Item | Value |
---|---|
geneid | 7043 |
ensemblid | ENSG00000119699.8 |
hgncid | 11769 |
symbol | TGFB3 |
name | transforming growth factor beta 3 |
refseq_nuc | NM_003239.5 |
refseq_prot | NP_003230.1 |
ensembl_nuc | ENST00000238682.8 |
ensembl_prot | ENSP00000238682.3 |
mane_status | MANE Select |
chr | chr14 |
start | 75958097 |
end | 75981995 |
strand | - |
ver | v1.2 |
region | chr14:75958097-75981995 |
region5000 | chr14:75953097-75986995 |
regionname0 | TGFB3_chr14_75958097_75981995 |
regionname5000 | TGFB3_chr14_75953097_75986995 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 412 | 377 | 94 | 72 | 165 | 8 | 36 | 128 | TGFB3_chr14_75953097_75986995 | TGFB3 | MKMHL others(407): Show |
chr14 | 75953097 | 75986995 |
a0002 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | MKMHL others(407): Show |
chr14 | 75953097 | 75986995 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1236 | 363 | 87 | 72 | 158 | 8 | 36 | TGFB3_chr14_75953097_75986995 | TGFB3 | ATGAA others(1231): Show |
chr14 | 75953097 | 75986995 | ||
a0001c0002 | 0/0 | 1236 | 6 | 0 | 0 | 6 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | ATGAA others(1231): Show |
chr14 | 75953097 | 75986995 | ||
a0001c0003 | 0/0 | 1236 | 5 | 5 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | ATGAA others(1231): Show |
chr14 | 75953097 | 75986995 | ||
a0001c0004 | 0/0 | 1236 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | ATGAA others(1231): Show |
chr14 | 75953097 | 75986995 | ||
a0001c0005 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | ATGAA others(1231): Show |
chr14 | 75953097 | 75986995 | ||
a0002c0006 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | ATGAA others(1231): Show |
chr14 | 75953097 | 75986995 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3431 | 300 | 64 | 55 | 144 | 7 | 28 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0002 | 0/0 | 3431 | 10 | 1 | 5 | 0 | 0 | 4 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0003 | 0/0 | 3425 | 9 | 0 | 8 | 0 | 1 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3420): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0004 | 0/0 | 3431 | 8 | 8 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0005 | 0/0 | 3430 | 7 | 1 | 1 | 5 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3425): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0006 | 0/0 | 3431 | 6 | 0 | 0 | 6 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0007 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0008 | 0/0 | 3431 | 3 | 1 | 0 | 0 | 0 | 2 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0009 | 0/0 | 3432 | 3 | 2 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3427): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0010 | 0/0 | 3432 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3427): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0011 | 0/0 | 3431 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0012 | 0/0 | 3431 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0013 | 0/0 | 3424 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3419): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0015 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0016 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0017 | 0/0 | 3430 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3425): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0018 | 0/0 | 3431 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0019 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0020 | 0/0 | 3432 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3427): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0021 | 0/0 | 3431 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0022 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3425): Show |
chr14 | 75953097 | 75986995 |
a0001c0001t0023 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0002t0001 | 0/0 | 3431 | 6 | 0 | 0 | 6 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0003t0007 | 0/0 | 3431 | 4 | 4 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0003t0014 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0004t0001 | 0/0 | 3431 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0001c0005t0001 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
a0002c0006t0001 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | AGCAG others(3426): Show |
chr14 | 75953097 | 75986995 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 1 | 10 | 11 | 1 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0002 | 1/0 | 14 | 0 | 1 | 11 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 4 | 4 | 1 | 2 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0004 | 0/0 | 8 | 1 | 1 | 4 | 1 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0010 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0012 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0022 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0060 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0061 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0004g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0006g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0012g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0013g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0015g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0018g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0019g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0020g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0022g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0001t0023g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0003t0007g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0003t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0003t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0003t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0001c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
a0002c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | GBR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00438 | hp1 | a0001 | c0005 | t0001 | g0223 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00609 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01168 | hp1 | a0001 | c0001 | t0013 | g0063 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0075 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01261 | hp1 | a0001 | c0001 | t0018 | g0126 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01891 | hp1 | a0001 | c0003 | t0007 | g0058 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02055 | hp1 | a0001 | c0003 | t0014 | g0067 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02132 | hp1 | a0001 | c0001 | t0023 | g0227 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02165 | hp1 | a0002 | c0006 | t0001 | g0224 | EAS | CDX | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0071 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0095 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02273 | hp2 | a0001 | c0001 | t0009 | g0123 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02280 | hp2 | a0001 | c0003 | t0007 | g0175 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0199 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0073 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0094 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0226 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0211 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0225 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03239 | hp2 | a0001 | c0001 | t0008 | g0069 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03453 | hp1 | a0001 | c0003 | t0007 | g0109 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03540 | hp2 | a0001 | c0001 | t0019 | g0106 | AFR | GWD | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03654 | hp2 | a0001 | c0001 | t0021 | g0099 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04199 | hp1 | a0001 | c0001 | t0020 | g0108 | SAS | STU | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | STU | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18612 | hp2 | a0001 | c0001 | t0015 | g0068 | EAS | CHB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | CHB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | YRI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18906 | hp2 | a0001 | c0003 | t0007 | g0058 | AFR | YRI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18960 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18963 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18984 | hp2 | a0001 | c0001 | t0022 | g0124 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19012 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0098 | AFR | LWK | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19062 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ASW | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | GIH | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0070 | SAS | GIH | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | USA | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0110 | AFR | LWK | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
NA21309 | hp2 | a0001 | c0001 | t0017 | g0150 | AFR | LWK | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0195 | REF | REF | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | TGFB3_chr14_75953097_75986995 | TGFB3 | chr14 | 75953097 | 75986995 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:75980793 | T | C | 1 | a0002 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.101A>G | p.His34Arg | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 1203/3431 | 101/1239 | 34/412 | chr14 | 75980793 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:75959304 | G | C | 1 | a0001c0003 | 5 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(2): Show |
synonymous_variant | LOW | c.1122C>G | p.Ala374Ala | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 2224/3431 | 1122/1239 | 374/412 | chr14 | 75959304 | |||
chr14:75980606 | G | A | 1 | a0001c0005 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.288C>T | p.Thr96Thr | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 1390/3431 | 288/1239 | 96/412 | chr14 | 75980606 | |||
chr14:75980806 | A | G | 1 | a0001c0002 | 6 | NA18954.hp1 NA18962.hp1 NA18963.hp1 others(3): Show |
synonymous_variant | LOW | c.88T>C | p.Leu30Leu | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 1190/3431 | 88/1239 | 30/412 | chr14 | 75980806 | |||
chr14:75980855 | G | A | 1 | a0001c0004 | 2 | HG02886.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.39C>T | p.Ala13Ala | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 1141/3431 | 39/1239 | 13/412 | chr14 | 75980855 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:75958238 | C | T | 1 | a0001c0001t0018 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 949 | chr14 | 75958238 | ||||||
chr14:75958363 | A | G | 3 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0020 |
3 | HG03540.hp2 HG04199.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*824T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 824 | chr14 | 75958363 | ||||||
chr14:75958367 | C | T | 1 | a0001c0001t0004 | 8 | HG01891.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*820G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 820 | chr14 | 75958367 | ||||||
chr14:75958491 | A | G | 3 | a0001c0001t0007 a0001c0003t0007 a0001c0003t0014 |
6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*696T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 696 | chr14 | 75958491 | ||||||
chr14:75958505 | C | T | 1 | a0001c0001t0011 | 2 | HG02451.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 682 | chr14 | 75958505 | ||||||
chr14:75958521 | T | C | 6 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0019 others(3): Show |
9 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*666A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 666 | chr14 | 75958521 | ||||||
chr14:75958691 | C | T | 1 | a0001c0001t0006 | 6 | HG00609.hp1 NA18960.hp2 NA18963.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*496G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 496 | chr14 | 75958691 | ||||||
chr14:75958704 | T | TA | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0020 |
6 | HG01884.hp1 HG02273.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*482dupT | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 482 | chr14 | 75958704 | ||||||
chr14:75958704 | TA | T | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(1): Show |
10 | HG00609.hp2 HG01168.hp1 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*482delT | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 482 | chr14 | 75958704 | ||||||
chr14:75958932 | G | A | 1 | a0001c0001t0012 | 2 | HG02258.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*255C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 255 | chr14 | 75958932 | ||||||
chr14:75959001 | C | T | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 186 | chr14 | 75959001 | ||||||
chr14:75959002 | G | A | 1 | a0001c0001t0021 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 185 | chr14 | 75959002 | ||||||
chr14:75959178 | C | T | 1 | a0001c0001t0010 | 2 | HG02622.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 9 | chr14 | 75959178 | ||||||
chr14:75959179 | G | A | 1 | a0001c0001t0022 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 7/7 | 8 | chr14 | 75959179 | ||||||
chr14:75981178 | G | A | 1 | a0001c0001t0023 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-285C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 285 | chr14 | 75981178 | ||||||
chr14:75981436 | A | T | 1 | a0001c0001t0008 | 3 | HG02257.hp2 HG03239.hp2 NA20905.hp2 |
5_prime_UTR_variant | MODIFIER | c.-543T>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 543 | chr14 | 75981436 | ||||||
chr14:75981507 | G | A | 1 | a0001c0001t0002 | 10 | HG01106.hp2 HG01928.hp2 HG01981.hp1 others(7): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-614C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | chr14 | 75981507 | |||||||
chr14:75981681 | A | G | 1 | a0001c0001t0015 | 1 | NA18612.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-788T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | chr14 | 75981681 | |||||||
chr14:75981922 | C | T | 1 | a0001c0003t0014 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1029G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 1029 | chr14 | 75981922 | ||||||
chr14:75981923 | TCTCTCC | T | 2 | a0001c0001t0003 a0001c0001t0013 |
10 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-1036_-1031delGGAG others(2): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/7 | 1031 | chr14 | 75981923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:75959491 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1081-146G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959491 | |||||||
chr14:75959516 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1081-171A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959516 | |||||||
chr14:75959643 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0213 others(1): Show |
5 | NA18946.hp1 NA18969.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081-298G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959643 | |||||||
chr14:75959666 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1081-321C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959666 | |||||||
chr14:75959740 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1081-395G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959740 | |||||||
chr14:75959777 | GA | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0161 others(3): Show |
10 | HG01074.hp2 HG01243.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1081-433delT | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959777 | |||||||
chr14:75959791 | C | A | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1081-446G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959791 | |||||||
chr14:75959821 | G | T | 2 | a0001c0001t0010g0073 a0001c0001t0010g0199 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1081-476C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959821 | |||||||
chr14:75959828 | A | G | 2 | a0001c0001t0010g0073 a0001c0001t0010g0199 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1081-483T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959828 | |||||||
chr14:75959845 | A | G | 1 | a0001c0001t0008g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1081-500T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959845 | |||||||
chr14:75959931 | C | CT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
159 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1081-587dupA | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959931 | |||||||
chr14:75959931 | C | CTT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(66): Show |
102 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.1081-588_1081-587d others(4): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959931 | |||||||
chr14:75959931 | C | CTTT | 14 | a0001c0001t0001g0057 a0001c0001t0001g0077 a0001c0001t0001g0087 others(11): Show |
17 | HG00733.hp1 HG01106.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1081-589_1081-587d others(5): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959931 | |||||||
chr14:75959931 | CTT | C | 6 | a0001c0001t0007g0098 a0001c0001t0010g0073 a0001c0001t0010g0199 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081-588_1081-587d others(4): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959931 | |||||||
chr14:75959931 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0148 a0001c0001t0005g0147 |
2 | NA18747.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1081-601_1081-587d others(17): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75959931 | |||||||
chr14:75960237 | C | T | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1080+686G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75960237 | |||||||
chr14:75960359 | G | C | 3 | a0001c0001t0017g0150 a0001c0001t0019g0106 a0001c0001t0020g0108 |
3 | HG03540.hp2 HG04199.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1080+564C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75960359 | |||||||
chr14:75960380 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1080+543G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75960380 | |||||||
chr14:75960676 | C | T | 1 | a0001c0003t0007g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1080+247G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75960676 | |||||||
chr14:75960712 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1080+211G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75960712 | |||||||
chr14:75960760 | A | G | 3 | a0001c0001t0017g0150 a0001c0001t0019g0106 a0001c0001t0020g0108 |
3 | HG03540.hp2 HG04199.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1080+163T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 6/6 | chr14 | 75960760 | |||||||
chr14:75961345 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.927-269G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75961345 | |||||||
chr14:75961437 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.927-361A>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75961437 | |||||||
chr14:75961722 | A | G | 1 | a0001c0001t0004g0050 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.927-646T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75961722 | |||||||
chr14:75961796 | C | A | 10 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0180 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.927-720G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75961796 | |||||||
chr14:75962028 | C | T | 2 | a0001c0001t0017g0150 a0001c0001t0019g0106 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.927-952G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962028 | |||||||
chr14:75962111 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.927-1035G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962111 | |||||||
chr14:75962288 | G | A | 1 | a0001c0001t0020g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.926+1028C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962288 | |||||||
chr14:75962439 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0017g0150 a0001c0001t0019g0106 |
3 | HG03540.hp2 HG03927.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.926+877T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962439 | |||||||
chr14:75962469 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.926+847G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962469 | |||||||
chr14:75962539 | C | T | 1 | a0001c0003t0007g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.926+777G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962539 | |||||||
chr14:75962693 | C | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.926+623G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962693 | |||||||
chr14:75962787 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0097 others(10): Show |
23 | HG00597.hp1 HG01256.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.926+529C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962787 | |||||||
chr14:75962794 | C | G | 1 | a0001c0001t0016g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.926+522G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962794 | |||||||
chr14:75962986 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0136 others(3): Show |
8 | HG02109.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.926+330A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75962986 | |||||||
chr14:75963026 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.926+290G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75963026 | |||||||
chr14:75963128 | C | T | 7 | a0001c0001t0001g0096 a0001c0001t0001g0182 a0001c0001t0001g0190 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.926+188G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75963128 | |||||||
chr14:75963167 | CTG | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0119 a0001c0001t0001g0127 |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+147_926+148del others(2): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75963167 | |||||||
chr14:75963212 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.926+104G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 5/6 | chr14 | 75963212 | |||||||
chr14:75963525 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0037 others(41): Show |
59 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.755-38T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963525 | |||||||
chr14:75963561 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.755-74C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963561 | |||||||
chr14:75963612 | G | A | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.755-125C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963612 | |||||||
chr14:75963794 | T | G | 1 | a0001c0003t0007g0058 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-307A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963794 | |||||||
chr14:75963874 | A | ATTTG | 32 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(29): Show |
45 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.755-391_755-388dup others(4): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963874 | |||||||
chr14:75963874 | A | ATTTGTTT others(1): Show |
6 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-395_755-388dup others(8): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963874 | |||||||
chr14:75963907 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0037 others(19): Show |
33 | HG00438.hp2 HG00642.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.755-420G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963907 | |||||||
chr14:75963918 | C | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.755-431G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963918 | |||||||
chr14:75963937 | C | T | 1 | a0001c0001t0004g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.755-450G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75963937 | |||||||
chr14:75964096 | G | A | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.755-609C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964096 | |||||||
chr14:75964165 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0037 others(35): Show |
52 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.755-678A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964165 | |||||||
chr14:75964201 | C | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0037 others(16): Show |
30 | HG00438.hp2 HG00642.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.755-714G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964201 | |||||||
chr14:75964467 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.755-980T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964467 | |||||||
chr14:75964470 | A | C | 1 | a0001c0003t0007g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.755-983T>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964470 | |||||||
chr14:75964543 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | NA18951.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.754+1045C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964543 | |||||||
chr14:75964650 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0037 others(35): Show |
52 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.754+938A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964650 | |||||||
chr14:75964666 | C | T | 1 | a0001c0001t0020g0108 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.754+922G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964666 | |||||||
chr14:75964763 | G | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0217 |
3 | HG02451.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.754+825C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964763 | |||||||
chr14:75964890 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0230 |
3 | HG01981.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.754+698A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75964890 | |||||||
chr14:75965190 | T | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0037 others(40): Show |
57 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.754+398A>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965190 | |||||||
chr14:75965295 | A | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0120 |
4 | HG01168.hp2 HG02004.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+293T>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965295 | |||||||
chr14:75965302 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.754+286T>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965302 | |||||||
chr14:75965331 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.754+257A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965331 | |||||||
chr14:75965387 | T | C | 2 | a0001c0001t0021g0099 a0001c0003t0007g0175 |
2 | HG02280.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.754+201A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965387 | |||||||
chr14:75965449 | T | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0090 others(11): Show |
20 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.754+139A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965449 | |||||||
chr14:75965465 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.754+123G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 4/6 | chr14 | 75965465 | |||||||
chr14:75965774 | GC | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0020 others(26): Show |
45 | HG00438.hp2 HG00642.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.647-80delG | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75965774 | |||||||
chr14:75965793 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.647-98A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75965793 | |||||||
chr14:75965863 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0119 |
3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.647-168C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75965863 | |||||||
chr14:75965889 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.647-194G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75965889 | |||||||
chr14:75966143 | A | G | 1 | a0001c0001t0017g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.647-448T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966143 | |||||||
chr14:75966177 | C | T | 1 | a0001c0001t0019g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.647-482G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966177 | |||||||
chr14:75966251 | A | T | 1 | a0001c0003t0007g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.647-556T>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966251 | |||||||
chr14:75966272 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.647-577C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966272 | |||||||
chr14:75966286 | A | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(13): Show |
26 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.647-591T>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966286 | |||||||
chr14:75966381 | T | C | 1 | a0001c0001t0006g0085 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.647-686A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966381 | |||||||
chr14:75966441 | G | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(11): Show |
24 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.647-746C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966441 | |||||||
chr14:75966480 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.647-785C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966480 | |||||||
chr14:75966585 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.647-890T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966585 | |||||||
chr14:75966656 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.647-961C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75966656 | |||||||
chr14:75967732 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.647-2037A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75967732 | |||||||
chr14:75967808 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.647-2113A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75967808 | |||||||
chr14:75967889 | G | T | 1 | a0001c0001t0001g0208 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.647-2194C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75967889 | |||||||
chr14:75967961 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0074 a0001c0001t0005g0075 |
4 | HG01175.hp1 HG01257.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-2266G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75967961 | |||||||
chr14:75968543 | T | G | 1 | a0001c0003t0007g0058 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.646+2583A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968543 | |||||||
chr14:75968625 | C | G | 15 | a0001c0001t0001g0151 a0001c0001t0001g0180 a0001c0001t0001g0182 others(12): Show |
15 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.646+2501G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968625 | |||||||
chr14:75968658 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0117 |
4 | HG02071.hp2 NA18612.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+2468G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968658 | |||||||
chr14:75968707 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.646+2419C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968707 | |||||||
chr14:75968795 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0174 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.646+2331G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968795 | |||||||
chr14:75968810 | T | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
13 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.646+2316A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968810 | |||||||
chr14:75968976 | G | A | 1 | a0001c0001t0017g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646+2150C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968976 | |||||||
chr14:75968978 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.646+2148C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75968978 | |||||||
chr14:75969264 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.646+1862C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75969264 | |||||||
chr14:75969432 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.646+1694T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75969432 | |||||||
chr14:75969522 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.646+1604C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75969522 | |||||||
chr14:75969562 | T | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0180 a0001c0001t0001g0187 others(7): Show |
10 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.646+1564A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75969562 | |||||||
chr14:75969602 | G | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(8): Show |
20 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.646+1524C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75969602 | |||||||
chr14:75969679 | A | G | 1 | a0001c0001t0007g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.646+1447T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75969679 | |||||||
chr14:75970095 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.646+1031G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970095 | |||||||
chr14:75970287 | C | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.646+839G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970287 | |||||||
chr14:75970411 | T | C | 1 | a0001c0001t0010g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.646+715A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970411 | |||||||
chr14:75970489 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.646+637C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970489 | |||||||
chr14:75970514 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0020g0108 others(1): Show |
4 | HG02809.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+612C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970514 | |||||||
chr14:75970562 | A | AAAT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0084 others(2): Show |
7 | HG02559.hp1 HG02735.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.646+561_646+563dup others(3): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAAT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
123 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.646+561_646+563del others(3): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAATAAT | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
154 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.646+558_646+563del others(6): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAATAATA others(2): Show |
A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0015 others(14): Show |
17 | HG01106.hp1 HG01257.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.646+555_646+563del others(9): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAATAATA others(5): Show |
A | 3 | a0001c0001t0019g0106 a0001c0001t0020g0108 a0001c0002t0001g0030 |
3 | HG03540.hp2 HG04199.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.646+552_646+563del others(12): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAATAATA others(8): Show |
A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0001g0151 others(6): Show |
9 | HG02451.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.646+549_646+563del others(15): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAATAATA others(11): Show |
A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0180 |
2 | HG03927.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.646+546_646+563del others(18): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970562 | AAATAATA others(14): Show |
A | 1 | a0001c0001t0001g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.646+543_646+563del others(21): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970562 | |||||||
chr14:75970650 | C | CTCCCCTC others(4): Show |
116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.646+465_646+475dup others(11): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970650 | |||||||
chr14:75970650 | C | CTCCCCTC others(15): Show |
4 | a0001c0001t0001g0019 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
6 | HG02109.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.646+475_646+476ins others(22): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970650 | |||||||
chr14:75970696 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.646+430C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970696 | |||||||
chr14:75970740 | C | T | 10 | a0001c0001t0001g0151 a0001c0001t0001g0180 a0001c0001t0001g0187 others(7): Show |
10 | HG02451.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.646+386G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970740 | |||||||
chr14:75970785 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.646+341A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970785 | |||||||
chr14:75970912 | G | T | 1 | a0001c0004t0001g0225 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.646+214C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970912 | |||||||
chr14:75970934 | C | T | 1 | a0001c0001t0010g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.646+192G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75970934 | |||||||
chr14:75971066 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.646+60G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 3/6 | chr14 | 75971066 | |||||||
chr14:75971261 | G | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0135 |
3 | NA18960.hp1 NA19058.hp2 NA19072.hp1 |
splice_region_variant&intron_variant | LOW | c.517-6C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 2/6 | chr14 | 75971261 | |||||||
chr14:75971271 | A | G | 1 | a0001c0001t0001g0042 | 2 | NA18969.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.517-16T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 2/6 | chr14 | 75971271 | |||||||
chr14:75971420 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0078 others(1): Show |
6 | HG01081.hp1 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+135T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 2/6 | chr14 | 75971420 | |||||||
chr14:75971469 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.516+86G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 2/6 | chr14 | 75971469 | |||||||
chr14:75971518 | C | T | 1 | a0001c0001t0011g0188 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.516+37G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 2/6 | chr14 | 75971518 | |||||||
chr14:75971847 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.353-129G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75971847 | |||||||
chr14:75972265 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0020g0108 others(1): Show |
4 | HG02809.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-547A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972265 | |||||||
chr14:75972591 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.353-873C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972591 | |||||||
chr14:75972657 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.353-939G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972657 | |||||||
chr14:75972671 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.353-953C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972671 | |||||||
chr14:75972722 | T | A | 1 | a0001c0001t0005g0075 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.353-1004A>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972722 | |||||||
chr14:75972781 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
6 | HG02109.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-1063A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972781 | |||||||
chr14:75972811 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(7): Show |
19 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.353-1093G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972811 | |||||||
chr14:75972832 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.353-1114T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972832 | |||||||
chr14:75972865 | T | A | 1 | a0001c0001t0001g0040 | 2 | NA18992.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.353-1147A>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75972865 | |||||||
chr14:75973002 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.353-1284C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973002 | |||||||
chr14:75973149 | C | A | 1 | a0001c0001t0001g0049 | 2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.353-1431G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973149 | |||||||
chr14:75973152 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.353-1434C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973152 | |||||||
chr14:75973226 | C | T | 1 | a0001c0001t0010g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.353-1508G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973226 | |||||||
chr14:75973291 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.353-1573G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973291 | |||||||
chr14:75973554 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0050 a0001c0001t0004g0092 others(2): Show |
8 | HG01891.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.353-1836C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973554 | |||||||
chr14:75973650 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.353-1932C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973650 | |||||||
chr14:75973693 | G | C | 1 | a0001c0001t0010g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.353-1975C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973693 | |||||||
chr14:75973877 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.353-2159G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973877 | |||||||
chr14:75973907 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(7): Show |
19 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.353-2189G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973907 | |||||||
chr14:75973937 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.353-2219A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75973937 | |||||||
chr14:75974106 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.353-2388G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974106 | |||||||
chr14:75974317 | T | G | 6 | a0001c0001t0001g0180 a0001c0001t0001g0187 a0001c0001t0001g0189 others(3): Show |
6 | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-2599A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974317 | |||||||
chr14:75974324 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.353-2606T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974324 | |||||||
chr14:75974371 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0140 |
2 | NA18942.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.353-2653A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974371 | |||||||
chr14:75974424 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0020g0108 others(1): Show |
4 | HG02809.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-2706C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974424 | |||||||
chr14:75974434 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.353-2716C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974434 | |||||||
chr14:75974593 | C | T | 1 | a0001c0001t0007g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.353-2875G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974593 | |||||||
chr14:75974764 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.353-3047dupT | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974764 | |||||||
chr14:75974776 | A | AG | 4 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0020g0108 others(1): Show |
4 | HG02809.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-3059_353-3058i others(3): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974776 | |||||||
chr14:75974779 | A | AAAAG | 9 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(6): Show |
18 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.353-3062_353-3061i others(6): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974779 | |||||||
chr14:75974824 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0103 others(6): Show |
13 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.353-3106G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974824 | |||||||
chr14:75974842 | G | C | 1 | a0001c0001t0005g0171 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.353-3124C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974842 | |||||||
chr14:75974955 | G | T | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.353-3237C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75974955 | |||||||
chr14:75975125 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.353-3407A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75975125 | |||||||
chr14:75975221 | A | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.353-3503T>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75975221 | |||||||
chr14:75975368 | A | AAAAATT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.353-3656_353-3651d others(8): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75975368 | |||||||
chr14:75975819 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0174 others(1): Show |
4 | HG00544.hp2 NA18942.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.353-4101C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75975819 | |||||||
chr14:75975967 | T | C | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.353-4249A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75975967 | |||||||
chr14:75976019 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(6): Show |
18 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.353-4301G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976019 | |||||||
chr14:75976130 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.352+4412C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976130 | |||||||
chr14:75976504 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.352+4038C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976504 | |||||||
chr14:75976738 | A | G | 1 | a0001c0001t0021g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.352+3804T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976738 | |||||||
chr14:75976814 | G | T | 1 | a0001c0001t0001g0218 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.352+3728C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976814 | |||||||
chr14:75976815 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.352+3727G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976815 | |||||||
chr14:75976926 | T | G | 1 | a0001c0001t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352+3616A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75976926 | |||||||
chr14:75977205 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.352+3337G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977205 | |||||||
chr14:75977206 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(7): Show |
19 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.352+3336C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977206 | |||||||
chr14:75977236 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.352+3306C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977236 | |||||||
chr14:75977405 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(9): Show |
21 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.352+3137T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977405 | |||||||
chr14:75977477 | C | A | 1 | a0001c0001t0002g0062 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.352+3065G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977477 | |||||||
chr14:75977632 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.352+2910A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977632 | |||||||
chr14:75977642 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.352+2900T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977642 | |||||||
chr14:75977650 | C | G | 1 | a0001c0001t0004g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.352+2892G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977650 | |||||||
chr14:75977656 | C | CA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(23): Show |
35 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.352+2885dupT | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977656 | |||||||
chr14:75977829 | T | C | 1 | a0001c0004t0001g0226 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.352+2713A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977829 | |||||||
chr14:75977870 | GTGCTTAA others(5): Show |
G | 1 | a0001c0001t0001g0180 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.352+2660_352+2671d others(14): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977870 | |||||||
chr14:75977886 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0049 others(4): Show |
16 | HG00438.hp2 HG00642.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.352+2656C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977886 | |||||||
chr14:75977910 | T | G | 16 | a0001c0001t0001g0013 a0001c0001t0001g0090 a0001c0001t0001g0091 others(13): Show |
21 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.352+2632A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977910 | |||||||
chr14:75977988 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.352+2554C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75977988 | |||||||
chr14:75978126 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.352+2416A>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978126 | |||||||
chr14:75978251 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.352+2291C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978251 | |||||||
chr14:75978259 | CCT | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
7 | HG01243.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.352+2281_352+2282d others(4): Show |
TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978259 | |||||||
chr14:75978306 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.352+2236G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978306 | |||||||
chr14:75978342 | G | C | 4 | a0001c0001t0004g0021 a0001c0001t0004g0050 a0001c0001t0004g0152 others(1): Show |
7 | HG01891.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+2200C>G | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978342 | |||||||
chr14:75978359 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | NA18973.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.352+2183C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978359 | |||||||
chr14:75978424 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.352+2118G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978424 | |||||||
chr14:75978823 | G | T | 4 | a0001c0001t0001g0093 a0001c0001t0004g0092 a0001c0001t0012g0094 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1719C>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978823 | |||||||
chr14:75978848 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.352+1694G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978848 | |||||||
chr14:75978922 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
6 | HG01243.hp2 HG01884.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.352+1620G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75978922 | |||||||
chr14:75979015 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.352+1527T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979015 | |||||||
chr14:75979269 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0074 others(1): Show |
6 | HG01175.hp1 HG01257.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+1273G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979269 | |||||||
chr14:75979298 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.352+1244G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979298 | |||||||
chr14:75979513 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.352+1029G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979513 | |||||||
chr14:75979678 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.352+864C>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979678 | |||||||
chr14:75979696 | T | TC | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0053 others(22): Show |
32 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.352+845dupG | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979696 | |||||||
chr14:75979698 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.352+844G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979698 | |||||||
chr14:75979704 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0055 |
5 | NA18941.hp1 NA18957.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+838G>T | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979704 | |||||||
chr14:75979704 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
36 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.352+838G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979704 | |||||||
chr14:75979705 | C | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG03239.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.352+837G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979705 | |||||||
chr14:75979707 | C | CA | 3 | a0001c0001t0010g0199 a0001c0004t0001g0225 a0001c0004t0001g0226 |
3 | HG02622.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.352+834dupT | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75979707 | |||||||
chr14:75980178 | T | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0056 others(33): Show |
54 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.352+364A>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75980178 | |||||||
chr14:75980211 | C | T | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.352+331G>A | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75980211 | |||||||
chr14:75980232 | A | G | 1 | a0001c0001t0010g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.352+310T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75980232 | |||||||
chr14:75980306 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
53 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.352+236T>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75980306 | |||||||
chr14:75980346 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.352+196G>C | TGFB3 | ENSG00000119699.8 | transcript | ENST00000238682.8 | protein_coding | 1/6 | chr14 | 75980346 |