Item | Value |
---|---|
geneid | 7045 |
ensemblid | ENSG00000120708.17 |
hgncid | 11771 |
symbol | TGFBI |
name | transforming growth factor beta induced |
refseq_nuc | NM_000358.3 |
refseq_prot | NP_000349.1 |
ensembl_nuc | ENST00000442011.7 |
ensembl_prot | ENSP00000416330.2 |
mane_status | MANE Select |
chr | chr5 |
start | 136028988 |
end | 136063818 |
strand | + |
ver | v1.2 |
region | chr5:136028988-136063818 |
region5000 | chr5:136023988-136068818 |
regionname0 | TGFBI_chr5_136028988_136063818 |
regionname5000 | TGFBI_chr5_136023988_136068818 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 683 | 393 | 89 | 58 | 188 | 16 | 40 | 150 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(678): Show |
chr5 | 136023988 | 136068818 |
a0002 | 0/0 | 683 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(678): Show |
chr5 | 136023988 | 136068818 |
a0003 | 0/0 | 683 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(678): Show |
chr5 | 136023988 | 136068818 |
a0004 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(678): Show |
chr5 | 136023988 | 136068818 |
a0005 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(644): Show |
chr5 | 136023988 | 136068818 |
a0006 | 0/0 | 683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(678): Show |
chr5 | 136023988 | 136068818 |
a0007 | 0/0 | 683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | MALFV others(678): Show |
chr5 | 136023988 | 136068818 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2049 | 113 | 26 | 16 | 54 | 3 | 14 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0002 | 0/1 | 2049 | 112 | 4 | 20 | 67 | 6 | 14 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0003 | 1/0 | 2049 | 96 | 18 | 14 | 47 | 7 | 9 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0004 | 0/0 | 2049 | 32 | 25 | 7 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0005 | 0/0 | 2049 | 16 | 7 | 0 | 9 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0006 | 0/0 | 2049 | 8 | 0 | 0 | 8 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0007 | 0/0 | 2049 | 7 | 6 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0010 | 0/0 | 2049 | 2 | 0 | 0 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0011 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0012 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0013 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0017 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0018 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0019 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0001c0021 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0002c0008 | 0/0 | 2049 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0003c0009 | 0/0 | 2049 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0004c0020 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0005c0016 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2060): Show |
chr5 | 136023988 | 136068818 | ||
a0006c0015 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 | ||
a0007c0014 | 0/0 | 2049 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | ATGGC others(2044): Show |
chr5 | 136023988 | 136068818 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2712 | 6 | 5 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0001t0002 | 0/0 | 2712 | 106 | 20 | 16 | 54 | 3 | 13 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0001t0003 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0002t0001 | 0/1 | 2712 | 112 | 4 | 20 | 67 | 6 | 14 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0003t0001 | 1/0 | 2712 | 67 | 14 | 12 | 28 | 7 | 5 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0003t0002 | 0/0 | 2712 | 29 | 4 | 2 | 19 | 0 | 4 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0004t0001 | 0/0 | 2712 | 7 | 2 | 5 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0004t0002 | 0/0 | 2712 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0004t0003 | 0/0 | 2712 | 21 | 19 | 2 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0005t0002 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0005t0004 | 0/0 | 2712 | 14 | 5 | 0 | 9 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0006t0001 | 0/0 | 2712 | 8 | 0 | 0 | 8 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0007t0001 | 0/0 | 2712 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0007t0002 | 0/0 | 2712 | 3 | 2 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0010t0002 | 0/0 | 2712 | 2 | 0 | 0 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0011t0001 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0012t0001 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0013t0001 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0017t0001 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0018t0004 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0019t0005 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0001c0021t0003 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0002c0008t0001 | 0/0 | 2712 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0003c0009t0001 | 0/0 | 2712 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0004c0020t0002 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0005c0016t0002 | 0/0 | 2728 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2723): Show |
chr5 | 136023988 | 136068818 |
a0006c0015t0001 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
a0007c0014t0002 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | CTCAC others(2707): Show |
chr5 | 136023988 | 136068818 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0002 | 0/0 | 29 | 0 | 3 | 20 | 2 | 4 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0006 | 0/0 | 8 | 1 | 0 | 5 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0008 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0060 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0061 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0001 | 0/0 | 50 | 1 | 8 | 32 | 0 | 9 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0003 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0021 | 0/1 | 3 | 0 | 0 | 0 | 1 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0005 | 0/0 | 8 | 0 | 5 | 2 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0026 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0028 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0059 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0004t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0005t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0006t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0007t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0007t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0007t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0007t0002g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0007t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0010t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0017t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0018t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0019t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0001c0021t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0002c0008t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0003c0009t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0004c0020t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0005c0016t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0006c0015t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
a0007c0014t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0035 | EUR | GBR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0038 | EUR | GBR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0035 | EUR | GBR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0135 | EUR | FIN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00673 | hp1 | a0001 | c0003 | t0002 | g0089 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | CHS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0059 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00741 | hp1 | a0001 | c0007 | t0002 | g0053 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01069 | hp2 | a0001 | c0004 | t0003 | g0052 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01071 | hp2 | a0001 | c0004 | t0003 | g0052 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0086 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0027 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0078 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0054 | EUR | IBS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0044 | EUR | IBS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0054 | EUR | IBS | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01884 | hp1 | a0001 | c0004 | t0003 | g0055 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01891 | hp1 | a0002 | c0008 | t0001 | g0012 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0034 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01993 | hp1 | a0001 | c0004 | t0001 | g0034 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0019 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02083 | hp1 | a0001 | c0005 | t0004 | g0057 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02083 | hp2 | a0003 | c0009 | t0001 | g0001 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02129 | hp2 | a0001 | c0005 | t0004 | g0014 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02132 | hp1 | a0004 | c0020 | t0002 | g0136 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02145 | hp1 | a0001 | c0007 | t0002 | g0053 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02155 | hp1 | a0001 | c0005 | t0004 | g0014 | EAS | CDX | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02155 | hp2 | a0001 | c0006 | t0001 | g0011 | EAS | CDX | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | CDX | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02165 | hp2 | a0001 | c0005 | t0004 | g0014 | EAS | CDX | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02280 | hp1 | a0001 | c0007 | t0002 | g0162 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0191 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0079 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02451 | hp1 | a0001 | c0004 | t0003 | g0170 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0152 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02523 | hp1 | a0001 | c0003 | t0002 | g0090 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0024 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02572 | hp2 | a0001 | c0004 | t0002 | g0151 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02602 | hp1 | a0001 | c0003 | t0002 | g0019 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0009 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02622 | hp2 | a0001 | c0007 | t0001 | g0123 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02698 | hp1 | a0001 | c0003 | t0002 | g0179 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02735 | hp2 | a0001 | c0003 | t0002 | g0059 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0019 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02809 | hp1 | a0001 | c0005 | t0004 | g0056 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02809 | hp2 | a0001 | c0004 | t0003 | g0009 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02818 | hp1 | a0002 | c0008 | t0001 | g0012 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02886 | hp1 | a0001 | c0004 | t0003 | g0009 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02886 | hp2 | a0001 | c0004 | t0003 | g0088 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02895 | hp1 | a0001 | c0005 | t0004 | g0025 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02896 | hp1 | a0001 | c0004 | t0002 | g0051 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02897 | hp1 | a0001 | c0004 | t0002 | g0051 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02922 | hp1 | a0002 | c0008 | t0001 | g0012 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02922 | hp2 | a0001 | c0005 | t0004 | g0190 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02965 | hp1 | a0001 | c0017 | t0001 | g0164 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0167 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02970 | hp2 | a0001 | c0004 | t0003 | g0045 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02976 | hp2 | a0001 | c0004 | t0003 | g0047 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0038 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03130 | hp1 | a0001 | c0004 | t0003 | g0024 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03130 | hp2 | a0001 | c0005 | t0002 | g0172 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03139 | hp1 | a0001 | c0004 | t0003 | g0055 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03139 | hp2 | a0001 | c0004 | t0003 | g0066 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0009 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03209 | hp1 | a0001 | c0005 | t0004 | g0025 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03209 | hp2 | a0005 | c0016 | t0002 | g0098 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03225 | hp1 | a0001 | c0007 | t0001 | g0122 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03239 | hp2 | a0001 | c0012 | t0001 | g0001 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03453 | hp1 | a0001 | c0003 | t0002 | g0093 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03453 | hp2 | a0001 | c0021 | t0003 | g0045 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0075 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03490 | hp1 | a0001 | c0010 | t0002 | g0002 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03490 | hp2 | a0006 | c0015 | t0001 | g0175 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0036 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03492 | hp1 | a0001 | c0010 | t0002 | g0002 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0036 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03516 | hp1 | a0001 | c0007 | t0001 | g0121 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03516 | hp2 | a0002 | c0008 | t0001 | g0012 | AFR | ESN | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03540 | hp2 | a0001 | c0004 | t0003 | g0047 | AFR | GWD | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03579 | hp1 | a0001 | c0004 | t0003 | g0150 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03688 | hp2 | a0007 | c0014 | t0002 | g0134 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0096 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | BEB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0026 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | STU | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18522 | hp1 | a0001 | c0005 | t0002 | g0025 | AFR | YRI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18522 | hp2 | a0001 | c0004 | t0003 | g0024 | AFR | YRI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18747 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | CHB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | YRI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18939 | hp2 | a0001 | c0003 | t0002 | g0071 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18940 | hp1 | a0001 | c0006 | t0001 | g0166 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18940 | hp2 | a0001 | c0013 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18942 | hp1 | a0001 | c0011 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18949 | hp1 | a0001 | c0019 | t0005 | g0076 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18950 | hp1 | a0003 | c0009 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18952 | hp2 | a0001 | c0005 | t0004 | g0014 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18953 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18962 | hp1 | a0003 | c0009 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0081 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18967 | hp1 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18968 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18969 | hp2 | a0001 | c0006 | t0001 | g0174 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18971 | hp2 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18979 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18981 | hp1 | a0001 | c0005 | t0004 | g0173 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18984 | hp1 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18988 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19002 | hp2 | a0001 | c0005 | t0004 | g0057 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19005 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19012 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19030 | hp1 | a0001 | c0007 | t0001 | g0168 | AFR | LWK | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19030 | hp2 | a0001 | c0004 | t0003 | g0009 | AFR | LWK | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | LWK | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19056 | hp1 | a0001 | c0005 | t0004 | g0058 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19057 | hp1 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19058 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19060 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19065 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19068 | hp1 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19070 | hp2 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19080 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19083 | hp2 | a0001 | c0006 | t0001 | g0165 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19087 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA19091 | hp2 | a0001 | c0005 | t0004 | g0058 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20129 | hp1 | a0001 | c0004 | t0003 | g0009 | AFR | ASW | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ASW | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0080 | EUR | TSI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0040 | EUR | TSI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0005 | EUR | TSI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | TSI | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02559 | hp1 | a0001 | c0018 | t0004 | g0180 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03471 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG03471 | hp2 | a0001 | c0004 | t0003 | g0171 | AFR | MSL | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0176 | AFR | USA | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | USA | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA20300 | hp2 | a0001 | c0005 | t0004 | g0056 | AFR | USA | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | LWK | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0021 | REF | REF | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0028 | REF | REF | TGFBI_chr5_136023988_136068818 | TGFBI | chr5 | 136023988 | 136068818 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136046862 | C | G | 1 | a0004 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.471C>G | p.Asp157Glu | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 5/17 | 539/2712 | 471/2052 | 157/683 | chr5 | 136046862 | |||
chr5:136049523 | G | A | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.856G>A | p.Glu286Lys | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/17 | 924/2712 | 856/2052 | 286/683 | chr5 | 136049523 | |||
chr5:136054763 | C | T | 1 | a0003 | 3 | HG02083.hp2 NA18950.hp1 NA18962.hp1 |
missense_variant | MODERATE | c.1312C>T | p.His438Tyr | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/17 | 1380/2712 | 1312/2052 | 438/683 | chr5 | 136054763 | |||
chr5:136054857 | G | A | 1 | a0006 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1406G>A | p.Arg469His | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/17 | 1474/2712 | 1406/2052 | 469/683 | chr5 | 136054857 | |||
chr5:136055755 | C | G | 1 | a0002 | 4 | HG01891.hp1 HG02818.hp1 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1486C>G | p.Arg496Gly | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/17 | 1554/2712 | 1486/2052 | 496/683 | chr5 | 136055755 | |||
chr5:136060887 | G | GCCCCCCC others(9): Show |
1 | a0005 | 1 | HG03209.hp2 | frameshift_variant | HIGH | c.1857_1858insCCCCCC others(10): Show |
p.Ala620fs | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1926/2712 | 1858/2052 | 620/683 | chr5 | 136060887 | |||
chr5:136060888 | G | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1858G>C | p.Ala620Pro | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1926/2712 | 1858/2052 | 620/683 | chr5 | 136060888 | |||
chr5:136060891 | A | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1861A>C | p.Thr621Pro | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1929/2712 | 1861/2052 | 621/683 | chr5 | 136060891 | |||
chr5:136060894 | A | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1864A>C | p.Asn622His | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1932/2712 | 1864/2052 | 622/683 | chr5 | 136060894 | |||
chr5:136060895 | A | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1865A>C | p.Asn622Thr | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1933/2712 | 1865/2052 | 622/683 | chr5 | 136060895 | |||
chr5:136060897 | G | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1867G>C | p.Gly623Arg | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1935/2712 | 1867/2052 | 623/683 | chr5 | 136060897 | |||
chr5:136060898 | G | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1868G>C | p.Gly623Ala | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1936/2712 | 1868/2052 | 623/683 | chr5 | 136060898 | |||
chr5:136060900 | G | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1870G>C | p.Val624Leu | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1938/2712 | 1870/2052 | 624/683 | chr5 | 136060900 | |||
chr5:136060901 | T | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1871T>C | p.Val624Ala | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1939/2712 | 1871/2052 | 624/683 | chr5 | 136060901 | |||
chr5:136060903 | G | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1873G>C | p.Val625Leu | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1941/2712 | 1873/2052 | 625/683 | chr5 | 136060903 | |||
chr5:136060904 | T | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1874T>C | p.Val625Ala | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1942/2712 | 1874/2052 | 625/683 | chr5 | 136060904 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136029115 | G | C | 1 | a0001c0011 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.60G>C | p.Ala20Ala | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/17 | 128/2712 | 60/2052 | 20/683 | chr5 | 136029115 | |||
chr5:136033769 | C | T | 1 | a0001c0021 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.141C>T | p.Asn47Asn | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/17 | 209/2712 | 141/2052 | 47/683 | chr5 | 136033769 | |||
chr5:136047300 | G | C | 5 | a0001c0002 a0001c0011 a0001c0012 others(2): Show |
117 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(114): Show |
synonymous_variant | LOW | c.651G>C | p.Leu217Leu | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/17 | 719/2712 | 651/2052 | 217/683 | chr5 | 136047300 | |||
chr5:136049483 | C | T | 2 | a0001c0006 a0001c0010 |
10 | HG02155.hp2 HG03490.hp1 HG03492.hp1 others(7): Show |
synonymous_variant | LOW | c.816C>T | p.Asn272Asn | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/17 | 884/2712 | 816/2052 | 272/683 | chr5 | 136049483 | |||
chr5:136049519 | C | A | 1 | a0001c0012 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.852C>A | p.Ala284Ala | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/17 | 920/2712 | 852/2052 | 284/683 | chr5 | 136049519 | |||
chr5:136052974 | A | G | 8 | a0001c0001 a0001c0004 a0001c0005 others(5): Show |
174 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(171): Show |
synonymous_variant | LOW | c.981A>G | p.Val327Val | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 8/17 | 1049/2712 | 981/2052 | 327/683 | chr5 | 136052974 | |||
chr5:136055685 | C | T | 4 | a0001c0001 a0001c0010 a0004c0020 others(1): Show |
117 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(114): Show |
synonymous_variant | LOW | c.1416C>T | p.Leu472Leu | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/17 | 1484/2712 | 1416/2052 | 472/683 | chr5 | 136055685 | |||
chr5:136056737 | T | C | 11 | a0001c0001 a0001c0004 a0001c0005 others(8): Show |
183 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(180): Show |
synonymous_variant | LOW | c.1620T>C | p.Phe540Phe | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/17 | 1688/2712 | 1620/2052 | 540/683 | chr5 | 136056737 | |||
chr5:136059160 | C | T | 1 | a0001c0017 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1749C>T | p.Ile583Ile | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/17 | 1817/2712 | 1749/2052 | 583/683 | chr5 | 136059160 | |||
chr5:136059214 | G | A | 3 | a0001c0005 a0001c0006 a0001c0018 |
25 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(22): Show |
splice_region_variant&synonymous_variant | LOW | c.1803G>A | p.Leu601Leu | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/17 | 1871/2712 | 1803/2052 | 601/683 | chr5 | 136059214 | |||
chr5:136060848 | G | C | 1 | a0005c0016 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1818G>C | p.Val606Val | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1886/2712 | 1818/2052 | 606/683 | chr5 | 136060848 | |||
chr5:136060881 | C | T | 1 | a0001c0013 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.1851C>T | p.Asp617Asp | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1919/2712 | 1851/2052 | 617/683 | chr5 | 136060881 | |||
chr5:136060893 | A | C | 1 | a0005c0016 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1863A>C | p.Thr621Thr | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1931/2712 | 1863/2052 | 621/683 | chr5 | 136060893 | |||
chr5:136060896 | T | C | 1 | a0005c0016 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1866T>C | p.Asn622Asn | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1934/2712 | 1866/2052 | 622/683 | chr5 | 136060896 | |||
chr5:136060902 | G | C | 1 | a0005c0016 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1872G>C | p.Val624Val | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/17 | 1940/2712 | 1872/2052 | 624/683 | chr5 | 136060902 | |||
chr5:136061570 | G | A | 1 | a0001c0019 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1977G>A | p.Ala659Ala | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/17 | 2045/2712 | 1977/2052 | 659/683 | chr5 | 136061570 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136063493 | C | A | 3 | a0001c0001t0003 a0001c0004t0003 a0001c0021t0003 |
23 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*267C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 17/17 | 267 | chr5 | 136063493 | ||||||
chr5:136063637 | G | A | 1 | a0001c0019t0005 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 17/17 | 411 | chr5 | 136063637 | ||||||
chr5:136063684 | G | A | 2 | a0001c0005t0004 a0001c0018t0004 |
15 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*458G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 17/17 | 458 | chr5 | 136063684 | ||||||
chr5:136063763 | T | G | 9 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0002 others(6): Show |
149 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*537T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 17/17 | 537 | chr5 | 136063763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136029317 | A | G | 196 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(193): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.134+128A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136029317 | |||||||
chr5:136029440 | T | C | 194 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(191): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.134+251T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136029440 | |||||||
chr5:136029447 | G | T | 194 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(191): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.134+258G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136029447 | |||||||
chr5:136029747 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02074.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.134+558G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136029747 | |||||||
chr5:136029961 | G | C | 3 | a0001c0001t0002g0064 a0001c0002t0001g0065 a0001c0003t0001g0029 |
4 | NA18952.hp1 NA18990.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+772G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136029961 | |||||||
chr5:136030072 | G | A | 1 | a0001c0004t0003g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.134+883G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136030072 | |||||||
chr5:136030446 | C | T | 1 | a0001c0003t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.134+1257C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136030446 | |||||||
chr5:136030447 | G | A | 50 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0097 others(47): Show |
94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.134+1258G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136030447 | |||||||
chr5:136030795 | G | A | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+1606G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136030795 | |||||||
chr5:136030796 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0188 |
3 | HG01069.hp1 HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.134+1607C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136030796 | |||||||
chr5:136031364 | T | A | 1 | a0001c0003t0001g0030 | 2 | HG00597.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.134+2175T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031364 | |||||||
chr5:136031368 | A | G | 7 | a0001c0001t0002g0182 a0001c0002t0001g0003 a0001c0002t0001g0183 others(4): Show |
21 | HG00558.hp2 HG02027.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.134+2179A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031368 | |||||||
chr5:136031386 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.134+2197G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031386 | |||||||
chr5:136031462 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.134+2273G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031462 | |||||||
chr5:136031531 | G | A | 46 | a0001c0001t0002g0104 a0001c0001t0002g0182 a0001c0002t0001g0001 others(43): Show |
125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.135-2232G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031531 | |||||||
chr5:136031895 | A | G | 1 | a0001c0001t0002g0060 | 2 | HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.135-1868A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031895 | |||||||
chr5:136031914 | C | T | 48 | a0001c0001t0002g0104 a0001c0001t0002g0177 a0001c0001t0002g0178 others(45): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.135-1849C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136031914 | |||||||
chr5:136032024 | A | G | 1 | a0001c0006t0001g0174 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.135-1739A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032024 | |||||||
chr5:136032068 | C | T | 80 | a0001c0001t0001g0099 a0001c0001t0002g0163 a0001c0001t0003g0169 others(77): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.135-1695C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032068 | |||||||
chr5:136032256 | T | C | 75 | a0001c0001t0001g0099 a0001c0001t0002g0163 a0001c0001t0003g0169 others(72): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.135-1507T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032256 | |||||||
chr5:136032346 | T | G | 1 | a0001c0003t0002g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.135-1417T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032346 | |||||||
chr5:136032347 | G | T | 1 | a0001c0003t0002g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.135-1416G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032347 | |||||||
chr5:136032348 | A | G | 1 | a0001c0003t0002g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.135-1415A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032348 | |||||||
chr5:136032520 | C | T | 1 | a0001c0003t0001g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135-1243C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032520 | |||||||
chr5:136032745 | C | T | 9 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(6): Show |
16 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.135-1018C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032745 | |||||||
chr5:136032782 | T | A | 1 | a0001c0003t0002g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.135-981T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032782 | |||||||
chr5:136032813 | A | T | 1 | a0001c0004t0003g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135-950A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032813 | |||||||
chr5:136032850 | G | GTA | 19 | a0001c0001t0001g0099 a0001c0001t0003g0169 a0001c0004t0002g0167 others(16): Show |
35 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(32): Show |
intron_variant | MODIFIER | c.135-910_135-909dup others(2): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 136032850 | ||||||
chr5:136032914 | C | T | 3 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0170 |
8 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.135-849C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136032914 | |||||||
chr5:136033140 | A | G | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
12 | HG01243.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.135-623A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136033140 | |||||||
chr5:136033174 | C | G | 2 | a0001c0001t0001g0155 a0001c0001t0002g0154 |
2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.135-589C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136033174 | |||||||
chr5:136033207 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.135-556G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136033207 | |||||||
chr5:136033252 | A | C | 1 | a0001c0004t0003g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135-511A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 1/16 | chr5 | 136033252 | |||||||
chr5:136033903 | G | A | 1 | a0001c0003t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.233+42G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136033903 | |||||||
chr5:136033908 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.233+47C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136033908 | |||||||
chr5:136034047 | T | C | 1 | a0006c0015t0001g0175 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.233+186T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034047 | |||||||
chr5:136034121 | C | CGT | 13 | a0001c0001t0001g0099 a0001c0001t0002g0062 a0001c0001t0003g0169 others(10): Show |
18 | HG01978.hp2 HG02451.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.233+281_233+282dup others(2): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 136034121 | ||||||
chr5:136034441 | C | T | 1 | a0001c0002t0001g0043 | 2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.233+580C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034441 | |||||||
chr5:136034508 | T | C | 194 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(191): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.233+647T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034508 | |||||||
chr5:136034539 | T | C | 3 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0170 |
8 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+678T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034539 | |||||||
chr5:136034579 | A | C | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.233+718A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034579 | |||||||
chr5:136034628 | G | A | 1 | a0001c0003t0001g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.233+767G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034628 | |||||||
chr5:136034645 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.233+784T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034645 | |||||||
chr5:136034763 | G | A | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233+902G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034763 | |||||||
chr5:136034874 | A | T | 1 | a0001c0002t0001g0115 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.233+1013A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034874 | |||||||
chr5:136034892 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.233+1031C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136034892 | |||||||
chr5:136035216 | C | T | 1 | a0001c0003t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.233+1355C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035216 | |||||||
chr5:136035263 | A | G | 4 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0170 others(1): Show |
9 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+1402A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035263 | |||||||
chr5:136035269 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.233+1408A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035269 | |||||||
chr5:136035398 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.233+1537C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035398 | |||||||
chr5:136035409 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.233+1548G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035409 | |||||||
chr5:136035481 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.233+1620C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035481 | |||||||
chr5:136035493 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.233+1632C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035493 | |||||||
chr5:136035529 | G | A | 1 | a0001c0001t0002g0046 | 2 | NA18972.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.233+1668G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035529 | |||||||
chr5:136035618 | C | A | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.233+1757C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035618 | |||||||
chr5:136035624 | C | CA | 35 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(32): Show |
59 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.233+1782dupA | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 136035624 | ||||||
chr5:136035638 | A | G | 11 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0003g0045 others(8): Show |
14 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+1777A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035638 | |||||||
chr5:136035639 | A | G | 55 | a0001c0001t0002g0163 a0001c0002t0001g0032 a0001c0002t0001g0033 others(52): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.233+1778A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035639 | |||||||
chr5:136035678 | C | G | 5 | a0001c0004t0002g0167 a0001c0006t0001g0011 a0001c0006t0001g0165 others(2): Show |
9 | HG02155.hp2 HG02965.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+1817C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035678 | |||||||
chr5:136035686 | G | C | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.233+1825G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035686 | |||||||
chr5:136035884 | C | G | 12 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(9): Show |
15 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.233+2023C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035884 | |||||||
chr5:136035921 | G | T | 8 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(5): Show |
15 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.233+2060G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035921 | |||||||
chr5:136035938 | G | A | 9 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(6): Show |
16 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.233+2077G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035938 | |||||||
chr5:136035991 | C | T | 1 | a0001c0004t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.233+2130C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136035991 | |||||||
chr5:136036068 | G | T | 1 | a0001c0004t0003g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+2207G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136036068 | |||||||
chr5:136036074 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.233+2213G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136036074 | |||||||
chr5:136036102 | T | A | 1 | a0001c0003t0002g0074 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.233+2241T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136036102 | |||||||
chr5:136036316 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+2455A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136036316 | |||||||
chr5:136036535 | T | C | 1 | a0001c0003t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.233+2674T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136036535 | |||||||
chr5:136036841 | A | C | 1 | a0001c0007t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.233+2980A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136036841 | |||||||
chr5:136037162 | C | G | 1 | a0001c0003t0001g0038 | 2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.233+3301C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037162 | |||||||
chr5:136037259 | G | A | 1 | a0001c0003t0001g0068 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.233+3398G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037259 | |||||||
chr5:136037444 | G | A | 1 | a0001c0003t0001g0031 | 2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.233+3583G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037444 | |||||||
chr5:136037595 | A | G | 1 | a0001c0004t0003g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+3734A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037595 | |||||||
chr5:136037760 | C | A | 1 | a0001c0004t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.233+3899C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037760 | |||||||
chr5:136037800 | A | G | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233+3939A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037800 | |||||||
chr5:136037917 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.233+4056G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037917 | |||||||
chr5:136037952 | A | G | 1 | a0001c0003t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.233+4091A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136037952 | |||||||
chr5:136038119 | C | G | 1 | a0001c0001t0002g0188 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.233+4258C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038119 | |||||||
chr5:136038173 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0003g0169 a0001c0004t0003g0009 others(2): Show |
10 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+4312G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038173 | |||||||
chr5:136038255 | G | A | 4 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(1): Show |
6 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+4394G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038255 | |||||||
chr5:136038487 | C | T | 1 | a0001c0004t0003g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+4626C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038487 | |||||||
chr5:136038512 | G | C | 182 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(179): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.233+4651G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038512 | |||||||
chr5:136038512 | G | T | 12 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(9): Show |
15 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.233+4651G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038512 | |||||||
chr5:136038546 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG02717.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.233+4685C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038546 | |||||||
chr5:136038626 | C | T | 54 | a0001c0001t0002g0163 a0001c0003t0001g0005 a0001c0003t0001g0010 others(51): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.233+4765C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038626 | |||||||
chr5:136038629 | G | A | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.233+4768G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038629 | |||||||
chr5:136038644 | C | G | 1 | a0006c0015t0001g0175 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.233+4783C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038644 | |||||||
chr5:136038720 | C | CA | 43 | a0001c0001t0001g0099 a0001c0001t0002g0163 a0001c0001t0003g0169 others(40): Show |
80 | HG00673.hp1 HG01884.hp1 HG01891.hp1 others(77): Show |
intron_variant | MODIFIER | c.233+4872dupA | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 136038720 | ||||||
chr5:136038720 | C | CAA | 84 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(81): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.233+4871_233+4872d others(4): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 136038720 | ||||||
chr5:136038848 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.233+4987G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038848 | |||||||
chr5:136038982 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.234-5076A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136038982 | |||||||
chr5:136039057 | A | T | 1 | a0001c0005t0004g0058 | 2 | NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.234-5001A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039057 | |||||||
chr5:136039153 | A | G | 2 | a0001c0002t0001g0033 a0001c0002t0001g0097 |
3 | HG01261.hp1 HG02148.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.234-4905A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039153 | |||||||
chr5:136039353 | T | C | 132 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(129): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.234-4705T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039353 | |||||||
chr5:136039368 | G | T | 1 | a0001c0001t0002g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.234-4690G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039368 | |||||||
chr5:136039477 | G | A | 1 | a0001c0007t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234-4581G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039477 | |||||||
chr5:136039595 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.234-4463G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039595 | |||||||
chr5:136039642 | C | T | 47 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0015 others(44): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.234-4416C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039642 | |||||||
chr5:136039784 | A | G | 129 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(126): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.234-4274A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039784 | |||||||
chr5:136039795 | G | A | 1 | a0001c0004t0003g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.234-4263G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039795 | |||||||
chr5:136039908 | G | A | 54 | a0001c0001t0002g0163 a0001c0003t0001g0005 a0001c0003t0001g0010 others(51): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-4150G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039908 | |||||||
chr5:136039916 | G | A | 56 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(53): Show |
116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.234-4142G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136039916 | |||||||
chr5:136040081 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.234-3977C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136040081 | |||||||
chr5:136040160 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.234-3898C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136040160 | |||||||
chr5:136040295 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.234-3763A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136040295 | |||||||
chr5:136040461 | G | C | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.234-3597G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136040461 | |||||||
chr5:136040907 | C | T | 1 | a0001c0004t0001g0087 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234-3151C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136040907 | |||||||
chr5:136041161 | G | A | 1 | a0001c0004t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234-2897G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041161 | |||||||
chr5:136041267 | T | C | 1 | a0001c0005t0004g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-2791T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041267 | |||||||
chr5:136041321 | C | G | 1 | a0001c0003t0002g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.234-2737C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041321 | |||||||
chr5:136041410 | A | G | 1 | a0001c0002t0001g0111 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.234-2648A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041410 | |||||||
chr5:136041520 | C | T | 1 | a0001c0007t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.234-2538C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041520 | |||||||
chr5:136041660 | C | A | 122 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(119): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.234-2398C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041660 | |||||||
chr5:136041815 | T | A | 1 | a0001c0001t0002g0022 | 3 | NA18951.hp1 NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.234-2243T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041815 | |||||||
chr5:136041877 | C | T | 123 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(120): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.234-2181C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041877 | |||||||
chr5:136041973 | C | T | 7 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(4): Show |
10 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2085C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136041973 | |||||||
chr5:136042041 | T | G | 114 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(111): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.234-2017T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042041 | |||||||
chr5:136042113 | A | C | 129 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(126): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.234-1945A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042113 | |||||||
chr5:136042404 | T | A | 3 | a0001c0004t0003g0045 a0001c0007t0001g0121 a0001c0021t0003g0045 |
3 | HG02970.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.234-1654T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042404 | |||||||
chr5:136042439 | G | A | 4 | a0001c0003t0001g0016 a0001c0003t0001g0029 a0001c0003t0001g0077 others(1): Show |
7 | NA18947.hp2 NA18949.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-1619G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042439 | |||||||
chr5:136042550 | G | C | 167 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(164): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.234-1508G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042550 | |||||||
chr5:136042554 | C | A | 1 | a0001c0007t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234-1504C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042554 | |||||||
chr5:136042657 | G | A | 4 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0170 others(1): Show |
9 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.234-1401G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042657 | |||||||
chr5:136042674 | G | GA | 64 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(61): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.234-1375dupA | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 136042674 | ||||||
chr5:136042758 | T | C | 3 | a0001c0004t0003g0045 a0001c0007t0001g0121 a0001c0021t0003g0045 |
3 | HG02970.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.234-1300T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042758 | |||||||
chr5:136042896 | A | G | 14 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0048 others(11): Show |
26 | HG00423.hp1 HG00438.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.234-1162A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042896 | |||||||
chr5:136042954 | G | A | 1 | a0007c0014t0002g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.234-1104G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136042954 | |||||||
chr5:136043092 | A | G | 95 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(92): Show |
175 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.234-966A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043092 | |||||||
chr5:136043142 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234-916G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043142 | |||||||
chr5:136043423 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0100 |
5 | HG01243.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-635C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043423 | |||||||
chr5:136043525 | C | T | 1 | a0001c0007t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.234-533C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043525 | |||||||
chr5:136043652 | A | C | 195 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(192): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.234-406A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043652 | |||||||
chr5:136043701 | C | T | 1 | a0001c0003t0001g0036 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.234-357C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043701 | |||||||
chr5:136043760 | G | C | 1 | a0001c0004t0003g0055 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234-298G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043760 | |||||||
chr5:136043807 | T | G | 8 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(5): Show |
15 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.234-251T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043807 | |||||||
chr5:136043923 | A | G | 195 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(192): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.234-135A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043923 | |||||||
chr5:136043982 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234-76T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 2/16 | chr5 | 136043982 | |||||||
chr5:136044216 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.298+94G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044216 | |||||||
chr5:136044277 | C | T | 1 | a0001c0003t0001g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.298+155C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044277 | |||||||
chr5:136044334 | C | A | 1 | a0001c0003t0002g0089 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.298+212C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044334 | |||||||
chr5:136044370 | G | A | 86 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(83): Show |
159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.298+248G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044370 | |||||||
chr5:136044379 | A | G | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.298+257A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044379 | |||||||
chr5:136044603 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.298+481G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044603 | |||||||
chr5:136044676 | G | A | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+554G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044676 | |||||||
chr5:136044692 | C | A | 1 | a0001c0003t0001g0038 | 2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.298+570C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136044692 | |||||||
chr5:136045061 | A | C | 1 | a0001c0003t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.298+939A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045061 | |||||||
chr5:136045075 | C | T | 91 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(88): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.298+953C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045075 | |||||||
chr5:136045217 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298+1095C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045217 | |||||||
chr5:136045505 | G | A | 1 | a0001c0007t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-830G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045505 | |||||||
chr5:136045547 | A | AAAAT | 3 | a0001c0003t0001g0080 a0001c0003t0002g0090 a0001c0004t0001g0191 |
3 | HG02280.hp2 HG02523.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.299-763_299-760dup others(4): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 136045547 | ||||||
chr5:136045602 | A | T | 12 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(9): Show |
18 | HG01069.hp1 HG01243.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-733A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045602 | |||||||
chr5:136045657 | C | T | 8 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(5): Show |
15 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-678C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045657 | |||||||
chr5:136045805 | G | C | 8 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(5): Show |
15 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-530G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045805 | |||||||
chr5:136045850 | G | T | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-485G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045850 | |||||||
chr5:136045992 | A | T | 5 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-343A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136045992 | |||||||
chr5:136046128 | C | T | 1 | a0001c0004t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.299-207C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136046128 | |||||||
chr5:136046149 | T | C | 1 | a0001c0001t0002g0048 | 2 | HG01099.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.299-186T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136046149 | |||||||
chr5:136046221 | T | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0128 |
3 | HG01099.hp2 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.299-114T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 3/16 | chr5 | 136046221 | |||||||
chr5:136046540 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.459+45C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 4/16 | chr5 | 136046540 | |||||||
chr5:136046552 | G | A | 23 | a0001c0004t0001g0191 a0001c0004t0003g0045 a0001c0005t0002g0025 others(20): Show |
35 | HG00741.hp1 HG02083.hp1 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.459+57G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 4/16 | chr5 | 136046552 | |||||||
chr5:136046692 | A | T | 1 | a0001c0002t0001g0110 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.460-159A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 4/16 | chr5 | 136046692 | |||||||
chr5:136046757 | C | T | 1 | a0001c0004t0001g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460-94C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 4/16 | chr5 | 136046757 | |||||||
chr5:136046834 | C | T | 14 | a0001c0001t0003g0169 a0001c0004t0001g0191 a0001c0004t0003g0009 others(11): Show |
27 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.460-17C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 4/16 | chr5 | 136046834 | |||||||
chr5:136046835 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0148 |
4 | HG01109.hp1 HG01175.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-16C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 4/16 | chr5 | 136046835 | |||||||
chr5:136047118 | C | A | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.624+103C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 5/16 | chr5 | 136047118 | |||||||
chr5:136047155 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.625-119C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 5/16 | chr5 | 136047155 | |||||||
chr5:136047539 | A | G | 61 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(58): Show |
121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.771+119A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136047539 | |||||||
chr5:136047668 | G | A | 50 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0015 others(47): Show |
95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.771+248G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136047668 | |||||||
chr5:136047688 | T | G | 94 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(91): Show |
174 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.771+268T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136047688 | |||||||
chr5:136047741 | A | G | 84 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(81): Show |
163 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.771+321A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136047741 | |||||||
chr5:136047926 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.771+506G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136047926 | |||||||
chr5:136048146 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.771+726G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048146 | |||||||
chr5:136048204 | T | C | 94 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(91): Show |
174 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.771+784T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048204 | |||||||
chr5:136048255 | C | T | 3 | a0001c0005t0004g0014 a0001c0005t0004g0057 a0001c0005t0004g0173 |
7 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+835C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048255 | |||||||
chr5:136048392 | G | A | 75 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(72): Show |
147 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.771+972G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048392 | |||||||
chr5:136048403 | C | T | 8 | a0001c0003t0001g0010 a0001c0003t0001g0015 a0001c0003t0001g0030 others(5): Show |
15 | HG00597.hp2 HG00621.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.771+983C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048403 | |||||||
chr5:136048439 | C | T | 5 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-1000C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048439 | |||||||
chr5:136048531 | C | A | 5 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0047 others(2): Show |
11 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.772-908C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048531 | |||||||
chr5:136048617 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.772-822T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048617 | |||||||
chr5:136048647 | G | A | 9 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(6): Show |
16 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.772-792G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048647 | |||||||
chr5:136048687 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.772-752C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048687 | |||||||
chr5:136048754 | A | G | 50 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0021 others(47): Show |
127 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.772-685A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048754 | |||||||
chr5:136048980 | C | T | 10 | a0001c0004t0003g0045 a0001c0007t0001g0121 a0001c0007t0001g0122 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-459C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048980 | |||||||
chr5:136048991 | G | A | 196 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(193): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.772-448G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136048991 | |||||||
chr5:136049118 | A | G | 1 | a0001c0007t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.772-321A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049118 | |||||||
chr5:136049141 | A | G | 4 | a0001c0004t0001g0034 a0001c0004t0001g0078 a0001c0004t0001g0079 others(1): Show |
5 | HG00735.hp2 HG01433.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-298A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049141 | |||||||
chr5:136049156 | T | A | 95 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(92): Show |
175 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.772-283T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049156 | |||||||
chr5:136049235 | A | G | 5 | a0001c0004t0003g0024 a0001c0004t0003g0055 a0001c0004t0003g0066 others(2): Show |
8 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-204A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049235 | |||||||
chr5:136049280 | G | A | 5 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0047 others(2): Show |
11 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.772-159G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049280 | |||||||
chr5:136049343 | C | G | 1 | a0001c0001t0002g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.772-96C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049343 | |||||||
chr5:136049343 | C | T | 4 | a0001c0007t0002g0053 a0001c0007t0002g0162 a0001c0017t0001g0164 others(1): Show |
5 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-96C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049343 | |||||||
chr5:136049413 | C | G | 1 | a0001c0001t0002g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.772-26C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 6/16 | chr5 | 136049413 | |||||||
chr5:136049627 | T | C | 95 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(92): Show |
175 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.913+47T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136049627 | |||||||
chr5:136049667 | C | T | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.913+87C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136049667 | |||||||
chr5:136049937 | G | A | 4 | a0001c0005t0004g0014 a0001c0005t0004g0057 a0001c0005t0004g0058 others(1): Show |
9 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.913+357G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136049937 | |||||||
chr5:136049981 | G | C | 1 | a0001c0001t0003g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.913+401G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136049981 | |||||||
chr5:136050011 | T | C | 95 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(92): Show |
175 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.913+431T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050011 | |||||||
chr5:136050089 | T | C | 85 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(82): Show |
164 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.913+509T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050089 | |||||||
chr5:136050196 | G | A | 1 | a0001c0003t0002g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.913+616G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050196 | |||||||
chr5:136050215 | C | T | 2 | a0001c0004t0001g0191 a0002c0008t0001g0012 |
5 | HG01891.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+635C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050215 | |||||||
chr5:136050327 | G | A | 2 | a0001c0002t0001g0044 a0001c0002t0001g0119 |
3 | HG00639.hp2 HG01109.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.913+747G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050327 | |||||||
chr5:136050334 | GA | G | 119 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(116): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.913+771delA | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 136050334 | ||||||
chr5:136050334 | GAA | G | 15 | a0001c0001t0002g0147 a0001c0002t0001g0109 a0001c0003t0001g0189 others(12): Show |
23 | HG00558.hp1 HG02083.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.913+770_913+771del others(2): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 136050334 | ||||||
chr5:136050470 | C | T | 1 | a0001c0018t0004g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.913+890C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050470 | |||||||
chr5:136050570 | A | G | 9 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(6): Show |
16 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.913+990A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050570 | |||||||
chr5:136050693 | C | A | 2 | a0001c0003t0001g0017 a0001c0003t0001g0086 |
4 | HG00642.hp2 HG01106.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.913+1113C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050693 | |||||||
chr5:136050712 | T | C | 2 | a0001c0001t0002g0063 a0004c0020t0002g0136 |
2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.913+1132T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050712 | |||||||
chr5:136050839 | G | A | 1 | a0001c0003t0002g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.913+1259G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050839 | |||||||
chr5:136050910 | G | A | 4 | a0001c0003t0001g0015 a0001c0003t0001g0030 a0001c0003t0001g0067 others(1): Show |
7 | HG00597.hp2 HG00621.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+1330G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050910 | |||||||
chr5:136050941 | C | T | 2 | a0001c0001t0002g0127 a0001c0001t0002g0130 |
2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.913+1361C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136050941 | |||||||
chr5:136051041 | A | G | 80 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(77): Show |
153 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.913+1461A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051041 | |||||||
chr5:136051064 | G | T | 76 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(73): Show |
148 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.913+1484G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051064 | |||||||
chr5:136051110 | G | T | 1 | a0001c0001t0002g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.913+1530G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051110 | |||||||
chr5:136051111 | C | T | 76 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(73): Show |
148 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.913+1531C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051111 | |||||||
chr5:136051183 | A | T | 1 | a0001c0004t0003g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913+1603A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051183 | |||||||
chr5:136051200 | C | T | 8 | a0001c0007t0001g0121 a0001c0007t0001g0122 a0001c0007t0001g0123 others(5): Show |
9 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.913+1620C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051200 | |||||||
chr5:136051510 | G | A | 5 | a0001c0004t0001g0152 a0001c0004t0002g0051 a0001c0004t0002g0151 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-1397G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051510 | |||||||
chr5:136051553 | G | T | 1 | a0001c0003t0002g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.914-1354G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051553 | |||||||
chr5:136051800 | A | G | 6 | a0001c0007t0001g0121 a0001c0007t0001g0123 a0001c0007t0002g0053 others(3): Show |
7 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-1107A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051800 | |||||||
chr5:136051892 | C | A | 1 | a0001c0002t0001g0184 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.914-1015C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051892 | |||||||
chr5:136051989 | G | A | 8 | a0001c0007t0001g0121 a0001c0007t0001g0122 a0001c0007t0001g0123 others(5): Show |
9 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.914-918G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136051989 | |||||||
chr5:136052077 | G | A | 2 | a0001c0003t0001g0091 a0001c0003t0001g0094 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.914-830G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052077 | |||||||
chr5:136052114 | A | G | 92 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(89): Show |
174 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.914-793A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052114 | |||||||
chr5:136052168 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.914-739G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052168 | |||||||
chr5:136052170 | C | G | 1 | a0001c0007t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.914-737C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052170 | |||||||
chr5:136052222 | G | A | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-685G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052222 | |||||||
chr5:136052384 | C | T | 8 | a0001c0007t0001g0121 a0001c0007t0001g0122 a0001c0007t0001g0123 others(5): Show |
9 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.914-523C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052384 | |||||||
chr5:136052408 | TTCGTCTT others(10): Show |
T | 1 | a0001c0001t0002g0145 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.914-498_914-482del others(17): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052408 | |||||||
chr5:136052464 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.914-443C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052464 | |||||||
chr5:136052479 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.914-428C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052479 | |||||||
chr5:136052566 | G | A | 1 | a0001c0001t0002g0050 | 2 | HG02135.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.914-341G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052566 | |||||||
chr5:136052584 | T | A | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.914-323T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052584 | |||||||
chr5:136052878 | G | A | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-29G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052878 | |||||||
chr5:136052900 | A | C | 1 | a0001c0002t0001g0186 | 1 | HG00558.hp2 | splice_region_variant&intron_variant | LOW | c.914-7A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 7/16 | chr5 | 136052900 | |||||||
chr5:136053452 | C | T | 1 | a0001c0003t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1126+333C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 8/16 | chr5 | 136053452 | |||||||
chr5:136053510 | T | A | 22 | a0001c0001t0003g0169 a0001c0004t0001g0191 a0001c0004t0003g0009 others(19): Show |
38 | HG01884.hp1 HG02083.hp1 HG02129.hp2 others(35): Show |
intron_variant | MODIFIER | c.1126+391T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 8/16 | chr5 | 136053510 | |||||||
chr5:136053736 | C | A | 88 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(85): Show |
169 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1127-207C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 8/16 | chr5 | 136053736 | |||||||
chr5:136053744 | C | T | 50 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0021 others(47): Show |
127 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1127-199C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 8/16 | chr5 | 136053744 | |||||||
chr5:136053867 | T | G | 1 | a0001c0003t0001g0082 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1127-76T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 8/16 | chr5 | 136053867 | |||||||
chr5:136054325 | G | A | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1264+245G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 9/16 | chr5 | 136054325 | |||||||
chr5:136054382 | A | G | 1 | a0001c0001t0002g0142 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1264+302A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 9/16 | chr5 | 136054382 | |||||||
chr5:136054553 | A | G | 2 | a0001c0002t0001g0101 a0001c0002t0001g0108 |
2 | HG01123.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1265-163A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 9/16 | chr5 | 136054553 | |||||||
chr5:136054705 | C | T | 1 | a0001c0003t0002g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1265-11C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 9/16 | chr5 | 136054705 | |||||||
chr5:136054950 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1410+89G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136054950 | |||||||
chr5:136054958 | A | C | 1 | a0001c0007t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1410+97A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136054958 | |||||||
chr5:136055036 | G | A | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1410+175G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136055036 | |||||||
chr5:136055199 | T | C | 8 | a0001c0007t0001g0121 a0001c0007t0001g0122 a0001c0007t0001g0123 others(5): Show |
9 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1410+338T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136055199 | |||||||
chr5:136055637 | A | G | 96 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(93): Show |
178 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1411-43A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136055637 | |||||||
chr5:136055659 | C | T | 1 | a0001c0002t0001g0042 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1411-21C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136055659 | |||||||
chr5:136055677 | C | T | 9 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(6): Show |
16 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1411-3C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 10/16 | chr5 | 136055677 | |||||||
chr5:136056021 | A | G | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1547+205A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/16 | chr5 | 136056021 | |||||||
chr5:136056058 | G | A | 1 | a0001c0007t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1547+242G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/16 | chr5 | 136056058 | |||||||
chr5:136056125 | C | A | 1 | a0001c0004t0001g0078 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1547+309C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/16 | chr5 | 136056125 | |||||||
chr5:136056258 | T | C | 100 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(97): Show |
183 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1548-407T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/16 | chr5 | 136056258 | |||||||
chr5:136056413 | T | C | 100 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(97): Show |
183 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1548-252T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/16 | chr5 | 136056413 | |||||||
chr5:136056635 | A | G | 9 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(6): Show |
16 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1548-30A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 11/16 | chr5 | 136056635 | |||||||
chr5:136056818 | G | A | 36 | a0001c0001t0001g0155 a0001c0001t0002g0002 a0001c0001t0002g0007 others(33): Show |
78 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1678+23G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136056818 | |||||||
chr5:136057046 | T | A | 100 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(97): Show |
183 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1678+251T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057046 | |||||||
chr5:136057130 | C | T | 1 | a0001c0002t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1678+335C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057130 | |||||||
chr5:136057328 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1678+533A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057328 | |||||||
chr5:136057449 | C | T | 50 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0021 others(47): Show |
127 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1678+654C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057449 | |||||||
chr5:136057508 | A | G | 100 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(97): Show |
183 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1678+713A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057508 | |||||||
chr5:136057892 | T | A | 1 | a0001c0002t0001g0187 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1678+1097T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057892 | |||||||
chr5:136057934 | C | T | 1 | a0001c0006t0001g0166 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1678+1139C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136057934 | |||||||
chr5:136058065 | T | C | 147 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(144): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1679-1025T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058065 | |||||||
chr5:136058120 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1679-970A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058120 | |||||||
chr5:136058140 | G | C | 1 | a0001c0003t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1679-950G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058140 | |||||||
chr5:136058253 | A | G | 1 | a0001c0005t0004g0173 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1679-837A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058253 | |||||||
chr5:136058382 | G | A | 1 | a0001c0002t0001g0040 | 2 | HG03688.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1679-708G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058382 | |||||||
chr5:136058498 | G | A | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1679-592G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058498 | |||||||
chr5:136058787 | G | C | 6 | a0001c0007t0001g0121 a0001c0007t0001g0123 a0001c0007t0002g0053 others(3): Show |
7 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1679-303G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058787 | |||||||
chr5:136058870 | A | T | 1 | a0001c0005t0004g0057 | 2 | HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1679-220A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 12/16 | chr5 | 136058870 | |||||||
chr5:136059242 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1803+28C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059242 | |||||||
chr5:136059253 | C | G | 10 | a0001c0005t0002g0025 a0001c0005t0002g0172 a0001c0005t0004g0014 others(7): Show |
17 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.1803+39C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059253 | |||||||
chr5:136059483 | T | G | 1 | a0001c0003t0002g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1803+269T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059483 | |||||||
chr5:136059514 | T | C | 147 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(144): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1803+300T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059514 | |||||||
chr5:136059523 | A | T | 1 | a0001c0005t0004g0056 | 2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1803+309A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059523 | |||||||
chr5:136059535 | G | C | 197 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(194): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1803+321G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059535 | |||||||
chr5:136059546 | A | G | 1 | a0001c0002t0001g0149 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1803+332A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059546 | |||||||
chr5:136059701 | A | G | 2 | a0001c0004t0001g0152 a0001c0004t0002g0167 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1803+487A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059701 | |||||||
chr5:136059721 | G | A | 20 | a0001c0001t0002g0006 a0001c0001t0002g0048 a0001c0001t0002g0049 others(17): Show |
41 | HG00423.hp1 HG00438.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1803+507G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059721 | |||||||
chr5:136059744 | A | G | 145 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(142): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1803+530A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059744 | |||||||
chr5:136059773 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1803+559C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059773 | |||||||
chr5:136059854 | G | C | 145 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(142): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1803+640G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059854 | |||||||
chr5:136059913 | T | TA | 7 | a0001c0003t0001g0020 a0001c0003t0001g0091 a0001c0003t0001g0092 others(4): Show |
12 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1803+700dupA | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr5 | 136059913 | ||||||
chr5:136059937 | C | T | 51 | a0001c0001t0003g0169 a0001c0002t0001g0105 a0001c0003t0001g0005 others(48): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1803+723C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059937 | |||||||
chr5:136059967 | C | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0139 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1803+753C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136059967 | |||||||
chr5:136060099 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1804-735G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060099 | |||||||
chr5:136060136 | TC | T | 132 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(129): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1804-696delC | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr5 | 136060136 | ||||||
chr5:136060138 | C | G | 132 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(129): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1804-696C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060138 | |||||||
chr5:136060168 | G | A | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1804-666G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060168 | |||||||
chr5:136060172 | T | G | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1804-662T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060172 | |||||||
chr5:136060175 | G | C | 132 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(129): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1804-659G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060175 | |||||||
chr5:136060395 | A | T | 132 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(129): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1804-439A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060395 | |||||||
chr5:136060404 | C | A | 1 | a0001c0003t0001g0035 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.1804-430C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060404 | |||||||
chr5:136060469 | G | A | 1 | a0001c0002t0001g0097 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1804-365G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060469 | |||||||
chr5:136060526 | C | A | 1 | a0001c0002t0001g0041 | 2 | HG01070.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1804-308C>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060526 | |||||||
chr5:136060538 | A | T | 196 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(193): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1804-296A>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060538 | |||||||
chr5:136060570 | C | T | 1 | a0001c0003t0001g0020 | 3 | HG02647.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1804-264C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060570 | |||||||
chr5:136060593 | A | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-241A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060593 | |||||||
chr5:136060595 | A | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-239A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060595 | |||||||
chr5:136060596 | G | A | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-238G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060596 | |||||||
chr5:136060598 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-236T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060598 | |||||||
chr5:136060603 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-231T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060603 | |||||||
chr5:136060603 | T | G | 131 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(128): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1804-231T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060603 | |||||||
chr5:136060604 | G | A | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-230G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060604 | |||||||
chr5:136060605 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-229G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060605 | |||||||
chr5:136060607 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-227G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060607 | |||||||
chr5:136060608 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-226G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060608 | |||||||
chr5:136060610 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-224T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060610 | |||||||
chr5:136060611 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-223G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060611 | |||||||
chr5:136060613 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-221G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060613 | |||||||
chr5:136060614 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-220G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060614 | |||||||
chr5:136060619 | A | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-215A>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060619 | |||||||
chr5:136060620 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-214G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060620 | |||||||
chr5:136060623 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-211T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060623 | |||||||
chr5:136060654 | G | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-180G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060654 | |||||||
chr5:136060656 | G | T | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1804-178G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060656 | |||||||
chr5:136060736 | G | A | 4 | a0001c0006t0001g0011 a0001c0006t0001g0165 a0001c0006t0001g0166 others(1): Show |
8 | HG02155.hp2 NA18940.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1804-98G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060736 | |||||||
chr5:136060763 | A | G | 134 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(131): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1804-71A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060763 | |||||||
chr5:136060779 | T | A | 134 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(131): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1804-55T>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060779 | |||||||
chr5:136060799 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0100 |
5 | HG01243.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1804-35C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060799 | |||||||
chr5:136060826 | T | TCCCCCCC others(16): Show |
1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.1804-7_1804-6insCC others(21): Show |
TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr5 | 136060826 | ||||||
chr5:136060828 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.1804-6T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060828 | |||||||
chr5:136060829 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.1804-5T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060829 | |||||||
chr5:136060831 | T | C | 1 | a0005c0016t0002g0098 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.1804-3T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 13/16 | chr5 | 136060831 | |||||||
chr5:136060980 | T | C | 134 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(131): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1906+44T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136060980 | |||||||
chr5:136061058 | G | C | 4 | a0001c0007t0002g0053 a0001c0007t0002g0162 a0001c0017t0001g0164 others(1): Show |
5 | HG00741.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+122G>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061058 | |||||||
chr5:136061108 | G | A | 1 | a0001c0007t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906+172G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061108 | |||||||
chr5:136061109 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1906+173C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061109 | |||||||
chr5:136061146 | C | T | 1 | a0001c0003t0002g0018 | 3 | HG03471.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1906+210C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061146 | |||||||
chr5:136061171 | C | G | 1 | a0001c0003t0001g0077 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1906+235C>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061171 | |||||||
chr5:136061200 | C | T | 1 | a0001c0003t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1906+264C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061200 | |||||||
chr5:136061216 | G | A | 1 | a0001c0002t0001g0184 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1906+280G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061216 | |||||||
chr5:136061218 | G | A | 1 | a0001c0003t0001g0036 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1906+282G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061218 | |||||||
chr5:136061240 | C | T | 3 | a0001c0001t0001g0155 a0001c0002t0001g0044 a0001c0002t0001g0119 |
4 | HG00639.hp2 HG01109.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-260C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061240 | |||||||
chr5:136061329 | T | C | 147 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(144): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1907-171T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061329 | |||||||
chr5:136061419 | A | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0137 |
10 | HG02027.hp2 NA18951.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.1907-81A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 14/16 | chr5 | 136061419 | |||||||
chr5:136061699 | T | G | 1 | a0001c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1986+120T>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136061699 | |||||||
chr5:136061807 | C | T | 1 | a0001c0002t0001g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1986+228C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136061807 | |||||||
chr5:136061994 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1986+415G>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136061994 | |||||||
chr5:136062013 | T | C | 100 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(97): Show |
197 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.1986+434T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136062013 | |||||||
chr5:136062041 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0178 |
7 | HG01243.hp2 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1986+462C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136062041 | |||||||
chr5:136062096 | C | T | 87 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(84): Show |
174 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1986+517C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136062096 | |||||||
chr5:136062272 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1987-391G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136062272 | |||||||
chr5:136062285 | T | C | 196 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0158 others(193): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1987-378T>C | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136062285 | |||||||
chr5:136062590 | G | A | 39 | a0001c0001t0001g0099 a0001c0001t0001g0158 a0001c0001t0001g0159 others(36): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.1987-73G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 15/16 | chr5 | 136062590 | |||||||
chr5:136062739 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2011+52C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136062739 | |||||||
chr5:136062771 | A | G | 2 | a0001c0004t0002g0051 a0001c0004t0002g0151 |
3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2011+84A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136062771 | |||||||
chr5:136062824 | C | T | 9 | a0001c0003t0002g0004 a0001c0003t0002g0037 a0001c0003t0002g0071 others(6): Show |
19 | HG00673.hp1 HG02523.hp1 NA18747.hp1 others(16): Show |
intron_variant | MODIFIER | c.2011+137C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136062824 | |||||||
chr5:136062856 | C | T | 13 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0024 others(10): Show |
23 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2011+169C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136062856 | |||||||
chr5:136062934 | G | A | 1 | a0001c0003t0001g0083 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2011+247G>A | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136062934 | |||||||
chr5:136063000 | A | G | 13 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0024 others(10): Show |
23 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2012-186A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136063000 | |||||||
chr5:136063001 | C | T | 1 | a0001c0003t0001g0068 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2012-185C>T | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136063001 | |||||||
chr5:136063002 | A | G | 13 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0024 others(10): Show |
23 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2012-184A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136063002 | |||||||
chr5:136063139 | A | G | 13 | a0001c0001t0003g0169 a0001c0004t0003g0009 a0001c0004t0003g0024 others(10): Show |
23 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2012-47A>G | TGFBI | ENSG00000120708.17 | transcript | ENST00000442011.7 | protein_coding | 16/16 | chr5 | 136063139 |