C | T | 5 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0223 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+5381G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279777 | |||||||
chr6:155279779 | C | A | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+5379G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279779 | |||||||
chr6:155279991 | A | C | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+5167T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279991 | |||||||
chr6:155280045 | T | A | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+5113A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280045 | |||||||
chr6:155280056 | G | T | 1 | a0001c0002t0005g0246 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.666+5102C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280056 | |||||||
chr6:155280060 | A | C | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666+5098T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280060 | |||||||
chr6:155280350 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(211): Show |
239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+4808T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280350 | |||||||
chr6:155280351 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(211): Show |
239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+4807G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280351 | |||||||
chr6:155280384 | C | T | 16 | a0001c0001t0004g0164 a0001c0001t0004g0166 a0001c0001t0004g0167 others(13): Show |
16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.666+4774G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280384 | |||||||
chr6:155280399 | T | C | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666+4759A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280399 | |||||||
chr6:155280427 | G | A | 1 | a0001c0002t0019g0024 | 2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.666+4731C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280427 | |||||||
chr6:155280455 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+4703G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280455 | |||||||
chr6:155280677 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.666+4481T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280677 | |||||||
chr6:155280741 | A | T | 1 | a0001c0002t0007g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.666+4417T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280741 | |||||||
chr6:155280794 | C | G | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+4364G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280794 | |||||||
chr6:155280868 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(151): Show |
173 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(170): Show |
intron_variant | MODIFIER | c.666+4290G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280868 | |||||||
chr6:155280932 | A | G | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+4226T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280932 | |||||||
chr6:155281431 | T | G | 2 | a0001c0001t0025g0303 a0001c0001t0025g0304 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.666+3727A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281431 | |||||||
chr6:155281448 | G | T | 60 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(57): Show |
66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.666+3710C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281448 | |||||||
chr6:155281492 | C | T | 1 | a0001c0002t0004g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.666+3666G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281492 | |||||||
chr6:155281520 | G | A | 1 | a0001c0002t0011g0195 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.666+3638C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281520 | |||||||
chr6:155281538 | A | T | 1 | a0001c0001t0002g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.666+3620T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281538 | |||||||
chr6:155281599 | G | C | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | NA18944.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.666+3559C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281599 | |||||||
chr6:155281615 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(214): Show |
242 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(239): Show |
intron_variant | MODIFIER | c.666+3543C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281615 | |||||||
chr6:155281655 | G | C | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+3503C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281655 | |||||||
chr6:155281721 | C | CA | 16 | a0001c0001t0001g0118 a0001c0001t0002g0283 a0001c0001t0002g0284 others(13): Show |
17 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+3436dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | |||||||
chr6:155281721 | C | CAA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(124): Show |
148 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.666+3435_666+3436d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | |||||||
chr6:155281721 | C | CAAA | 43 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0062 others(40): Show |
45 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.666+3434_666+3436d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | |||||||
chr6:155281721 | CA | C | 38 | a0001c0001t0004g0166 a0001c0001t0004g0168 a0001c0001t0004g0169 others(35): Show |
41 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.666+3436delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | |||||||
chr6:155281821 | T | TA | 91 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(88): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.666+3336dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281821 | |||||||
chr6:155281821 | TA | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(112): Show |
131 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.666+3336delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281821 | |||||||
chr6:155281838 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.666+3320A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281838 | |||||||
chr6:155281915 | G | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+3243C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281915 | |||||||
chr6:155282063 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(209): Show |
237 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(234): Show |
intron_variant | MODIFIER | c.666+3095A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282063 | |||||||
chr6:155282063 | T | G | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+3095A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282063 | |||||||
chr6:155282385 | A | G | 2 | a0001c0002t0006g0215 a0001c0002t0006g0216 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.666+2773T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282385 | |||||||
chr6:155282395 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+2763G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282395 | |||||||
chr6:155282537 | A | G | 39 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(36): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.666+2621T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282537 | |||||||
chr6:155282802 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.666+2356C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282802 | |||||||
chr6:155282886 | C | A | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+2272G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282886 | |||||||
chr6:155282917 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+2241G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282917 | |||||||
chr6:155283012 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.666+2146A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283012 | |||||||
chr6:155283133 | C | T | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+2025G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283133 | |||||||
chr6:155283180 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+1978G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283180 | |||||||
chr6:155283246 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+1912A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283246 | |||||||
chr6:155283422 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+1736G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283422 | |||||||
chr6:155283661 | T | C | 2 | a0001c0001t0004g0164 a0001c0001t0004g0176 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.666+1497A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283661 | |||||||
chr6:155283671 | C | A | 1 | a0001c0002t0005g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.666+1487G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283671 | |||||||
chr6:155283673 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG02129.hp2 HG02135.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.666+1485C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283673 | |||||||
chr6:155283710 | T | C | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+1448A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283710 | |||||||
chr6:155283778 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.666+1380A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283778 | |||||||
chr6:155283866 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+1292A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283866 | |||||||
chr6:155283958 | T | C | 1 | a0001c0002t0003g0197 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.666+1200A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283958 | |||||||
chr6:155283968 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(211): Show |
239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+1190C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283968 | |||||||
chr6:155284074 | G | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+1084C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284074 | |||||||
chr6:155284092 | G | A | 9 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(6): Show |
9 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+1066C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284092 | |||||||
chr6:155284353 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(150): Show |
172 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(169): Show |
intron_variant | MODIFIER | c.666+805T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284353 | |||||||
chr6:155284353 | A | T | 1 | a0001c0001t0014g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666+805T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284353 | |||||||
chr6:155284421 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.666+737A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284421 | |||||||
chr6:155284441 | G | C | 1 | a0001c0001t0025g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666+717C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284441 | |||||||
chr6:155284793 | G | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+365C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284793 | |||||||
chr6:155285043 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+115C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155285043 | |||||||
chr6:155285326 | T | A | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.547-49A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285326 | |||||||
chr6:155285397 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(211): Show |
239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.547-120T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285397 | |||||||
chr6:155285407 | C | T | 1 | a0001c0001t0002g0297 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.547-130G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285407 | |||||||
chr6:155285413 | CAT | C | 6 | a0001c0002t0003g0021 a0001c0002t0003g0191 a0001c0002t0003g0210 others(3): Show |
7 | HG00673.hp1 NA18972.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-138_547-137del others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285413 | |||||||
chr6:155285433 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-156C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285433 | |||||||
chr6:155285576 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0226 |
4 | HG02280.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-299C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285576 | |||||||
chr6:155285831 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-554C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285831 | |||||||
chr6:155285888 | T | G | 6 | a0001c0001t0002g0026 a0001c0001t0002g0271 a0001c0001t0002g0286 others(3): Show |
7 | NA18948.hp1 NA18960.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-611A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285888 | |||||||
chr6:155285901 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.547-624T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285901 | |||||||
chr6:155285959 | T | C | 1 | a0001c0001t0002g0275 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.547-682A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285959 | |||||||
chr6:155286167 | G | T | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-890C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286167 | |||||||
chr6:155286339 | C | T | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-1062G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286339 | |||||||
chr6:155286355 | AAGAC | A | 42 | a0001c0001t0001g0067 a0001c0002t0003g0003 a0001c0002t0003g0006 others(39): Show |
50 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.547-1082_547-1079d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286355 | |||||||
chr6:155286419 | A | G | 2 | a0001c0001t0002g0232 a0001c0001t0002g0268 |
2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.547-1142T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286419 | |||||||
chr6:155286479 | A | G | 12 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(9): Show |
14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.547-1202T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286479 | |||||||
chr6:155286481 | GTGTGTGT others(7): Show |
G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(248): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.547-1218_547-1205d others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286481 | |||||||
chr6:155286481 | GTGTGTGT others(21): Show |
G | 2 | a0001c0001t0006g0218 a0001c0001t0006g0219 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.547-1232_547-1205d others(30): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286481 | |||||||
chr6:155286489 | ATATATAT others(45): Show |
A | 9 | a0001c0002t0004g0005 a0001c0002t0004g0041 a0001c0002t0004g0042 others(6): Show |
11 | HG02451.hp2 HG02717.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-1264_547-1213d others(54): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286489 | |||||||
chr6:155286497 | GTGTGTAT others(33): Show |
G | 4 | a0001c0002t0003g0186 a0001c0002t0011g0184 a0001c0002t0011g0187 others(1): Show |
4 | NA18948.hp2 NA18951.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1260_547-1221d others(42): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286497 | |||||||
chr6:155286503 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0092 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.547-1227_547-1226i others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286503 | |||||||
chr6:155286551 | GTGTATAT others(3): Show |
G | 1 | a0001c0001t0004g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.547-1284_547-1275d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286551 | |||||||
chr6:155286585 | GTATATGT others(5): Show |
G | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547-1320_547-1309d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286585 | |||||||
chr6:155286603 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(134): Show |
154 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.547-1326C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286603 | |||||||
chr6:155286603 | GTGTGTAT others(5): Show |
G | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-1338_547-1327d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286603 | |||||||
chr6:155286615 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(195): Show |
221 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(218): Show |
intron_variant | MODIFIER | c.547-1338T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286615 | |||||||
chr6:155286620 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(137): Show |
157 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.547-1343A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286620 | |||||||
chr6:155286626 | T | C | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-1349A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286626 | |||||||
chr6:155286637 | A | G | 1 | a0004c0006t0038g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.547-1360T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286637 | |||||||
chr6:155286637 | ATG | A | 44 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(41): Show |
50 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.547-1362_547-1361d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286637 | |||||||
chr6:155286649 | GTA | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
128 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.547-1374_547-1373d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286649 | |||||||
chr6:155286659 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1382T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286659 | |||||||
chr6:155286661 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1384C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286661 | |||||||
chr6:155286668 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1391A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286668 | |||||||
chr6:155286670 | C | CAT | 6 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-1395_547-1394d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286670 | |||||||
chr6:155286670 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1393G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286670 | |||||||
chr6:155286681 | A | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0137 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.547-1404T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286681 | |||||||
chr6:155286683 | T | A | 3 | a0001c0002t0003g0022 a0001c0002t0003g0196 a0001c0002t0003g0198 |
4 | NA18983.hp1 NA19004.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1406A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286683 | |||||||
chr6:155286779 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-1502A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286779 | |||||||
chr6:155286802 | C | T | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-1525G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286802 | |||||||
chr6:155286819 | A | G | 42 | a0001c0001t0001g0067 a0001c0002t0003g0003 a0001c0002t0003g0006 others(39): Show |
50 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.547-1542T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286819 | |||||||
chr6:155286985 | G | A | 47 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(44): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.547-1708C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286985 | |||||||
chr6:155286986 | A | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-1709T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286986 | |||||||
chr6:155287157 | G | A | 16 | a0001c0001t0004g0164 a0001c0001t0004g0166 a0001c0001t0004g0167 others(13): Show |
16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.547-1880C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287157 | |||||||
chr6:155287225 | T | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0125 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.547-1948A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287225 | |||||||
chr6:155287321 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(137): Show |
157 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.547-2044G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287321 | |||||||
chr6:155287398 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.547-2121A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287398 | |||||||
chr6:155287532 | ACTC | A | 52 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(49): Show |
58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.547-2258_547-2256d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287532 | |||||||
chr6:155287535 | C | G | 1 | a0001c0001t0002g0274 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.547-2258G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287535 | |||||||
chr6:155287551 | A | AGTGT | 41 | a0001c0001t0001g0100 a0001c0001t0001g0123 a0001c0001t0001g0127 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.547-2278_547-2275d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGT | 35 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(32): Show |
39 | HG00609.hp2 HG00673.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.547-2280_547-2275d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(1): Show |
69 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(66): Show |
81 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.547-2282_547-2275d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0095 others(9): Show |
12 | HG00621.hp2 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.547-2284_547-2275d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(5): Show |
33 | a0001c0001t0001g0092 a0001c0001t0001g0133 a0001c0001t0004g0164 others(30): Show |
36 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.547-2286_547-2275d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(7): Show |
19 | a0001c0001t0001g0040 a0001c0001t0002g0274 a0001c0001t0002g0278 others(16): Show |
19 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.547-2288_547-2275d others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(9): Show |
42 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(39): Show |
48 | HG00558.hp2 HG00621.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.547-2290_547-2275d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(11): Show |
3 | a0001c0001t0002g0267 a0001c0001t0006g0226 a0001c0001t0009g0228 |
3 | HG00609.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.547-2292_547-2275d others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(13): Show |
1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-2294_547-2275d others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(15): Show |
1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-2296_547-2275d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287551 | A | AGTGTGTG others(17): Show |
1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-2298_547-2275d others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | |||||||
chr6:155287856 | T | C | 1 | a0001c0002t0004g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.547-2579A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287856 | |||||||
chr6:155287896 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(119): Show |
139 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.547-2619G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287896 | |||||||
chr6:155287900 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.547-2623A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287900 | |||||||
chr6:155287959 | T | G | 1 | a0001c0001t0002g0277 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.547-2682A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287959 | |||||||
chr6:155288269 | G | T | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-2992C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288269 | |||||||
chr6:155288382 | T | C | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-3105A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288382 | |||||||
chr6:155288568 | T | A | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-3291A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288568 | |||||||
chr6:155288588 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0086 others(8): Show |
12 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.547-3311T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288588 | |||||||
chr6:155288616 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-3339C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288616 | |||||||
chr6:155288948 | G | C | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-3671C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288948 | |||||||
chr6:155289064 | G | GT | 107 | a0001c0001t0001g0067 a0001c0001t0001g0123 a0001c0001t0002g0004 others(104): Show |
123 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.547-3788dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289064 | |||||||
chr6:155289115 | T | G | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-3838A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289115 | |||||||
chr6:155289125 | C | T | 1 | a0001c0002t0003g0209 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.547-3848G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289125 | |||||||
chr6:155289166 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.547-3889A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289166 | |||||||
chr6:155289252 | GAA | G | 28 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0070 others(25): Show |
33 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.547-3977_547-3976d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289252 | |||||||
chr6:155289258 | G | C | 1 | a0001c0001t0012g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.547-3981C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289258 | |||||||
chr6:155289290 | A | C | 3 | a0001c0001t0006g0223 a0001c0001t0006g0224 a0001c0001t0018g0233 |
3 | HG00099.hp1 HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.547-4013T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289290 | |||||||
chr6:155289368 | C | G | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-4091G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289368 | |||||||
chr6:155289685 | T | C | 2 | a0001c0002t0005g0250 a0001c0002t0005g0255 |
2 | HG01069.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.547-4408A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289685 | |||||||
chr6:155289742 | G | A | 6 | a0001c0001t0008g0002 a0001c0001t0008g0081 a0001c0001t0008g0083 others(3): Show |
9 | NA18941.hp2 NA18949.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.547-4465C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289742 | |||||||
chr6:155289756 | G | T | 1 | a0001c0002t0023g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.547-4479C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289756 | |||||||
chr6:155289766 | C | T | 1 | a0003c0007t0032g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.547-4489G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289766 | |||||||
chr6:155289833 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.547-4556A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289833 | |||||||
chr6:155289888 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-4611C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289888 | |||||||
chr6:155289995 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.547-4718A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289995 | |||||||
chr6:155290023 | G | C | 1 | a0001c0001t0033g0122 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.547-4746C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290023 | |||||||
chr6:155290057 | A | C | 1 | a0001c0001t0014g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.547-4780T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290057 | |||||||
chr6:155290252 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.547-4975C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290252 | |||||||
chr6:155290335 | G | A | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-5058C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290335 | |||||||
chr6:155290373 | G | A | 2 | a0001c0001t0001g0070 a0001c0002t0003g0197 |
2 | HG02683.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.547-5096C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290373 | |||||||
chr6:155290388 | C | CAAAA | 36 | a0001c0001t0001g0067 a0001c0002t0003g0003 a0001c0002t0003g0006 others(33): Show |
44 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.547-5115_547-5112d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290388 | |||||||
chr6:155290406 | A | AAAG | 6 | a0001c0001t0001g0094 a0001c0001t0001g0113 a0001c0001t0001g0165 others(3): Show |
6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-5130_547-5129i others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | |||||||
chr6:155290406 | A | AAG | 183 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
208 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(205): Show |
intron_variant | MODIFIER | c.547-5130_547-5129i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | |||||||
chr6:155290406 | A | AG | 16 | a0001c0001t0001g0040 a0001c0001t0001g0097 a0001c0001t0001g0135 others(13): Show |
16 | HG00621.hp1 HG01099.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.547-5130_547-5129i others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | |||||||
chr6:155290406 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.547-5129T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | |||||||
chr6:155290602 | T | C | 1 | a0001c0002t0003g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.547-5325A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290602 | |||||||
chr6:155290769 | G | C | 1 | a0001c0002t0010g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.547-5492C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290769 | |||||||
chr6:155290913 | C | G | 2 | a0001c0002t0006g0054 a0001c0002t0014g0053 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.547-5636G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290913 | |||||||
chr6:155291029 | CCTGAGTT others(3): Show |
C | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-5762_547-5753d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291029 | |||||||
chr6:155291079 | A | G | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-5802T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291079 | |||||||
chr6:155291083 | A | G | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-5806T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291083 | |||||||
chr6:155291161 | G | A | 1 | a0001c0002t0003g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.546+5792C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291161 | |||||||
chr6:155291225 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+5728T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291225 | |||||||
chr6:155291758 | T | C | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546+5195A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291758 | |||||||
chr6:155291765 | A | T | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+5188T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291765 | |||||||
chr6:155291844 | G | C | 1 | a0001c0002t0005g0246 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.546+5109C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291844 | |||||||
chr6:155291878 | A | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(28): Show |
35 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.546+5075T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291878 | |||||||
chr6:155291957 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+4996C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291957 | |||||||
chr6:155292013 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+4940T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292013 | |||||||
chr6:155292297 | A | T | 1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.546+4656T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292297 | |||||||
chr6:155292345 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.546+4608A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292345 | |||||||
chr6:155292429 | C | T | 2 | a0001c0001t0026g0023 a0001c0001t0042g0306 |
3 | HG02809.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.546+4524G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292429 | |||||||
chr6:155292539 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+4414C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292539 | |||||||
chr6:155292580 | A | G | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.546+4373T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292580 | |||||||
chr6:155292597 | T | C | 1 | a0001c0001t0012g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546+4356A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292597 | |||||||
chr6:155292598 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+4355A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292598 | |||||||
chr6:155292634 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+4319T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292634 | |||||||
chr6:155292772 | A | G | 39 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(36): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.546+4181T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292772 | |||||||
chr6:155292885 | A | T | 1 | a0001c0001t0002g0278 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546+4068T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292885 | |||||||
chr6:155292983 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(242): Show |
276 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(273): Show |
intron_variant | MODIFIER | c.546+3970G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292983 | |||||||
chr6:155293012 | TG | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG00621.hp2 HG02135.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.546+3940delC | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293012 | |||||||
chr6:155293058 | C | T | 39 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(36): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.546+3895G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293058 | |||||||
chr6:155293157 | T | TCATA | 104 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(101): Show |
118 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.546+3792_546+3795d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | |||||||
chr6:155293157 | T | TCATACAT others(1): Show |
40 | a0001c0001t0004g0164 a0001c0001t0004g0166 a0001c0001t0004g0167 others(37): Show |
43 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.546+3788_546+3795d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | |||||||
chr6:155293157 | T | TCATACAT others(5): Show |
111 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
127 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.546+3784_546+3795d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | |||||||
chr6:155293157 | T | TCATACAT others(9): Show |
3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0008g0083 |
3 | NA18973.hp1 NA18977.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.546+3780_546+3795d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | |||||||
chr6:155293238 | A | G | 2 | a0001c0002t0003g0182 a0001c0002t0003g0183 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.546+3715T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293238 | |||||||
chr6:155293249 | G | A | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.546+3704C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293249 | |||||||
chr6:155293619 | T | C | 1 | a0004c0006t0038g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.546+3334A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293619 | |||||||
chr6:155293747 | C | T | 60 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(57): Show |
66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.546+3206G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293747 | |||||||
chr6:155293748 | T | G | 1 | a0001c0001t0018g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.546+3205A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293748 | |||||||
chr6:155293938 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.546+3015T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293938 | |||||||
chr6:155293991 | C | T | 1 | a0001c0001t0013g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.546+2962G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293991 | |||||||
chr6:155294105 | G | A | 44 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(41): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.546+2848C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294105 | |||||||
chr6:155294114 | C | T | 3 | a0001c0001t0006g0007 a0001c0001t0006g0226 a0001c0001t0006g0227 |
5 | HG02280.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+2839G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294114 | |||||||
chr6:155294176 | T | C | 2 | a0001c0001t0004g0164 a0001c0001t0004g0176 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.546+2777A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294176 | |||||||
chr6:155294214 | T | C | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+2739A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294214 | |||||||
chr6:155294238 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(111): Show |
130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.546+2715T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294238 | |||||||
chr6:155294480 | A | G | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+2473T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294480 | |||||||
chr6:155294594 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+2359T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294594 | |||||||
chr6:155294657 | G | A | 39 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(36): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.546+2296C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294657 | |||||||
chr6:155294706 | G | A | 1 | a0001c0002t0003g0199 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.546+2247C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294706 | |||||||
chr6:155294728 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.546+2225A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294728 | |||||||
chr6:155294814 | C | T | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.546+2139G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294814 | |||||||
chr6:155294851 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+2102T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294851 | |||||||
chr6:155295095 | A | G | 1 | a0001c0001t0014g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.546+1858T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295095 | |||||||
chr6:155295137 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.546+1816G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295137 | |||||||
chr6:155295142 | G | C | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546+1811C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295142 | |||||||
chr6:155295222 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+1731G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295222 | |||||||
chr6:155295283 | G | A | 44 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(41): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.546+1670C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295283 | |||||||
chr6:155295479 | T | C | 1 | a0001c0002t0004g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.546+1474A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295479 | |||||||
chr6:155295580 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
156 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(153): Show |
intron_variant | MODIFIER | c.546+1373G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295580 | |||||||
chr6:155295653 | C | T | 2 | a0001c0002t0005g0010 a0001c0002t0005g0262 |
3 | HG00280.hp1 HG01515.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.546+1300G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295653 | |||||||
chr6:155295680 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.546+1273A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295680 | |||||||
chr6:155295763 | T | C | 47 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(44): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.546+1190A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295763 | |||||||
chr6:155295815 | C | A | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.546+1138G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295815 | |||||||
chr6:155295970 | C | T | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+983G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295970 | |||||||
chr6:155296059 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(255): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+894C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296059 | |||||||
chr6:155296096 | T | C | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+857A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296096 | |||||||
chr6:155296107 | G | T | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+846C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296107 | |||||||
chr6:155296147 | G | A | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+806C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296147 | |||||||
chr6:155296246 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.546+707A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296246 | |||||||
chr6:155296265 | C | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.546+688G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296265 | |||||||
chr6:155296407 | C | A | 41 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.546+546G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296407 | |||||||
chr6:155296426 | A | AT | 67 | a0001c0001t0001g0040 a0001c0001t0001g0086 a0001c0001t0001g0087 others(64): Show |
73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.546+526dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | |||||||
chr6:155296426 | A | ATT | 9 | a0001c0001t0002g0275 a0001c0001t0002g0282 a0001c0001t0002g0290 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+525_546+526dup others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | |||||||
chr6:155296426 | AT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
109 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.546+526delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | |||||||
chr6:155296426 | ATTTTTTT | A | 38 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(35): Show |
45 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.546+520_546+526del others(7): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | |||||||
chr6:155296426 | ATTTTTTT others(1): Show |
A | 8 | a0001c0002t0003g0022 a0001c0002t0003g0193 a0001c0002t0003g0194 others(5): Show |
9 | NA18939.hp2 NA18981.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+519_546+526del others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | |||||||
chr6:155296530 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.546+423C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296530 | |||||||
chr6:155296687 | A | AGTGGCAT others(19): Show |
58 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(55): Show |
64 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.546+240_546+265dup others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296687 | |||||||
chr6:155296688 | G | GTGGCATC others(19): Show |
1 | a0001c0001t0002g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546+264_546+265ins others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296688 | |||||||
chr6:155297212 | T | C | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-108A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297212 | |||||||
chr6:155297232 | A | C | 1 | a0001c0001t0004g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395-128T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297232 | |||||||
chr6:155297318 | G | A | 1 | a0003c0007t0032g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.395-214C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297318 | |||||||
chr6:155297536 | T | C | 1 | a0001c0001t0015g0084 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.395-432A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297536 | |||||||
chr6:155297703 | G | T | 2 | a0001c0001t0013g0029 a0001c0001t0013g0030 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.395-599C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297703 | |||||||
chr6:155297883 | G | A | 1 | a0001c0001t0008g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.394+594C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297883 | |||||||
chr6:155297889 | A | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(253): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.394+588T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297889 | |||||||
chr6:155298107 | A | G | 14 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(11): Show |
16 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.394+370T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155298107 | |||||||
chr6:155298299 | G | A | 52 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(49): Show |
58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.394+178C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155298299 | |||||||
chr6:155298727 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.286-142G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155298727 | |||||||
chr6:155298841 | T | A | 52 | a0001c0001t0001g0040 a0001c0001t0002g0004 a0001c0001t0002g0011 others(49): Show |
58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.286-256A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155298841 | |||||||
chr6:155299092 | G | C | 44 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0021 others(41): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.286-507C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299092 | |||||||
chr6:155299104 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0144 |
2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.286-519G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299104 | |||||||
chr6:155299659 | T | C | 1 | a0001c0001t0004g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.286-1074A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299659 | |||||||
chr6:155299762 | T | C | 47 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(44): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.286-1177A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299762 | |||||||
chr6:155299885 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
156 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(153): Show |
intron_variant | MODIFIER | c.286-1300C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299885 | |||||||
chr6:155299918 | T | C | 45 | a0001c0001t0001g0067 a0001c0002t0003g0003 a0001c0002t0003g0006 others(42): Show |
53 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.286-1333A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299918 | |||||||
chr6:155300057 | C | A | 1 | a0001c0001t0014g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286-1472G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300057 | |||||||
chr6:155300106 | T | C | 1 | a0003c0007t0032g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286-1521A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300106 | |||||||
chr6:155300277 | T | G | 1 | a0001c0001t0009g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.286-1692A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300277 | |||||||
chr6:155300295 | T | C | 2 | a0001c0002t0006g0215 a0001c0002t0006g0216 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.286-1710A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300295 | |||||||
chr6:155300378 | T | G | 1 | a0001c0002t0011g0200 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.286-1793A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300378 | |||||||
chr6:155300423 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0085 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-1838T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300423 | |||||||
chr6:155300478 | CCA | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.286-1895_286-1894d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300478 | |||||||
chr6:155300493 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0009g0228 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.286-1908G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300493 | |||||||
chr6:155300524 | T | C | 1 | a0001c0001t0014g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286-1939A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300524 | |||||||
chr6:155300551 | T | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG03490.hp1 HG03492.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.286-1966A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300551 | |||||||
chr6:155300688 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(135): Show |
155 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.286-2103C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300688 | |||||||
chr6:155300804 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286-2219A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300804 | |||||||
chr6:155300867 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
6 | HG00738.hp2 HG01433.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2282G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300867 | |||||||
chr6:155300931 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.286-2346T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300931 | |||||||
chr6:155300936 | C | G | 7 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-2351G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300936 | |||||||
chr6:155300954 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(253): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.286-2369T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300954 | |||||||
chr6:155301124 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0009g0120 |
2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.286-2539A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301124 | |||||||
chr6:155301347 | T | C | 114 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0002g0004 others(111): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.286-2762A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301347 | |||||||
chr6:155301507 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286-2922T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301507 | |||||||
chr6:155301514 | C | A | 3 | a0001c0001t0001g0137 a0001c0001t0009g0228 a0001c0002t0037g0050 |
3 | HG02970.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.286-2929G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301514 | |||||||
chr6:155301764 | C | T | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-3179G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301764 | |||||||
chr6:155301828 | A | G | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-3243T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301828 | |||||||
chr6:155302145 | T | A | 1 | a0001c0001t0008g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.286-3560A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302145 | |||||||
chr6:155302146 | C | G | 1 | a0001c0001t0008g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.286-3561G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302146 | |||||||
chr6:155302156 | A | G | 1 | a0001c0001t0008g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.286-3571T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302156 | |||||||
chr6:155302178 | C | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(271): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.286-3593G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302178 | |||||||
chr6:155302196 | T | C | 2 | a0001c0001t0028g0028 a0001c0002t0029g0027 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.286-3611A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302196 | |||||||
chr6:155302490 | G | A | 44 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(41): Show |
50 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.286-3905C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302490 | |||||||
chr6:155302575 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(250): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.286-3990C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302575 | |||||||
chr6:155302715 | T | C | 1 | a0001c0001t0009g0129 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.286-4130A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302715 | |||||||
chr6:155302768 | T | C | 1 | a0001c0001t0025g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.286-4183A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302768 | |||||||
chr6:155302829 | A | C | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-4244T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302829 | |||||||
chr6:155302836 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286-4251T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302836 | |||||||
chr6:155302907 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286-4322T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302907 | |||||||
chr6:155302945 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(272): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.286-4360T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302945 | |||||||
chr6:155302948 | C | T | 4 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0010g0058 others(1): Show |
4 | HG03490.hp2 NA18965.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-4363G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302948 | |||||||
chr6:155303022 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.286-4437T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303022 | |||||||
chr6:155303140 | CTAATTT | C | 17 | a0001c0001t0001g0165 a0001c0001t0004g0164 a0001c0001t0004g0166 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.286-4561_286-4556d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303140 | |||||||
chr6:155303169 | C | A | 3 | a0001c0001t0006g0174 a0001c0001t0014g0175 a0001c0001t0014g0217 |
3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.286-4584G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303169 | |||||||
chr6:155303184 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286-4599T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303184 | |||||||
chr6:155303191 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.286-4606T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303191 | |||||||
chr6:155303218 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(179): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.286-4633C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303218 | |||||||
chr6:155303231 | C | T | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-4646G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303231 | |||||||
chr6:155303400 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286-4815A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303400 | |||||||
chr6:155303464 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(249): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.286-4879G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303464 | |||||||
chr6:155303558 | G | A | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-4973C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303558 | |||||||
chr6:155303582 | T | C | 2 | a0001c0002t0004g0046 a0001c0002t0023g0047 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.286-4997A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303582 | |||||||
chr6:155303593 | G | A | 4 | a0001c0002t0004g0005 a0001c0002t0004g0046 a0001c0002t0023g0047 others(1): Show |
6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-5008C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303593 | |||||||
chr6:155303642 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286-5057A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303642 | |||||||
chr6:155303869 | A | G | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286-5284T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303869 | |||||||
chr6:155303970 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.286-5385T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303970 | |||||||
chr6:155303990 | A | G | 4 | a0001c0002t0004g0005 a0001c0002t0004g0046 a0001c0002t0023g0047 others(1): Show |
6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-5405T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303990 | |||||||
chr6:155304078 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.286-5493G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304078 | |||||||
chr6:155304155 | G | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(49): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.286-5570C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304155 | |||||||
chr6:155304222 | C | A | 4 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-5637G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304222 | |||||||
chr6:155304276 | C | G | 2 | a0001c0001t0004g0164 a0001c0001t0004g0176 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.286-5691G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304276 | |||||||
chr6:155304288 | A | G | 1 | a0001c0002t0010g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-5703T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304288 | |||||||
chr6:155304411 | G | A | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-5826C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304411 | |||||||
chr6:155304424 | T | A | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-5839A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304424 | |||||||
chr6:155304599 | G | A | 3 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0003g0003 |
6 | HG00733.hp1 HG01106.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-6014C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304599 | |||||||
chr6:155304679 | G | A | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-6094C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304679 | |||||||
chr6:155304737 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.286-6152G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304737 | |||||||
chr6:155304862 | C | A | 1 | a0001c0001t0008g0124 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-6277G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304862 | |||||||
chr6:155304891 | T | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01243.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.285+6297A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304891 | |||||||
chr6:155305117 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.285+6071A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305117 | |||||||
chr6:155305122 | ATATACAT others(141): Show |
A | 1 | a0001c0001t0028g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+5918_285+6065d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305122 | |||||||
chr6:155305123 | TATAC | T | 66 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(63): Show |
73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.285+6061_285+6064d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305123 | |||||||
chr6:155305127 | C | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6061G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305127 | |||||||
chr6:155305131 | A | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6057T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305131 | |||||||
chr6:155305132 | T | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6056A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305132 | |||||||
chr6:155305136 | A | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6052T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305136 | |||||||
chr6:155305137 | T | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6051A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305137 | |||||||
chr6:155305139 | T | A | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6049A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305139 | |||||||
chr6:155305140 | TTA | T | 65 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(62): Show |
72 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.285+6046_285+6047d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305140 | |||||||
chr6:155305146 | ATATAAAT others(43): Show |
A | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285+5992_285+6041d others(52): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305146 | |||||||
chr6:155305148 | A | T | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6040T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305148 | |||||||
chr6:155305151 | A | C | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6037T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305151 | |||||||
chr6:155305156 | A | G | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+6032T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305156 | |||||||
chr6:155305172 | TTA | T | 4 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0010g0058 others(1): Show |
4 | HG03490.hp2 NA18965.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+6014_285+6015d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305172 | |||||||
chr6:155305173 | T | TAC | 10 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(7): Show |
11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+6014_285+6015i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305173 | |||||||
chr6:155305174 | ATATATAT others(15): Show |
A | 43 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(40): Show |
49 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.285+5992_285+6013d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305174 | |||||||
chr6:155305175 | T | C | 12 | a0001c0001t0002g0289 a0001c0001t0013g0029 a0001c0001t0013g0030 others(9): Show |
12 | HG00621.hp1 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+6013A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305175 | |||||||
chr6:155305177 | TATATATT others(125): Show |
T | 1 | a0001c0001t0006g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285+5879_285+6010d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305177 | |||||||
chr6:155305178 | ATATATTA others(85): Show |
A | 1 | a0001c0002t0007g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285+5918_285+6009d others(94): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305178 | |||||||
chr6:155305179 | T | TATAA | 3 | a0001c0002t0006g0054 a0001c0002t0014g0053 a0001c0002t0029g0027 |
3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6008_285+6009i others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305179 | |||||||
chr6:155305180 | ATATTAAA others(9): Show |
A | 1 | a0001c0002t0003g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.285+5992_285+6007d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305180 | |||||||
chr6:155305190 | ATATATTT others(157): Show |
A | 1 | a0001c0001t0014g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+5834_285+5997d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305190 | |||||||
chr6:155305196 | TTATATAT others(69): Show |
T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(35): Show |
42 | HG00280.hp2 HG00673.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.285+5916_285+5991d others(78): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305196 | |||||||
chr6:155305196 | TTATATAT others(71): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.285+5914_285+5991d others(80): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305196 | |||||||
chr6:155305197 | T | C | 43 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(40): Show |
49 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.285+5991A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305197 | |||||||
chr6:155305197 | T | TAC | 16 | a0001c0001t0002g0289 a0001c0001t0012g0025 a0001c0001t0012g0256 others(13): Show |
17 | HG00621.hp1 HG00639.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+5990_285+5991i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305197 | |||||||
chr6:155305198 | ATATATAT others(65): Show |
A | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5918_285+5989d others(74): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305198 | |||||||
chr6:155305199 | T | A | 2 | a0001c0001t0016g0265 a0001c0002t0003g0204 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.285+5989A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305199 | |||||||
chr6:155305199 | T | C | 2 | a0001c0002t0006g0215 a0001c0002t0006g0216 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.285+5989A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305199 | |||||||
chr6:155305200 | ATATATAT others(13): Show |
A | 1 | a0001c0002t0004g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.285+5968_285+5987d others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305200 | |||||||
chr6:155305201 | TATATATT others(101): Show |
T | 1 | a0001c0002t0003g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+5879_285+5986d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305201 | |||||||
chr6:155305202 | ATATATTA others(11): Show |
A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0137 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.285+5968_285+5985d others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305202 | |||||||
chr6:155305212 | T | A | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5976A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305212 | |||||||
chr6:155305214 | ATATATTT others(133): Show |
A | 5 | a0001c0001t0004g0171 a0001c0001t0004g0211 a0001c0001t0014g0217 others(2): Show |
5 | HG02273.hp2 HG02965.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5834_285+5973d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305214 | |||||||
chr6:155305214 | ATATATTT others(165): Show |
A | 13 | a0001c0001t0001g0165 a0001c0001t0004g0164 a0001c0001t0004g0166 others(10): Show |
13 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+5802_285+5973d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305214 | |||||||
chr6:155305217 | T | A | 1 | a0001c0001t0013g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.285+5971A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305217 | |||||||
chr6:155305220 | T | TTA | 5 | a0001c0001t0030g0051 a0001c0002t0005g0008 a0001c0002t0005g0237 others(2): Show |
6 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5966_285+5967d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305220 | |||||||
chr6:155305220 | TTA | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0008g0002 others(16): Show |
22 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(19): Show |
intron_variant | MODIFIER | c.285+5966_285+5967d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305220 | |||||||
chr6:155305220 | TTATATAT others(45): Show |
T | 1 | a0001c0001t0008g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.285+5916_285+5967d others(54): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305220 | |||||||
chr6:155305221 | T | A | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5967A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305221 | |||||||
chr6:155305221 | T | TAC | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5966_285+5967i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305221 | |||||||
chr6:155305222 | A | C | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.285+5966T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305222 | |||||||
chr6:155305222 | ATATATAT others(41): Show |
A | 5 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0259 others(2): Show |
6 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5918_285+5965d others(50): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305222 | |||||||
chr6:155305223 | T | A | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5965A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305223 | |||||||
chr6:155305223 | T | C | 44 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(41): Show |
50 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.285+5965A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305223 | |||||||
chr6:155305224 | A | T | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5964T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305224 | |||||||
chr6:155305225 | T | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0137 a0001c0002t0004g0130 |
3 | HG02965.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.285+5963A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305225 | |||||||
chr6:155305225 | T | TATATAA | 16 | a0001c0001t0001g0068 a0001c0001t0001g0125 a0001c0001t0001g0127 others(13): Show |
18 | HG00735.hp2 HG01074.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.285+5962_285+5963i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305225 | |||||||
chr6:155305225 | TATATATA others(77): Show |
T | 1 | a0001c0002t0010g0181 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.285+5879_285+5962d others(86): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305225 | |||||||
chr6:155305226 | ATATATAT others(37): Show |
A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(74): Show |
86 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.285+5918_285+5961d others(46): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305226 | |||||||
chr6:155305229 | T | A | 10 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(7): Show |
10 | HG00639.hp1 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+5959A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305229 | |||||||
chr6:155305229 | T | TAA | 3 | a0001c0001t0002g0289 a0001c0002t0006g0215 a0001c0002t0006g0216 |
3 | HG00621.hp1 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.285+5958_285+5959i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305229 | |||||||
chr6:155305229 | TATATTA | T | 14 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5953_285+5958d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305229 | |||||||
chr6:155305238 | T | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5950A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305238 | |||||||
chr6:155305246 | T | A | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5942A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305246 | |||||||
chr6:155305246 | T | TTA | 3 | a0001c0002t0019g0024 a0001c0004t0020g0162 a0001c0004t0020g0163 |
4 | HG01256.hp1 HG01496.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5940_285+5941d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305246 | |||||||
chr6:155305246 | TTA | T | 5 | a0001c0002t0005g0009 a0001c0002t0010g0055 a0001c0002t0010g0056 others(2): Show |
5 | HG01358.hp1 HG03490.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+5940_285+5941d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305246 | |||||||
chr6:155305247 | T | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5941A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305247 | |||||||
chr6:155305248 | ATATATAT others(15): Show |
A | 37 | a0001c0001t0002g0004 a0001c0001t0002g0026 a0001c0001t0002g0232 others(34): Show |
41 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.285+5918_285+5939d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305248 | |||||||
chr6:155305249 | T | A | 15 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(12): Show |
20 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.285+5939A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | |||||||
chr6:155305249 | T | C | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285+5939A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | |||||||
chr6:155305249 | T | TATATATA others(1): Show |
23 | a0001c0001t0001g0068 a0001c0001t0001g0125 a0001c0001t0001g0128 others(20): Show |
25 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285+5938_285+5939i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | |||||||
chr6:155305249 | T | TATATATA others(33): Show |
1 | a0001c0001t0021g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285+5938_285+5939i others(42): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | |||||||
chr6:155305249 | T | TATATATA others(65): Show |
1 | a0001c0001t0001g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.285+5938_285+5939i others(74): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | |||||||
chr6:155305250 | A | T | 14 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5938T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305250 | |||||||
chr6:155305252 | ATATATTA others(11): Show |
A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0082 others(10): Show |
16 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+5918_285+5935d others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305252 | |||||||
chr6:155305253 | T | TATAA | 8 | a0001c0001t0002g0011 a0001c0001t0002g0274 a0001c0001t0002g0278 others(5): Show |
10 | HG00558.hp2 HG01433.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+5934_285+5935i others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305253 | |||||||
chr6:155305253 | T | TATAAATA others(53): Show |
1 | a0001c0002t0006g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.285+5934_285+5935i others(62): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305253 | |||||||
chr6:155305256 | ATTAAATT others(144): Show |
A | 1 | a0001c0001t0002g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5781_285+5931d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305256 | |||||||
chr6:155305258 | TAAATTA | T | 14 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5924_285+5929d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305258 | |||||||
chr6:155305270 | T | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0151 a0001c0001t0006g0218 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5918A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305270 | |||||||
chr6:155305271 | T | C | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5917A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305271 | |||||||
chr6:155305272 | A | T | 1 | a0001c0002t0007g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285+5916T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305272 | |||||||
chr6:155305273 | T | C | 1 | a0001c0001t0012g0257 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+5915A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305273 | |||||||
chr6:155305275 | T | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
122 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.285+5913A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305275 | |||||||
chr6:155305275 | T | TATAA | 3 | a0001c0001t0001g0127 a0001c0001t0001g0148 a0001c0001t0021g0035 |
3 | HG01074.hp1 HG04184.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.285+5912_285+5913i others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305275 | |||||||
chr6:155305275 | T | TATATAA | 26 | a0001c0001t0001g0068 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
28 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.285+5912_285+5913i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305275 | |||||||
chr6:155305277 | T | TATAAAC | 3 | a0001c0001t0001g0040 a0001c0004t0020g0162 a0001c0004t0020g0163 |
3 | HG02145.hp1 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5910_285+5911i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305277 | |||||||
chr6:155305277 | T | TATATATT others(25): Show |
1 | a0001c0001t0018g0249 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.285+5879_285+5910d others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305277 | |||||||
chr6:155305279 | T | A | 42 | a0001c0001t0002g0004 a0001c0001t0002g0026 a0001c0001t0002g0232 others(39): Show |
47 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.285+5909A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305279 | |||||||
chr6:155305279 | T | TAA | 8 | a0001c0001t0002g0011 a0001c0001t0002g0274 a0001c0001t0002g0278 others(5): Show |
10 | HG00558.hp2 HG01433.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+5908_285+5909i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305279 | |||||||
chr6:155305296 | TTA | T | 18 | a0001c0001t0001g0068 a0001c0001t0001g0128 a0001c0001t0001g0131 others(15): Show |
18 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.285+5890_285+5891d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305296 | |||||||
chr6:155305299 | T | C | 1 | a0001c0001t0028g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+5889A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305299 | |||||||
chr6:155305305 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0148 |
2 | HG01074.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.285+5883A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305305 | |||||||
chr6:155305307 | AACAT | A | 43 | a0001c0001t0002g0004 a0001c0001t0002g0026 a0001c0001t0002g0232 others(40): Show |
47 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.285+5877_285+5880d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305307 | |||||||
chr6:155305308 | A | T | 2 | a0001c0002t0006g0054 a0001c0002t0014g0053 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5880T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305308 | |||||||
chr6:155305309 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.285+5879G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305309 | |||||||
chr6:155305322 | A | ATATATTT others(25): Show |
1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+5865_285+5866i others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305322 | |||||||
chr6:155305322 | ATATATTT others(25): Show |
A | 1 | a0001c0002t0005g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.285+5834_285+5865d others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305322 | |||||||
chr6:155305328 | TTA | T | 29 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0069 others(26): Show |
32 | HG00609.hp2 HG00639.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.285+5858_285+5859d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305328 | |||||||
chr6:155305331 | TATATATA others(1): Show |
T | 4 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0001c0002t0029g0027 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5849_285+5856d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305331 | |||||||
chr6:155305334 | ATATAAAT others(172): Show |
A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5675_285+5853d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305334 | |||||||
chr6:155305337 | T | A | 8 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG00735.hp2 HG01074.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+5851A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305337 | |||||||
chr6:155305344 | A | AT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0123 a0001c0001t0009g0108 |
3 | HG03831.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.285+5843dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305344 | |||||||
chr6:155305352 | TTGTA | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0273 a0001c0001t0002g0275 others(1): Show |
6 | NA18967.hp1 NA18974.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5832_285+5835d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305352 | |||||||
chr6:155305354 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(224): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.285+5834C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305354 | |||||||
chr6:155305360 | T | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0273 a0001c0001t0002g0275 others(1): Show |
7 | NA18967.hp1 NA18969.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5828A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305360 | |||||||
chr6:155305360 | TTA | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(139): Show |
158 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.285+5826_285+5827d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305360 | |||||||
chr6:155305368 | ATAAATAT others(4): Show |
A | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5809_285+5819d others(13): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305368 | |||||||
chr6:155305369 | T | A | 11 | a0001c0001t0001g0069 a0001c0001t0001g0125 a0001c0001t0001g0133 others(8): Show |
13 | HG01099.hp1 HG01433.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.285+5819A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305369 | |||||||
chr6:155305371 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.285+5817T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305371 | |||||||
chr6:155305376 | A | AT | 4 | a0001c0002t0004g0005 a0001c0002t0004g0046 a0001c0002t0023g0047 others(1): Show |
6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5811dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305376 | |||||||
chr6:155305381 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285+5807T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305381 | |||||||
chr6:155305383 | A | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0290 |
4 | HG01433.hp1 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5805T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305383 | |||||||
chr6:155305384 | TTGTATA | T | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5798_285+5803d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305384 | |||||||
chr6:155305386 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.285+5802C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305386 | |||||||
chr6:155305392 | T | A | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5796A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305392 | |||||||
chr6:155305392 | TTA | T | 104 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0078 others(101): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.285+5794_285+5795d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305392 | |||||||
chr6:155305394 | A | ATATATAA others(21): Show |
5 | a0001c0001t0006g0007 a0001c0001t0006g0226 a0001c0001t0006g0227 others(2): Show |
7 | HG01891.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5793_285+5794i others(30): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305394 | |||||||
chr6:155305395 | TATATATA others(34): Show |
T | 2 | a0001c0001t0001g0128 a0001c0001t0009g0129 |
2 | HG02056.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.285+5752_285+5792d others(43): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305395 | |||||||
chr6:155305398 | ATATAAAT others(108): Show |
A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0290 |
4 | HG01433.hp1 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5675_285+5789d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305398 | |||||||
chr6:155305400 | ATAAATAT others(2): Show |
A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0001g0143 others(2): Show |
5 | HG01074.hp1 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5779_285+5787d others(11): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305400 | |||||||
chr6:155305401 | T | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
105 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.285+5787A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305401 | |||||||
chr6:155305402 | A | ATTAAATT others(7): Show |
2 | a0001c0002t0006g0054 a0001c0002t0014g0053 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5785_285+5786i others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305402 | |||||||
chr6:155305403 | A | T | 2 | a0001c0002t0006g0054 a0001c0002t0014g0053 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5785T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305403 | |||||||
chr6:155305408 | AT | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(245): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.285+5779delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305408 | |||||||
chr6:155305409 | T | A | 1 | a0001c0001t0002g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5779A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305409 | |||||||
chr6:155305409 | T | TATTAAAT others(24): Show |
1 | a0001c0001t0030g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+5778_285+5779i others(33): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305409 | |||||||
chr6:155305416 | A | G | 1 | a0001c0001t0002g0274 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.285+5772T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305416 | |||||||
chr6:155305419 | A | G | 1 | a0001c0002t0005g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.285+5769T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305419 | |||||||
chr6:155305424 | TTTATATA others(49): Show |
T | 1 | a0001c0001t0001g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.285+5708_285+5763d others(58): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305424 | |||||||
chr6:155305425 | TTA | T | 19 | a0001c0001t0001g0062 a0001c0001t0001g0076 a0001c0001t0001g0145 others(16): Show |
20 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+5761_285+5762d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305425 | |||||||
chr6:155305428 | TATATATA others(1): Show |
T | 31 | a0001c0001t0001g0069 a0001c0001t0001g0125 a0001c0001t0001g0131 others(28): Show |
31 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.285+5752_285+5759d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305428 | |||||||
chr6:155305431 | A | ATAAATAT others(9): Show |
1 | a0001c0001t0021g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285+5756_285+5757i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305431 | |||||||
chr6:155305433 | A | ATATTAAA others(9): Show |
2 | a0001c0002t0006g0054 a0001c0002t0014g0053 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5754_285+5755i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305433 | |||||||
chr6:155305434 | T | A | 101 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0078 others(98): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.285+5754A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305434 | |||||||
chr6:155305436 | A | AATATATA others(17): Show |
1 | a0001c0004t0020g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.285+5728_285+5751d others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305436 | |||||||
chr6:155305436 | A | T | 3 | a0001c0001t0021g0035 a0001c0002t0006g0054 a0001c0002t0014g0053 |
3 | HG02922.hp1 HG03471.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.285+5752T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305436 | |||||||
chr6:155305448 | A | G | 38 | a0001c0001t0002g0004 a0001c0001t0002g0026 a0001c0001t0002g0232 others(35): Show |
42 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.285+5740T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305448 | |||||||
chr6:155305456 | T | TATAAATA others(9): Show |
4 | a0001c0002t0004g0005 a0001c0002t0004g0046 a0001c0002t0023g0047 others(1): Show |
6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5731_285+5732i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305456 | |||||||
chr6:155305457 | TTA | T | 19 | a0001c0001t0002g0289 a0001c0001t0012g0025 a0001c0001t0012g0256 others(16): Show |
20 | HG00621.hp1 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+5729_285+5730d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305457 | |||||||
chr6:155305457 | TTATATAT others(75): Show |
T | 10 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(7): Show |
10 | HG00609.hp1 HG00738.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+5649_285+5730d others(84): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305457 | |||||||
chr6:155305460 | TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0149 a0001c0001t0006g0174 others(1): Show |
4 | HG01074.hp1 HG02155.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5720_285+5727d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305460 | |||||||
chr6:155305463 | A | ATAAATAT others(9): Show |
3 | a0001c0001t0013g0036 a0001c0001t0021g0037 a0001c0002t0004g0031 |
3 | HG00639.hp1 HG02647.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.285+5724_285+5725i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305463 | |||||||
chr6:155305463 | ATATAAAT others(43): Show |
A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0273 a0001c0001t0002g0275 others(1): Show |
7 | NA18967.hp1 NA18969.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5675_285+5724d others(52): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305463 | |||||||
chr6:155305463 | ATATAAAT others(99): Show |
A | 23 | a0001c0001t0002g0026 a0001c0001t0002g0232 a0001c0001t0002g0263 others(20): Show |
24 | HG00735.hp1 HG03704.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.285+5619_285+5724d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305463 | |||||||
chr6:155305465 | A | T | 4 | a0001c0002t0004g0005 a0001c0002t0004g0046 a0001c0002t0023g0047 others(1): Show |
6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5723T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305465 | |||||||
chr6:155305466 | T | A | 55 | a0001c0001t0001g0076 a0001c0001t0006g0007 a0001c0001t0006g0218 others(52): Show |
65 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.285+5722A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305466 | |||||||
chr6:155305467 | A | ATT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
100 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.285+5720_285+5721i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305467 | |||||||
chr6:155305467 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.285+5721T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305467 | |||||||
chr6:155305468 | A | T | 7 | a0001c0001t0013g0036 a0001c0001t0021g0037 a0001c0002t0004g0005 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5720T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305468 | |||||||
chr6:155305468 | AATATATA others(97): Show |
A | 1 | a0001c0001t0002g0274 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.285+5616_285+5719d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305468 | |||||||
chr6:155305470 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(84): Show |
101 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.285+5718A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305470 | |||||||
chr6:155305471 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(85): Show |
102 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.285+5717T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305471 | |||||||
chr6:155305473 | A | AT | 5 | a0001c0002t0004g0039 a0001c0002t0004g0049 a0001c0002t0010g0048 others(2): Show |
5 | HG02647.hp1 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+5714dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305473 | |||||||
chr6:155305474 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285+5714A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305474 | |||||||
chr6:155305476 | TTA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(84): Show |
101 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.285+5710_285+5711d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305476 | |||||||
chr6:155305479 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285+5709T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305479 | |||||||
chr6:155305480 | A | ATTATATA others(1): Show |
25 | a0001c0001t0001g0076 a0001c0001t0001g0141 a0001c0001t0001g0144 others(22): Show |
32 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.285+5700_285+5707d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305480 | |||||||
chr6:155305480 | A | ATTATATA others(49): Show |
3 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0005g0250 |
3 | HG02486.hp1 HG02717.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.285+5652_285+5707d others(58): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305480 | |||||||
chr6:155305480 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(84): Show |
101 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.285+5708T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305480 | |||||||
chr6:155305483 | A | ATATATT | 8 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(5): Show |
9 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5704_285+5705i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305483 | |||||||
chr6:155305483 | A | T | 2 | a0001c0001t0001g0080 a0001c0002t0006g0216 |
2 | HG02486.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.285+5705T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305483 | |||||||
chr6:155305486 | T | C | 10 | a0001c0001t0015g0205 a0001c0002t0007g0020 a0001c0002t0007g0059 others(7): Show |
11 | HG02040.hp1 HG02071.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+5702A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305486 | |||||||
chr6:155305487 | A | ATT | 3 | a0001c0001t0024g0229 a0001c0001t0024g0230 a0004c0006t0038g0231 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5700_285+5701i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305487 | |||||||
chr6:155305487 | A | G | 1 | a0001c0002t0022g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.285+5701T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305487 | |||||||
chr6:155305488 | TATAAATA others(9): Show |
T | 2 | a0001c0001t0002g0289 a0001c0001t0016g0265 |
2 | HG00621.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.285+5684_285+5699d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305488 | |||||||
chr6:155305489 | A | T | 85 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0077 others(82): Show |
91 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.285+5699T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305489 | |||||||
chr6:155305490 | TAA | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0149 a0001c0001t0006g0174 |
3 | HG01074.hp1 HG02155.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.285+5696_285+5697d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305490 | |||||||
chr6:155305492 | A | AATATATA others(41): Show |
3 | a0001c0002t0005g0008 a0001c0002t0005g0237 a0001c0002t0005g0245 |
5 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+5648_285+5695d others(50): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305492 | |||||||
chr6:155305492 | A | T | 90 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0077 others(87): Show |
96 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.285+5696T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305492 | |||||||
chr6:155305494 | TA | T | 5 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(2): Show |
5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5693delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305494 | |||||||
chr6:155305498 | T | A | 5 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(2): Show |
5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5690A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305498 | |||||||
chr6:155305502 | A | ATAT | 5 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(2): Show |
5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5685_285+5686i others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305502 | |||||||
chr6:155305504 | A | T | 5 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(2): Show |
5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5684T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305504 | |||||||
chr6:155305513 | T | A | 5 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(2): Show |
5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5675A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305513 | |||||||
chr6:155305513 | TTA | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0126 others(30): Show |
34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.285+5673_285+5674d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305513 | |||||||
chr6:155305516 | T | A | 16 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0273 others(13): Show |
21 | HG00558.hp2 HG00621.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.285+5672A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305516 | |||||||
chr6:155305516 | T | TATATAA | 9 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(6): Show |
10 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+5671_285+5672i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305516 | |||||||
chr6:155305516 | T | TATATATA others(1): Show |
8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0006g0174 others(5): Show |
8 | HG00639.hp1 HG02155.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+5671_285+5672i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305516 | |||||||
chr6:155305519 | A | G | 41 | a0001c0001t0015g0205 a0001c0002t0003g0006 a0001c0002t0003g0021 others(38): Show |
46 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.285+5669T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305519 | |||||||
chr6:155305523 | ATT | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5663_285+5664d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305523 | |||||||
chr6:155305528 | A | T | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5660T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305528 | |||||||
chr6:155305529 | T | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5659A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305529 | |||||||
chr6:155305532 | T | A | 2 | a0001c0001t0024g0229 a0001c0001t0024g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.285+5656A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305532 | |||||||
chr6:155305534 | T | TTA | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5653_285+5654i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305534 | |||||||
chr6:155305536 | T | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5652A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305536 | |||||||
chr6:155305537 | T | A | 2 | a0001c0001t0024g0229 a0001c0001t0024g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.285+5651A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305537 | |||||||
chr6:155305537 | TTA | T | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG00558.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5649_285+5650d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305537 | |||||||
chr6:155305537 | TTATATAT others(27): Show |
T | 1 | a0001c0002t0022g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.285+5617_285+5650d others(36): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305537 | |||||||
chr6:155305538 | TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0127 |
2 | HG01074.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.285+5640_285+5649d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305538 | |||||||
chr6:155305539 | A | T | 5 | a0001c0001t0012g0025 a0001c0001t0012g0257 a0001c0001t0012g0259 others(2): Show |
6 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5649T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305539 | |||||||
chr6:155305539 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0031g0136 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.285+5619_285+5648d others(32): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305539 | |||||||
chr6:155305545 | A | T | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5643T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305545 | |||||||
chr6:155305546 | T | A | 1 | a0001c0001t0002g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5642A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305546 | |||||||
chr6:155305547 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5641T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305547 | |||||||
chr6:155305548 | A | AATATATA others(41): Show |
3 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 |
3 | HG02451.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.285+5592_285+5639d others(50): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305548 | |||||||
chr6:155305548 | A | T | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5640T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305548 | |||||||
chr6:155305548 | AATATATA others(51): Show |
A | 1 | a0001c0001t0028g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+5582_285+5639d others(60): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305548 | |||||||
chr6:155305549 | ATATATAT others(13): Show |
A | 3 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0022g0057 |
3 | HG03490.hp2 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.285+5619_285+5638d others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305549 | |||||||
chr6:155305550 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5638A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305550 | |||||||
chr6:155305551 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5637T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305551 | |||||||
chr6:155305556 | TTA | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(80): Show |
96 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.285+5630_285+5631d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305556 | |||||||
chr6:155305556 | TTAA | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0123 a0001c0001t0009g0108 |
3 | HG03831.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.285+5629_285+5631d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305556 | |||||||
chr6:155305560 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5628T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305560 | |||||||
chr6:155305560 | A | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(80): Show |
96 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.285+5628T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305560 | |||||||
chr6:155305562 | TA | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0123 a0001c0001t0009g0108 |
3 | HG03831.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.285+5625delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305562 | |||||||
chr6:155305569 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5619A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | |||||||
chr6:155305569 | T | TTA | 11 | a0001c0001t0002g0004 a0001c0001t0002g0273 a0001c0001t0002g0275 others(8): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+5617_285+5618d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | |||||||
chr6:155305569 | T | TTATATAT others(27): Show |
1 | a0001c0002t0037g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285+5618_285+5619i others(36): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | |||||||
chr6:155305569 | TTA | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(43): Show |
51 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.285+5617_285+5618d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | |||||||
chr6:155305569 | TTATATAT others(53): Show |
T | 15 | a0001c0001t0001g0165 a0001c0001t0004g0164 a0001c0001t0004g0166 others(12): Show |
15 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+5559_285+5618d others(62): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | |||||||
chr6:155305570 | TATATATA others(25): Show |
T | 1 | a0001c0001t0016g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285+5586_285+5617d others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305570 | |||||||
chr6:155305571 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.285+5617T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305571 | |||||||
chr6:155305572 | T | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
122 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.285+5616A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | |||||||
chr6:155305572 | T | TATATAA | 4 | a0001c0001t0002g0289 a0001c0001t0006g0174 a0001c0002t0003g0197 others(1): Show |
4 | HG00621.hp1 HG02486.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5615_285+5616i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | |||||||
chr6:155305572 | T | TATATAAA others(1): Show |
3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5615_285+5616i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | |||||||
chr6:155305572 | T | TATATATA others(1): Show |
21 | a0001c0001t0001g0019 a0001c0001t0001g0068 a0001c0001t0001g0128 others(18): Show |
22 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.285+5615_285+5616i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | |||||||
chr6:155305576 | TATATTAA others(19): Show |
T | 16 | a0001c0001t0001g0069 a0001c0001t0001g0126 a0001c0001t0001g0131 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.285+5586_285+5611d others(28): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305576 | |||||||
chr6:155305579 | ATT | A | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(2): Show |
5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5607_285+5608d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305579 | |||||||
chr6:155305584 | A | G | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5604T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305584 | |||||||
chr6:155305584 | A | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(2): Show |
5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5604T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305584 | |||||||
chr6:155305585 | T | A | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(2): Show |
5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5603A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305585 | |||||||
chr6:155305590 | T | TTA | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(2): Show |
5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5597_285+5598i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305590 | |||||||
chr6:155305592 | T | A | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(2): Show |
5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5596A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305592 | |||||||
chr6:155305593 | T | TTA | 3 | a0001c0001t0001g0040 a0001c0001t0030g0051 a0001c0004t0020g0162 |
3 | HG02257.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5593_285+5594d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305593 | |||||||
chr6:155305593 | TTATATAT others(3): Show |
T | 1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5585_285+5594d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305593 | |||||||
chr6:155305593 | TTATATAT others(5): Show |
T | 12 | a0001c0001t0001g0076 a0001c0001t0006g0007 a0001c0001t0006g0218 others(9): Show |
17 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+5583_285+5594d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305593 | |||||||
chr6:155305597 | A | ATATATTA others(3): Show |
1 | a0001c0001t0006g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285+5590_285+5591i others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305597 | |||||||
chr6:155305600 | TAA | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
160 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.285+5586_285+5587d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305600 | |||||||
chr6:155305601 | A | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(2): Show |
5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5587T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305601 | |||||||
chr6:155305602 | A | T | 7 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0277 others(4): Show |
7 | HG00609.hp1 HG00738.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5586T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305602 | |||||||
chr6:155305602 | AATAT | A | 58 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0273 others(55): Show |
69 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.285+5582_285+5585d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305602 | |||||||
chr6:155305603 | A | ATATATAT others(13): Show |
1 | a0001c0002t0006g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285+5584_285+5585i others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305603 | |||||||
chr6:155305605 | A | T | 1 | a0001c0001t0006g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285+5583T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305605 | |||||||
chr6:155305606 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(157): Show |
176 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.285+5582A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305606 | |||||||
chr6:155305606 | T | TATATTAA others(53): Show |
2 | a0001c0001t0001g0040 a0001c0004t0020g0162 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5581_285+5582i others(62): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305606 | |||||||
chr6:155305627 | TTA | T | 64 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0266 others(61): Show |
75 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.285+5559_285+5560d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305627 | |||||||
chr6:155305630 | TATATATA others(1): Show |
T | 7 | a0001c0001t0002g0291 a0001c0001t0002g0293 a0001c0001t0025g0303 others(4): Show |
7 | HG00738.hp2 HG02683.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5550_285+5557d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305630 | |||||||
chr6:155305632 | TATATAA | T | 24 | a0001c0001t0002g0026 a0001c0001t0002g0232 a0001c0001t0002g0263 others(21): Show |
25 | HG00621.hp1 HG00735.hp1 HG03704.hp1 others(22): Show |
intron_variant | MODIFIER | c.285+5550_285+5555d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305632 | |||||||
chr6:155305656 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.285+5532A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305656 | |||||||
chr6:155305659 | TTA | T | 84 | a0001c0001t0002g0026 a0001c0001t0002g0232 a0001c0001t0002g0263 others(81): Show |
90 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.285+5527_285+5528d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305659 | |||||||
chr6:155305662 | TATATATA others(1): Show |
T | 3 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 |
3 | HG02622.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5518_285+5525d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305662 | |||||||
chr6:155305664 | TATATAA | T | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5518_285+5523d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305664 | |||||||
chr6:155305665 | ATATAAAT others(49): Show |
A | 6 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0273 others(3): Show |
11 | HG01433.hp1 HG02738.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+5467_285+5522d others(58): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305665 | |||||||
chr6:155305670 | AATATATA others(47): Show |
A | 1 | a0001c0001t0006g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285+5464_285+5517d others(56): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305670 | |||||||
chr6:155305683 | T | TA | 6 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5504_285+5505i others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305683 | |||||||
chr6:155305689 | A | T | 6 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5499T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305689 | |||||||
chr6:155305691 | T | A | 7 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(4): Show |
8 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+5497A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305691 | |||||||
chr6:155305691 | T | TTA | 184 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.285+5495_285+5496d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305691 | |||||||
chr6:155305694 | TATATAA | T | 10 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0036 others(7): Show |
10 | HG00639.hp1 HG01109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+5488_285+5493d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305694 | |||||||
chr6:155305697 | A | ATATATTA others(11): Show |
3 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0002t0010g0034 |
3 | HG02723.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.285+5490_285+5491i others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305697 | |||||||
chr6:155305697 | A | ATATATTA others(35): Show |
1 | a0001c0002t0029g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5490_285+5491i others(44): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305697 | |||||||
chr6:155305699 | AAATATAT others(15): Show |
A | 1 | a0001c0001t0014g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+5467_285+5488d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305699 | |||||||
chr6:155305700 | A | T | 4 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0002t0010g0034 others(1): Show |
4 | HG02723.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5488T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305700 | |||||||
chr6:155305712 | AT | A | 10 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(7): Show |
11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+5475delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305712 | |||||||
chr6:155305721 | T | A | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5467A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305721 | |||||||
chr6:155305721 | TTA | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(175): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.285+5465_285+5466d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305721 | |||||||
chr6:155305724 | T | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0273 others(6): Show |
14 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.285+5464A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305724 | |||||||
chr6:155305724 | T | TATATAA | 37 | a0001c0001t0002g0026 a0001c0001t0002g0232 a0001c0001t0002g0263 others(34): Show |
38 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.285+5463_285+5464i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305724 | |||||||
chr6:155305747 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285+5441T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305747 | |||||||
chr6:155305820 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.285+5368T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305820 | |||||||
chr6:155305875 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.285+5313A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305875 | |||||||
chr6:155305908 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5280A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305908 | |||||||
chr6:155305947 | C | T | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5241G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305947 | |||||||
chr6:155306029 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.285+5159T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306029 | |||||||
chr6:155306096 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(252): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.285+5092C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306096 | |||||||
chr6:155306198 | A | G | 70 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(67): Show |
77 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.285+4990T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306198 | |||||||
chr6:155306226 | T | C | 70 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(67): Show |
77 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.285+4962A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306226 | |||||||
chr6:155306296 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.285+4892G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306296 | |||||||
chr6:155306303 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.285+4885T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306303 | |||||||
chr6:155306394 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0144 |
2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.285+4794C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306394 | |||||||
chr6:155306501 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.285+4687G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306501 | |||||||
chr6:155306696 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285+4492C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306696 | |||||||
chr6:155306843 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.285+4345C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306843 | |||||||
chr6:155307136 | T | TAC | 9 | a0001c0001t0002g0263 a0001c0001t0017g0251 a0001c0002t0005g0010 others(6): Show |
10 | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+4050_285+4051d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | T | TACAC | 5 | a0001c0001t0002g0266 a0001c0001t0016g0265 a0001c0002t0006g0054 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+4048_285+4051d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | T | TACACAC | 10 | a0001c0001t0002g0232 a0001c0001t0002g0267 a0001c0001t0002g0268 others(7): Show |
10 | HG00609.hp1 HG00735.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+4046_285+4051d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | T | TACACACA others(1): Show |
20 | a0001c0001t0002g0004 a0001c0001t0002g0026 a0001c0001t0002g0273 others(17): Show |
24 | HG00558.hp2 HG00621.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.285+4044_285+4051d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | T | TACACACA others(3): Show |
15 | a0001c0001t0002g0011 a0001c0001t0002g0290 a0001c0001t0002g0291 others(12): Show |
17 | HG00738.hp2 HG01433.hp1 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+4042_285+4051d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | T | TACATACA others(7): Show |
2 | a0001c0001t0024g0229 a0001c0001t0024g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.285+4051_285+4052i others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | TAC | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG00099.hp1 HG00738.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+4050_285+4051d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307136 | TACAC | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(165): Show |
193 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.285+4048_285+4051d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | |||||||
chr6:155307138 | C | CACACACA others(1): Show |
9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+4049_285+4050i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307138 | |||||||
chr6:155307166 | CAT | C | 6 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+4020_285+4021d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307166 | |||||||
chr6:155307168 | T | C | 60 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(57): Show |
66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.285+4020A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307168 | |||||||
chr6:155307273 | G | A | 2 | a0001c0002t0004g0005 a0003c0007t0032g0052 |
4 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+3915C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307273 | |||||||
chr6:155307323 | A | C | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+3865T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307323 | |||||||
chr6:155307409 | G | A | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3779C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307409 | |||||||
chr6:155307574 | C | T | 66 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(63): Show |
73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.285+3614G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307574 | |||||||
chr6:155307667 | T | G | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3521A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307667 | |||||||
chr6:155307688 | C | T | 1 | a0004c0006t0038g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285+3500G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307688 | |||||||
chr6:155307713 | C | T | 1 | a0001c0002t0035g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+3475G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307713 | |||||||
chr6:155307863 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.285+3325C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307863 | |||||||
chr6:155307909 | GA | G | 59 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(56): Show |
66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.285+3278delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307909 | |||||||
chr6:155307965 | A | C | 6 | a0001c0001t0012g0025 a0001c0001t0012g0256 a0001c0001t0012g0257 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3223T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307965 | |||||||
chr6:155308014 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.285+3174A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308014 | |||||||
chr6:155308244 | A | G | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+2944T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308244 | |||||||
chr6:155308323 | C | T | 2 | a0001c0001t0025g0303 a0001c0001t0025g0304 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.285+2865G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308323 | |||||||
chr6:155308345 | C | A | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+2843G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308345 | |||||||
chr6:155308474 | C | T | 1 | a0001c0002t0014g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+2714G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308474 | |||||||
chr6:155308544 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
124 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.285+2644A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308544 | |||||||
chr6:155308851 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(251): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.285+2337G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308851 | |||||||
chr6:155309106 | G | GA | 4 | a0001c0001t0001g0214 a0001c0002t0010g0056 a0001c0002t0010g0058 others(1): Show |
4 | NA18956.hp1 NA18965.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+2081dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309106 | |||||||
chr6:155309188 | G | A | 1 | a0001c0001t0034g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.285+2000C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309188 | |||||||
chr6:155309265 | A | G | 1 | a0001c0002t0003g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+1923T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309265 | |||||||
chr6:155309288 | T | C | 2 | a0001c0001t0002g0301 a0001c0001t0016g0302 |
2 | NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.285+1900A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309288 | |||||||
chr6:155309519 | G | A | 42 | a0001c0001t0015g0205 a0001c0002t0003g0006 a0001c0002t0003g0021 others(39): Show |
47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.285+1669C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309519 | |||||||
chr6:155309608 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+1580C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309608 | |||||||
chr6:155309678 | A | G | 4 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1510T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309678 | |||||||
chr6:155309686 | G | A | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1502C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309686 | |||||||
chr6:155309908 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+1280G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309908 | |||||||
chr6:155310208 | A | G | 2 | a0001c0001t0028g0028 a0001c0002t0029g0027 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.285+980T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310208 | |||||||
chr6:155310655 | C | T | 2 | a0001c0002t0006g0215 a0001c0002t0006g0216 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.285+533G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310655 | |||||||
chr6:155310686 | C | G | 2 | a0001c0004t0020g0162 a0001c0004t0020g0163 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+502G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310686 | |||||||
chr6:155310842 | C | T | 2 | a0001c0001t0006g0218 a0001c0001t0006g0219 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.285+346G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310842 | |||||||
chr6:155310906 | T | TA | 43 | a0001c0001t0004g0176 a0001c0001t0015g0205 a0001c0002t0003g0006 others(40): Show |
48 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.285+281dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310906 | |||||||
chr6:155310956 | A | C | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+232T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310956 | |||||||
chr6:155310999 | T | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG01168.hp2 HG01175.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+189A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310999 | |||||||
chr6:155311125 | A | G | 4 | a0001c0001t0028g0028 a0001c0002t0006g0054 a0001c0002t0014g0053 others(1): Show |
4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+63T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155311125 | |||||||
chr6:155311363 | A | T | 1 | a0001c0001t0009g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.134-24T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311363 | |||||||
chr6:155311427 | C | A | 1 | a0001c0002t0003g0210 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.134-88G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311427 | |||||||
chr6:155311628 | T | C | 66 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(63): Show |
73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.134-289A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311628 | |||||||
chr6:155311710 | T | C | 59 | a0001c0001t0001g0165 a0001c0001t0004g0164 a0001c0001t0004g0166 others(56): Show |
64 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.134-371A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311710 | |||||||
chr6:155311804 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(249): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.134-465A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311804 | |||||||
chr6:155311816 | G | C | 1 | a0001c0001t0004g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.134-477C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311816 | |||||||
chr6:155311851 | A | G | 1 | a0001c0001t0021g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.134-512T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311851 | |||||||
chr6:155311853 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.134-514T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311853 | |||||||
chr6:155311871 | A | G | 4 | a0001c0002t0007g0020 a0001c0002t0007g0059 a0001c0002t0007g0160 others(1): Show |
5 | HG02129.hp1 HG02523.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-532T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311871 | |||||||
chr6:155311988 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0226 a0001c0001t0006g0227 others(1): Show |
6 | HG02280.hp1 HG02723.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-649A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311988 | |||||||
chr6:155312105 | T | C | 2 | a0001c0001t0004g0212 a0001c0001t0004g0213 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.134-766A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312105 | |||||||
chr6:155312200 | C | T | 2 | a0001c0002t0004g0039 a0001c0002t0023g0038 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-861G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312200 | |||||||
chr6:155312223 | G | A | 2 | a0001c0001t0025g0303 a0001c0001t0025g0304 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.134-884C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312223 | |||||||
chr6:155312334 | C | T | 9 | a0001c0001t0013g0029 a0001c0001t0013g0030 a0001c0001t0013g0032 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-995G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312334 | |||||||
chr6:155312774 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.134-1435T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312774 | |||||||
chr6:155312818 | T | C | 1 | a0001c0002t0005g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.133+1478A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312818 | |||||||
chr6:155312835 | G | A | 2 | a0001c0002t0005g0010 a0001c0002t0005g0262 |
3 | HG00280.hp1 HG01515.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.133+1461C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312835 | |||||||
chr6:155312858 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0061 others(9): Show |
14 | HG00609.hp2 HG02071.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.133+1438T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312858 | |||||||
chr6:155313018 | C | T | 1 | a0001c0002t0003g0003 | 4 | HG00733.hp1 HG01192.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1278G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313018 | |||||||
chr6:155313234 | T | C | 5 | a0001c0001t0001g0214 a0001c0002t0010g0055 a0001c0002t0010g0056 others(2): Show |
5 | HG03490.hp2 NA18956.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+1062A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313234 | |||||||
chr6:155313255 | GA | G | 11 | a0001c0001t0002g0263 a0001c0001t0013g0029 a0001c0001t0013g0030 others(8): Show |
11 | HG01109.hp1 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+1040delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313255 | |||||||
chr6:155313480 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(118): Show |
136 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.133+816G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313480 | |||||||
chr6:155313533 | T | C | 46 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0026 others(43): Show |
52 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+763A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313533 | |||||||
chr6:155313746 | C | T | 1 | a0001c0002t0007g0059 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.133+550G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313746 | |||||||
chr6:155313832 | G | A | 2 | a0001c0002t0006g0215 a0001c0002t0006g0216 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.133+464C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313832 | |||||||
chr6:155314028 | C | A | 1 | a0001c0001t0014g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.133+268G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314028 | |||||||
chr6:155314047 | T | C | 13 | a0001c0001t0006g0007 a0001c0001t0006g0218 a0001c0001t0006g0219 others(10): Show |
18 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.133+249A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314047 | |||||||
chr6:155314147 | G | GTTC | 189 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(186): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.133+146_133+148dup others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314147 | |||||||
chr6:155314172 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.133+124G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314172 | |||||||
chr6:155314261 | G | A | 1 | a0002c0005t0039g0305 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.133+35C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314261 |