Item | Value |
---|---|
geneid | 340348 |
ensemblid | ENSG00000158457.6 |
hgncid | 28743 |
symbol | TSPAN33 |
name | tetraspanin 33 |
refseq_nuc | NM_178562.5 |
refseq_prot | NP_848657.1 |
ensembl_nuc | ENST00000486685.3 |
ensembl_prot | ENSP00000483872.1 |
mane_status | MANE Select |
chr | chr7 |
start | 129144707 |
end | 129169699 |
strand | + |
ver | v1.2 |
region | chr7:129144707-129169699 |
region5000 | chr7:129139707-129174699 |
regionname0 | TSPAN33_chr7_129144707_129169699 |
regionname5000 | TSPAN33_chr7_129139707_129174699 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 283 | 431 | 92 | 68 | 207 | 16 | 46 | 163 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | MARRP others(278): Show |
chr7 | 129139707 | 129174699 |
a0002 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | MARRP others(278): Show |
chr7 | 129139707 | 129174699 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 849 | 429 | 92 | 67 | 206 | 16 | 46 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | ATGGC others(844): Show |
chr7 | 129139707 | 129174699 | ||
a0001c0002 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | ATGGC others(844): Show |
chr7 | 129139707 | 129174699 | ||
a0001c0004 | 0/0 | 849 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | ATGGC others(844): Show |
chr7 | 129139707 | 129174699 | ||
a0002c0003 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | ATGGC others(844): Show |
chr7 | 129139707 | 129174699 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2951 | 121 | 45 | 32 | 26 | 6 | 11 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0002 | 0/1 | 2951 | 76 | 4 | 12 | 40 | 5 | 14 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0003 | 0/0 | 2951 | 74 | 0 | 2 | 69 | 0 | 3 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0004 | 0/0 | 2953 | 43 | 8 | 8 | 24 | 0 | 3 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2948): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0005 | 0/0 | 2973 | 40 | 2 | 4 | 23 | 2 | 9 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0006 | 0/0 | 2973 | 16 | 5 | 5 | 0 | 3 | 3 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0007 | 0/0 | 2973 | 7 | 6 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0008 | 0/0 | 2951 | 7 | 6 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0009 | 0/0 | 2951 | 6 | 0 | 0 | 6 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0010 | 0/0 | 2951 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0011 | 0/0 | 2973 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0012 | 0/0 | 2951 | 3 | 2 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0013 | 0/0 | 2951 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0014 | 0/0 | 2973 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0015 | 0/0 | 2951 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0016 | 0/0 | 2951 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0017 | 0/0 | 2941 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2936): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0018 | 0/0 | 2951 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0019 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0020 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0021 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0022 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0023 | 0/0 | 2951 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0024 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0025 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0026 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0027 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0028 | 0/0 | 2951 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0029 | 0/0 | 2953 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2948): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0030 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0031 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0001t0032 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
a0001c0002t0005 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0001c0004t0005 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2968): Show |
chr7 | 129139707 | 129174699 |
a0002c0003t0003 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | CTGGG others(2946): Show |
chr7 | 129139707 | 129174699 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 4 | 4 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0012 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0014 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0015 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0018 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0001 | 0/0 | 26 | 2 | 5 | 13 | 2 | 4 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0013 | 0/1 | 5 | 0 | 0 | 4 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0030 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0002 | 0/0 | 25 | 0 | 2 | 22 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0003 | 0/0 | 24 | 0 | 6 | 17 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0005 | 0/0 | 6 | 0 | 0 | 3 | 1 | 2 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0026 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0059 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0036 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0007g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0008g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0009g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0010g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0011g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0012g0062 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0012g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0014g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0015g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0015g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0016g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0017g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0018g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0019g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0020g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0021g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0022g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0023g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0024g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0025g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0026g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0027g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0028g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0029g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0030g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0031g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0001t0032g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0001c0004t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
a0002c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0064 | EUR | GBR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0026 | EUR | GBR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00323 | hp2 | a0001 | c0001 | t0006 | g0046 | EUR | FIN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00423 | hp2 | a0001 | c0001 | t0010 | g0134 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00558 | hp2 | a0001 | c0001 | t0026 | g0009 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0059 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0062 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0163 | AMR | PUR | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0037 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0144 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01928 | hp1 | a0001 | c0001 | t0029 | g0214 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0017 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02071 | hp1 | a0001 | c0001 | t0031 | g0120 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02080 | hp2 | a0001 | c0002 | t0005 | g0089 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CDX | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02523 | hp1 | a0001 | c0001 | t0009 | g0164 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0075 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02572 | hp2 | a0001 | c0001 | t0017 | g0127 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02615 | hp1 | a0001 | c0001 | t0023 | g0217 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0125 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0197 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0195 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0091 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02895 | hp2 | a0001 | c0001 | t0017 | g0128 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02976 | hp2 | a0001 | c0001 | t0013 | g0200 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03041 | hp1 | a0001 | c0001 | t0028 | g0151 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0109 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0204 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | ESN | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0076 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03704 | hp1 | a0001 | c0001 | t0021 | g0023 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03834 | hp2 | a0001 | c0001 | t0015 | g0027 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0196 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0102 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0059 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04115 | hp2 | a0001 | c0001 | t0015 | g0105 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18747 | hp1 | a0001 | c0001 | t0010 | g0137 | EAS | CHB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0198 | AFR | YRI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18939 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18940 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18952 | hp1 | a0001 | c0001 | t0032 | g0188 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18953 | hp2 | a0001 | c0001 | t0018 | g0049 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18964 | hp2 | a0001 | c0001 | t0027 | g0086 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18973 | hp1 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18981 | hp1 | a0002 | c0003 | t0003 | g0118 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18982 | hp2 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18983 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18987 | hp2 | a0001 | c0001 | t0030 | g0114 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18991 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18995 | hp1 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19004 | hp2 | a0001 | c0001 | t0020 | g0005 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19006 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19030 | hp1 | a0001 | c0001 | t0025 | g0216 | AFR | LWK | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | LWK | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19065 | hp1 | a0001 | c0001 | t0014 | g0041 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19080 | hp1 | a0001 | c0001 | t0016 | g0061 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19080 | hp2 | a0001 | c0001 | t0018 | g0049 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19081 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19081 | hp2 | a0001 | c0001 | t0014 | g0041 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19083 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19086 | hp2 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19089 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19091 | hp2 | a0001 | c0001 | t0019 | g0033 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | ASW | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20129 | hp2 | a0001 | c0001 | t0013 | g0199 | AFR | ASW | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0037 | EUR | TSI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0005 | EUR | TSI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | TSI | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | GIH | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | GIH | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01123 | hp1 | a0001 | c0004 | t0005 | g0045 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02109 | hp2 | a0001 | c0001 | t0022 | g0210 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0101 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0031 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | USA | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA18955 | hp2 | a0001 | c0001 | t0016 | g0061 | EAS | JPT | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | LWK | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0013 | REF | REF | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | TSPAN33_chr7_129139707_129174699 | TSPAN33 | chr7 | 129139707 | 129174699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:129166849 | C | A | 1 | a0002 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.531C>A | p.Asn177Lys | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 6/8 | 805/2951 | 531/852 | 177/283 | chr7 | 129166849 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:129145007 | C | T | 1 | a0001c0004 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.27C>T | p.Ala9Ala | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/8 | 301/2951 | 27/852 | 9/283 | chr7 | 129145007 | |||
chr7:129164500 | C | A | 1 | a0001c0002 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.390C>A | p.Ile130Ile | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/8 | 664/2951 | 390/852 | 130/283 | chr7 | 129164500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:129144725 | G | C | 1 | a0001c0001t0019 | 1 | NA19091.hp2 | 5_prime_UTR_variant | MODIFIER | c.-256G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/8 | 256 | chr7 | 129144725 | ||||||
chr7:129167891 | T | G | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(5): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*17T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 17 | chr7 | 129167891 | ||||||
chr7:129167945 | G | A | 16 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(13): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*71G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 71 | chr7 | 129167945 | ||||||
chr7:129168012 | G | A | 1 | a0001c0001t0020 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 138 | chr7 | 129168012 | ||||||
chr7:129168051 | A | G | 3 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0016 |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 177 | chr7 | 129168051 | ||||||
chr7:129168066 | C | T | 1 | a0001c0001t0016 | 2 | NA18955.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*192C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 192 | chr7 | 129168066 | ||||||
chr7:129168082 | C | T | 7 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(4): Show |
82 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*208C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 208 | chr7 | 129168082 | ||||||
chr7:129168220 | G | C | 15 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(12): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*346G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 346 | chr7 | 129168220 | ||||||
chr7:129168255 | A | G | 1 | a0001c0001t0032 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 381 | chr7 | 129168255 | ||||||
chr7:129168256 | T | A | 1 | a0001c0001t0030 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 382 | chr7 | 129168256 | ||||||
chr7:129168262 | C | T | 1 | a0001c0001t0023 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 388 | chr7 | 129168262 | ||||||
chr7:129168446 | T | C | 1 | a0001c0001t0021 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*572T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 572 | chr7 | 129168446 | ||||||
chr7:129168465 | A | C | 2 | a0001c0001t0011 a0001c0001t0022 |
5 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*591A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 591 | chr7 | 129168465 | ||||||
chr7:129168491 | G | A | 1 | a0001c0001t0002 | 75 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*617G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 617 | chr7 | 129168491 | ||||||
chr7:129168530 | G | GTA | 2 | a0001c0001t0004 a0001c0001t0029 |
44 | HG00621.hp1 HG00738.hp1 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*658dupTA | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 659 | INFO_REALIGN_3_PRIME | chr7 | 129168530 | |||||
chr7:129168647 | C | T | 6 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0020 others(3): Show |
46 | HG00140.hp2 HG00733.hp2 HG01123.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*773C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 773 | chr7 | 129168647 | ||||||
chr7:129168831 | G | GACTCCAT others(15): Show |
12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(9): Show |
76 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*957_*958insACTCCA others(16): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 958 | chr7 | 129168831 | ||||||
chr7:129168906 | A | C | 2 | a0001c0001t0009 a0001c0001t0018 |
8 | HG02523.hp1 NA18939.hp1 NA18953.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1032A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1032 | chr7 | 129168906 | ||||||
chr7:129168929 | C | T | 1 | a0001c0001t0007 | 7 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1055 | chr7 | 129168929 | ||||||
chr7:129168958 | C | T | 2 | a0001c0001t0012 a0001c0001t0023 |
4 | HG01099.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1084C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1084 | chr7 | 129168958 | ||||||
chr7:129169073 | T | A | 1 | a0001c0001t0013 | 3 | HG02976.hp2 NA18906.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1199T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1199 | chr7 | 129169073 | ||||||
chr7:129169170 | A | G | 1 | a0001c0001t0015 | 2 | HG03834.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1296A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1296 | chr7 | 129169170 | ||||||
chr7:129169198 | C | T | 2 | a0001c0001t0008 a0001c0001t0013 |
10 | HG01943.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1324C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1324 | chr7 | 129169198 | ||||||
chr7:129169226 | T | A | 4 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0016 others(1): Show |
10 | HG00423.hp2 HG02071.hp1 HG03834.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1352T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1352 | chr7 | 129169226 | ||||||
chr7:129169265 | G | T | 1 | a0001c0001t0022 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1391G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1391 | chr7 | 129169265 | ||||||
chr7:129169292 | G | A | 1 | a0001c0001t0029 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1418 | chr7 | 129169292 | ||||||
chr7:129169379 | C | T | 1 | a0001c0001t0028 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1505C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1505 | chr7 | 129169379 | ||||||
chr7:129169445 | C | A | 1 | a0001c0001t0026 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1571C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1571 | chr7 | 129169445 | ||||||
chr7:129169486 | C | T | 1 | a0001c0001t0027 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1612C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1612 | chr7 | 129169486 | ||||||
chr7:129169500 | GGCGGGAA others(3): Show |
G | 1 | a0001c0001t0017 | 2 | HG02572.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1629_*1638delGGGA others(6): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1629 | INFO_REALIGN_3_PRIME | chr7 | 129169500 | |||||
chr7:129169579 | G | A | 1 | a0001c0001t0014 | 2 | NA19065.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1705G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1705 | chr7 | 129169579 | ||||||
chr7:129169596 | G | A | 1 | a0001c0001t0007 | 7 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1722G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 8/8 | 1722 | chr7 | 129169596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:129145120 | C | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0219 a0001c0001t0001g0220 |
4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+38C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145120 | |||||||
chr7:129145123 | C | A | 4 | a0001c0001t0002g0065 a0001c0001t0004g0066 a0001c0001t0006g0037 others(1): Show |
5 | HG00099.hp1 HG01257.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+41C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145123 | |||||||
chr7:129145168 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.102+86C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145168 | |||||||
chr7:129145202 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.102+120G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145202 | |||||||
chr7:129145318 | G | A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(3): Show |
7 | HG00673.hp1 HG02083.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+236G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145318 | |||||||
chr7:129145372 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.102+290A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145372 | |||||||
chr7:129145555 | C | G | 1 | a0001c0001t0023g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.102+473C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145555 | |||||||
chr7:129145570 | C | G | 1 | a0001c0001t0024g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+488C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145570 | |||||||
chr7:129145617 | C | T | 2 | a0001c0001t0023g0217 a0001c0001t0025g0216 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+535C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145617 | |||||||
chr7:129145999 | G | A | 46 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0073 others(43): Show |
80 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.102+917G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129145999 | |||||||
chr7:129146139 | G | A | 1 | a0001c0001t0006g0139 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.102+1057G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146139 | |||||||
chr7:129146379 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.102+1297C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146379 | |||||||
chr7:129146695 | G | A | 1 | a0001c0001t0005g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.102+1613G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146695 | |||||||
chr7:129146766 | G | C | 30 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0080 others(27): Show |
48 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.102+1684G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146766 | |||||||
chr7:129146778 | A | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
56 | HG00423.hp2 HG00621.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.102+1696A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146778 | |||||||
chr7:129146803 | T | G | 1 | a0001c0001t0002g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.102+1721T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146803 | |||||||
chr7:129146938 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102+1856T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129146938 | |||||||
chr7:129147042 | A | G | 1 | a0001c0001t0006g0139 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.102+1960A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147042 | |||||||
chr7:129147124 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.102+2042A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147124 | |||||||
chr7:129147157 | T | TAAAAAAT others(310): Show |
1 | a0001c0001t0005g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.102+2091_102+2092i others(319): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129147157 | ||||||
chr7:129147157 | T | TAAAAAAT others(344): Show |
1 | a0001c0001t0005g0078 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.102+2091_102+2092i others(353): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129147157 | ||||||
chr7:129147298 | C | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0002g0001 others(30): Show |
73 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.102+2216C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147298 | |||||||
chr7:129147306 | G | A | 1 | a0001c0001t0010g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.102+2224G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147306 | |||||||
chr7:129147493 | A | T | 1 | a0001c0001t0002g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.102+2411A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147493 | |||||||
chr7:129147569 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.102+2487A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147569 | |||||||
chr7:129147707 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.102+2625G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147707 | |||||||
chr7:129147751 | G | A | 2 | a0001c0001t0003g0185 a0001c0001t0030g0114 |
2 | HG02040.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.102+2669G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147751 | |||||||
chr7:129147793 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0090 |
3 | HG02683.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.102+2711T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147793 | |||||||
chr7:129147851 | C | G | 2 | a0001c0001t0006g0107 a0001c0001t0006g0108 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.102+2769C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147851 | |||||||
chr7:129147873 | T | G | 81 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(78): Show |
144 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.102+2791T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147873 | |||||||
chr7:129147994 | G | C | 1 | a0001c0001t0023g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.102+2912G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129147994 | |||||||
chr7:129148000 | G | A | 3 | a0001c0001t0010g0027 a0001c0001t0015g0027 a0001c0001t0015g0105 |
4 | HG03834.hp2 HG04115.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+2918G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148000 | |||||||
chr7:129148084 | C | G | 1 | a0001c0001t0006g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.102+3002C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148084 | |||||||
chr7:129148105 | T | C | 1 | a0001c0001t0006g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.102+3023T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148105 | |||||||
chr7:129148161 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
274 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.102+3079C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148161 | |||||||
chr7:129148224 | C | G | 7 | a0001c0001t0002g0065 a0001c0001t0006g0036 a0001c0001t0006g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+3142C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148224 | |||||||
chr7:129148279 | C | G | 1 | a0001c0001t0001g0056 | 2 | HG01069.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.102+3197C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148279 | |||||||
chr7:129148280 | T | A | 1 | a0001c0001t0001g0056 | 2 | HG01069.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.102+3198T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148280 | |||||||
chr7:129148389 | G | C | 39 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(36): Show |
80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.102+3307G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148389 | |||||||
chr7:129148409 | G | A | 1 | a0001c0001t0012g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102+3327G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148409 | |||||||
chr7:129148432 | C | T | 1 | a0001c0001t0011g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.102+3350C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148432 | |||||||
chr7:129148569 | G | A | 1 | a0001c0001t0007g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+3487G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148569 | |||||||
chr7:129148764 | C | G | 1 | a0001c0001t0029g0214 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.102+3682C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129148764 | |||||||
chr7:129149182 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0008g0022 a0001c0001t0008g0074 |
4 | HG02717.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+4100G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149182 | |||||||
chr7:129149227 | C | A | 1 | a0001c0001t0023g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.102+4145C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149227 | |||||||
chr7:129149266 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.102+4184G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149266 | |||||||
chr7:129149286 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
271 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.102+4204G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149286 | |||||||
chr7:129149506 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.102+4424C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149506 | |||||||
chr7:129149598 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.102+4516T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149598 | |||||||
chr7:129149627 | C | T | 7 | a0001c0001t0001g0212 a0001c0001t0004g0011 a0001c0001t0004g0050 others(4): Show |
14 | HG01099.hp1 HG01433.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+4545C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149627 | |||||||
chr7:129149674 | TC | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
272 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.102+4595delC | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129149674 | ||||||
chr7:129149742 | G | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
272 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.102+4660G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149742 | |||||||
chr7:129149747 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
272 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.102+4665G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149747 | |||||||
chr7:129149875 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0220 |
3 | HG02486.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.102+4793G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129149875 | |||||||
chr7:129150043 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
269 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.102+4961G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150043 | |||||||
chr7:129150066 | C | T | 3 | a0001c0001t0010g0027 a0001c0001t0015g0027 a0001c0001t0015g0105 |
4 | HG03834.hp2 HG04115.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+4984C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150066 | |||||||
chr7:129150148 | G | A | 1 | a0001c0001t0006g0107 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102+5066G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150148 | |||||||
chr7:129150266 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+5184C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150266 | |||||||
chr7:129150350 | C | T | 86 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0001t0001g0121 others(83): Show |
153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.102+5268C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150350 | |||||||
chr7:129150399 | A | T | 1 | a0001c0001t0004g0159 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.102+5317A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150399 | |||||||
chr7:129150469 | G | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0071 others(109): Show |
214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.102+5387G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150469 | |||||||
chr7:129150650 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0071 others(112): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.102+5568T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150650 | |||||||
chr7:129150897 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.102+5815C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150897 | |||||||
chr7:129150955 | A | G | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+5873A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129150955 | |||||||
chr7:129151006 | T | A | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+5924T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151006 | |||||||
chr7:129151008 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.102+5926C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151008 | |||||||
chr7:129151105 | C | T | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+6023C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151105 | |||||||
chr7:129151153 | G | A | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+6071G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151153 | |||||||
chr7:129151201 | A | C | 1 | a0001c0001t0003g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.102+6119A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151201 | |||||||
chr7:129151319 | G | A | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+6237G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151319 | |||||||
chr7:129151557 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
336 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.102+6475C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151557 | |||||||
chr7:129151634 | C | A | 1 | a0001c0001t0024g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+6552C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151634 | |||||||
chr7:129151804 | T | G | 3 | a0001c0001t0007g0035 a0001c0001t0007g0101 a0001c0001t0007g0163 |
5 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+6722T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151804 | |||||||
chr7:129151823 | G | A | 1 | a0001c0001t0006g0107 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102+6741G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129151823 | |||||||
chr7:129152287 | G | A | 47 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(44): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.102+7205G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152287 | |||||||
chr7:129152302 | G | A | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+7220G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152302 | |||||||
chr7:129152305 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.102+7223G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152305 | |||||||
chr7:129152316 | G | A | 1 | a0001c0001t0005g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.102+7234G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152316 | |||||||
chr7:129152515 | C | T | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+7433C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152515 | |||||||
chr7:129152539 | T | A | 58 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+7457T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152539 | |||||||
chr7:129152547 | T | G | 1 | a0001c0001t0005g0026 | 3 | HG00140.hp2 HG01346.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.102+7465T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152547 | |||||||
chr7:129152601 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.102+7519C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152601 | |||||||
chr7:129152689 | A | AAAAC | 41 | a0001c0001t0001g0093 a0001c0001t0005g0005 a0001c0001t0005g0023 others(38): Show |
61 | HG00140.hp2 HG00423.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.102+7629_102+7632d others(6): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129152689 | ||||||
chr7:129152689 | AAAAC | A | 3 | a0001c0001t0001g0082 a0001c0001t0003g0028 a0001c0001t0018g0049 |
6 | NA18953.hp2 NA18968.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+7629_102+7632d others(6): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129152689 | ||||||
chr7:129152785 | C | T | 1 | a0001c0001t0006g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.102+7703C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152785 | |||||||
chr7:129152786 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.102+7704G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129152786 | |||||||
chr7:129153026 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102+7944T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153026 | |||||||
chr7:129153059 | CA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.102+8000delA | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129153059 | ||||||
chr7:129153059 | CAA | C | 18 | a0001c0001t0001g0100 a0001c0001t0002g0112 a0001c0001t0002g0156 others(15): Show |
22 | HG00423.hp2 HG02132.hp2 HG02976.hp2 others(19): Show |
intron_variant | MODIFIER | c.102+7999_102+8000d others(4): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129153059 | ||||||
chr7:129153059 | CAAAAAAA | C | 5 | a0001c0001t0007g0035 a0001c0001t0007g0091 a0001c0001t0007g0092 others(2): Show |
7 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+7994_102+8000d others(9): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129153059 | ||||||
chr7:129153059 | CAAAAAAA others(1): Show |
C | 42 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(39): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.102+7993_102+8000d others(10): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129153059 | ||||||
chr7:129153059 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0124 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.102+7989_102+8000d others(14): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129153059 | ||||||
chr7:129153077 | A | G | 7 | a0001c0001t0006g0107 a0001c0001t0011g0031 a0001c0001t0011g0131 others(4): Show |
10 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+7995A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153077 | |||||||
chr7:129153078 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | HG00673.hp1 HG02083.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+7996A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153078 | |||||||
chr7:129153095 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.102+8013G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153095 | |||||||
chr7:129153148 | A | G | 3 | a0001c0001t0011g0031 a0001c0001t0011g0131 a0001c0001t0022g0210 |
5 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+8066A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153148 | |||||||
chr7:129153229 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.102+8147G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153229 | |||||||
chr7:129153428 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0004g0003 a0001c0001t0004g0060 others(8): Show |
35 | HG00621.hp1 HG00738.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.103-8251A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153428 | |||||||
chr7:129153485 | G | A | 1 | a0001c0001t0006g0194 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.103-8194G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153485 | |||||||
chr7:129153595 | T | G | 1 | a0001c0001t0022g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.103-8084T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153595 | |||||||
chr7:129153636 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0162 a0001c0001t0001g0182 others(1): Show |
8 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-8043A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153636 | |||||||
chr7:129153657 | A | AAG | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.103-8020_103-8019d others(4): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129153657 | ||||||
chr7:129153665 | T | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.103-8014T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153665 | |||||||
chr7:129153711 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103-7968C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153711 | |||||||
chr7:129153719 | T | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
342 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.103-7960T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153719 | |||||||
chr7:129153881 | T | C | 7 | a0001c0001t0002g0065 a0001c0001t0006g0036 a0001c0001t0006g0046 others(4): Show |
10 | HG00099.hp1 HG00323.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.103-7798T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153881 | |||||||
chr7:129153901 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103-7778C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153901 | |||||||
chr7:129153913 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.103-7766T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129153913 | |||||||
chr7:129154101 | G | C | 1 | a0001c0001t0006g0037 | 2 | HG01257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.103-7578G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154101 | |||||||
chr7:129154479 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.103-7200C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154479 | |||||||
chr7:129154541 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.103-7138A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154541 | |||||||
chr7:129154611 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0162 a0001c0001t0001g0212 |
7 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-7068C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154611 | |||||||
chr7:129154685 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.103-6994A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154685 | |||||||
chr7:129154729 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0220 |
3 | HG02486.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.103-6950G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154729 | |||||||
chr7:129154777 | G | T | 3 | a0001c0001t0011g0031 a0001c0001t0011g0131 a0001c0001t0022g0210 |
5 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-6902G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154777 | |||||||
chr7:129154805 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.103-6874C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154805 | |||||||
chr7:129154866 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.103-6813A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129154866 | |||||||
chr7:129155126 | T | G | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-6553T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155126 | |||||||
chr7:129155147 | C | T | 38 | a0001c0001t0002g0002 a0001c0001t0003g0002 a0001c0001t0003g0007 others(35): Show |
80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.103-6532C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155147 | |||||||
chr7:129155326 | T | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
342 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.103-6353T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155326 | |||||||
chr7:129155439 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.103-6240A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155439 | |||||||
chr7:129155543 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
342 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.103-6136A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155543 | |||||||
chr7:129155552 | A | G | 1 | a0001c0001t0032g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.103-6127A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155552 | |||||||
chr7:129155656 | GT | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.103-6013delT | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129155656 | ||||||
chr7:129155716 | A | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
336 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.103-5963A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155716 | |||||||
chr7:129155797 | C | T | 1 | a0001c0001t0006g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.103-5882C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155797 | |||||||
chr7:129155845 | C | T | 1 | a0001c0001t0024g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-5834C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155845 | |||||||
chr7:129155932 | C | T | 55 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(52): Show |
79 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.103-5747C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155932 | |||||||
chr7:129155978 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-5701C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155978 | |||||||
chr7:129155979 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.103-5700G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155979 | |||||||
chr7:129155983 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0172 a0001c0001t0001g0179 others(1): Show |
8 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-5696G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129155983 | |||||||
chr7:129156028 | G | T | 13 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0039 others(10): Show |
21 | HG01168.hp2 HG01169.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-5651G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129156028 | |||||||
chr7:129156114 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.103-5565T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129156114 | |||||||
chr7:129156393 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0162 a0001c0001t0001g0182 others(1): Show |
8 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-5286C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129156393 | |||||||
chr7:129156778 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.103-4901C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129156778 | |||||||
chr7:129157063 | C | T | 5 | a0001c0001t0002g0020 a0001c0001t0002g0111 a0001c0001t0002g0158 others(2): Show |
8 | NA18947.hp1 NA18955.hp1 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-4616C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157063 | |||||||
chr7:129157161 | T | C | 47 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(44): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.103-4518T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157161 | |||||||
chr7:129157226 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.103-4453G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157226 | |||||||
chr7:129157296 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.103-4383A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157296 | |||||||
chr7:129157577 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.103-4102G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157577 | |||||||
chr7:129157585 | C | T | 47 | a0001c0001t0002g0065 a0001c0001t0005g0005 a0001c0001t0005g0023 others(44): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.103-4094C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157585 | |||||||
chr7:129157781 | C | G | 15 | a0001c0001t0002g0065 a0001c0001t0006g0036 a0001c0001t0006g0037 others(12): Show |
21 | HG00099.hp1 HG00323.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-3898C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157781 | |||||||
chr7:129157858 | C | T | 1 | a0001c0001t0024g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-3821C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157858 | |||||||
chr7:129157960 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0166 |
4 | HG00639.hp1 HG00741.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3719G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157960 | |||||||
chr7:129157968 | A | T | 1 | a0001c0001t0005g0042 | 2 | NA18950.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.103-3711A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157968 | |||||||
chr7:129157977 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.103-3702A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157977 | |||||||
chr7:129157981 | C | T | 1 | a0001c0001t0024g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-3698C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129157981 | |||||||
chr7:129158006 | G | A | 1 | a0001c0001t0025g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-3673G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158006 | |||||||
chr7:129158050 | C | T | 1 | a0001c0001t0010g0137 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.103-3629C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158050 | |||||||
chr7:129158086 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0162 a0001c0001t0001g0176 others(2): Show |
9 | HG01496.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-3593G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158086 | |||||||
chr7:129158124 | T | TCTCCTTC others(20): Show |
1 | a0001c0001t0009g0169 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.103-3546_103-3520d others(29): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129158124 | ||||||
chr7:129158213 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | HG00673.hp1 HG02083.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3466A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158213 | |||||||
chr7:129158258 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.103-3421A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158258 | |||||||
chr7:129158315 | C | G | 4 | a0001c0001t0006g0107 a0001c0001t0012g0062 a0001c0001t0012g0204 others(1): Show |
5 | HG01099.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-3364C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158315 | |||||||
chr7:129158527 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0004g0003 a0001c0001t0004g0011 others(11): Show |
44 | HG00621.hp1 HG00738.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.103-3152G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158527 | |||||||
chr7:129158894 | G | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0025 others(14): Show |
32 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.103-2785G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129158894 | |||||||
chr7:129159040 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.103-2639C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159040 | |||||||
chr7:129159068 | C | CT | 3 | a0001c0001t0004g0011 a0001c0001t0004g0050 a0001c0001t0004g0211 |
9 | HG01433.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-2602dupT | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129159068 | ||||||
chr7:129159141 | A | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
337 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.103-2538A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159141 | |||||||
chr7:129159146 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0008g0017 a0001c0001t0008g0022 others(2): Show |
9 | HG01943.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-2533C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159146 | |||||||
chr7:129159294 | C | T | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-2385C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159294 | |||||||
chr7:129159305 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
337 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.103-2374C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159305 | |||||||
chr7:129159322 | T | C | 1 | a0001c0001t0022g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.103-2357T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159322 | |||||||
chr7:129159579 | T | C | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-2100T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159579 | |||||||
chr7:129159733 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0007g0092 |
2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.103-1946C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129159733 | |||||||
chr7:129160564 | T | C | 1 | a0001c0001t0025g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-1115T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129160564 | |||||||
chr7:129160609 | A | G | 2 | a0001c0001t0003g0133 a0001c0001t0031g0120 |
2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.103-1070A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129160609 | |||||||
chr7:129160765 | G | A | 3 | a0001c0001t0012g0062 a0001c0001t0012g0204 a0001c0001t0023g0217 |
4 | HG01099.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-914G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129160765 | |||||||
chr7:129160792 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-887G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129160792 | |||||||
chr7:129160855 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
341 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.103-824G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129160855 | |||||||
chr7:129161045 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.103-634C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129161045 | |||||||
chr7:129161097 | G | A | 1 | a0001c0001t0002g0053 | 2 | NA18965.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.103-582G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129161097 | |||||||
chr7:129161180 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-499C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129161180 | |||||||
chr7:129161593 | TCTC | T | 3 | a0001c0001t0011g0031 a0001c0001t0011g0131 a0001c0001t0022g0210 |
5 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-83_103-81delCC others(1): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 129161593 | ||||||
chr7:129161614 | T | C | 3 | a0001c0001t0012g0062 a0001c0001t0012g0204 a0001c0001t0023g0217 |
4 | HG01099.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-65T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 1/7 | chr7 | 129161614 | |||||||
chr7:129161874 | G | A | 47 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(44): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.160+138G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 2/7 | chr7 | 129161874 | |||||||
chr7:129162115 | T | G | 1 | a0001c0001t0014g0041 | 2 | NA19065.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.161-279T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 2/7 | chr7 | 129162115 | |||||||
chr7:129162271 | C | T | 3 | a0001c0001t0011g0031 a0001c0001t0011g0131 a0001c0001t0022g0210 |
5 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-123C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 2/7 | chr7 | 129162271 | |||||||
chr7:129162540 | A | T | 2 | a0001c0001t0001g0097 a0001c0001t0028g0151 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.288+19A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 3/7 | chr7 | 129162540 | |||||||
chr7:129162685 | C | T | 58 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.289-148C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 3/7 | chr7 | 129162685 | |||||||
chr7:129162782 | G | A | 1 | a0001c0001t0015g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.289-51G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 3/7 | chr7 | 129162782 | |||||||
chr7:129162809 | C | A | 1 | a0001c0001t0002g0150 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.289-24C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 3/7 | chr7 | 129162809 | |||||||
chr7:129162818 | C | G | 1 | a0001c0001t0006g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.289-15C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 3/7 | chr7 | 129162818 | |||||||
chr7:129163048 | A | G | 1 | a0001c0001t0003g0190 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.363+141A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163048 | |||||||
chr7:129163068 | T | C | 1 | a0001c0001t0013g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.363+161T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163068 | |||||||
chr7:129163095 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
342 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.363+188T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163095 | |||||||
chr7:129163188 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0172 a0001c0001t0001g0179 others(1): Show |
8 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+281G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163188 | |||||||
chr7:129163244 | T | G | 1 | a0001c0001t0006g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363+337T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163244 | |||||||
chr7:129163296 | A | T | 1 | a0001c0001t0031g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.363+389A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163296 | |||||||
chr7:129163333 | C | CT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(127): Show |
263 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.363+443dupT | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 129163333 | ||||||
chr7:129163333 | C | CTT | 12 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0141 others(9): Show |
19 | HG01099.hp1 HG01168.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.363+442_363+443dup others(2): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 129163333 | ||||||
chr7:129163333 | C | CTTT | 5 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0002g0157 others(2): Show |
6 | HG01934.hp1 HG02738.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+441_363+443dup others(3): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 129163333 | ||||||
chr7:129163333 | C | CTTTT | 45 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(42): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.363+440_363+443dup others(4): Show |
TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 129163333 | ||||||
chr7:129163487 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.363+580C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163487 | |||||||
chr7:129163502 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.363+595T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163502 | |||||||
chr7:129163530 | G | T | 2 | a0001c0001t0003g0072 a0001c0001t0003g0123 |
2 | NA18957.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.363+623G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163530 | |||||||
chr7:129163586 | A | G | 1 | a0001c0001t0003g0119 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.363+679A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163586 | |||||||
chr7:129163663 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0008g0022 a0001c0001t0008g0074 |
4 | HG02717.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+756T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163663 | |||||||
chr7:129163682 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.363+775T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163682 | |||||||
chr7:129163786 | C | G | 1 | a0001c0001t0005g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.364-688C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163786 | |||||||
chr7:129163965 | A | T | 1 | a0002c0003t0003g0118 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.364-509A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129163965 | |||||||
chr7:129164200 | A | G | 58 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(55): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.364-274A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129164200 | |||||||
chr7:129164272 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.364-202G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129164272 | |||||||
chr7:129164328 | C | T | 1 | a0001c0001t0017g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.364-146C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129164328 | |||||||
chr7:129164352 | C | T | 47 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(44): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.364-122C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129164352 | |||||||
chr7:129164377 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
342 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.364-97G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 4/7 | chr7 | 129164377 | |||||||
chr7:129164576 | G | A | 1 | a0001c0001t0004g0211 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.459+7G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129164576 | |||||||
chr7:129164633 | T | C | 47 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(44): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.459+64T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129164633 | |||||||
chr7:129164710 | C | T | 3 | a0001c0001t0011g0031 a0001c0001t0011g0131 a0001c0001t0022g0210 |
5 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+141C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129164710 | |||||||
chr7:129164740 | A | G | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+171A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129164740 | |||||||
chr7:129164939 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
338 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.459+370C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129164939 | |||||||
chr7:129165018 | C | A | 1 | a0002c0003t0003g0118 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.459+449C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165018 | |||||||
chr7:129165019 | A | T | 1 | a0002c0003t0003g0118 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.459+450A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165019 | |||||||
chr7:129165091 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.459+522C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165091 | |||||||
chr7:129165204 | C | G | 3 | a0001c0001t0012g0062 a0001c0001t0012g0204 a0001c0001t0023g0217 |
4 | HG01099.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+635C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165204 | |||||||
chr7:129165395 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0028g0151 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.459+826G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165395 | |||||||
chr7:129165606 | A | G | 1 | a0001c0001t0003g0165 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.459+1037A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165606 | |||||||
chr7:129165741 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.460-1037T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165741 | |||||||
chr7:129165929 | A | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-849A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165929 | |||||||
chr7:129165931 | A | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-847A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165931 | |||||||
chr7:129165933 | A | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-845A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165933 | |||||||
chr7:129165934 | A | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-844A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165934 | |||||||
chr7:129165935 | G | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-843G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165935 | |||||||
chr7:129165938 | A | C | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-840A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165938 | |||||||
chr7:129165940 | C | CT | 28 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0026 others(25): Show |
44 | HG00140.hp2 HG00733.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.460-828dupT | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 129165940 | ||||||
chr7:129165940 | CT | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
341 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.460-828delT | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 129165940 | ||||||
chr7:129165947 | T | C | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-831T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165947 | |||||||
chr7:129165959 | C | T | 1 | a0001c0001t0008g0074 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-819C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165959 | |||||||
chr7:129165974 | T | C | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-804T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129165974 | |||||||
chr7:129166009 | C | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-769C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166009 | |||||||
chr7:129166023 | G | A | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-755G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166023 | |||||||
chr7:129166030 | G | A | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-748G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166030 | |||||||
chr7:129166031 | G | A | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-747G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166031 | |||||||
chr7:129166039 | T | C | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-739T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166039 | |||||||
chr7:129166040 | G | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-738G>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166040 | |||||||
chr7:129166042 | A | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-736A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166042 | |||||||
chr7:129166047 | C | T | 7 | a0001c0001t0010g0027 a0001c0001t0010g0126 a0001c0001t0010g0134 others(4): Show |
9 | HG00423.hp2 HG03834.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-731C>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166047 | |||||||
chr7:129166055 | A | C | 1 | a0001c0001t0002g0110 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.460-723A>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166055 | |||||||
chr7:129166081 | G | C | 3 | a0001c0001t0005g0023 a0001c0001t0005g0102 a0001c0001t0021g0023 |
4 | HG03017.hp1 HG03704.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-697G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166081 | |||||||
chr7:129166084 | C | G | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-694C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166084 | |||||||
chr7:129166086 | T | C | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-692T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166086 | |||||||
chr7:129166097 | G | C | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-681G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166097 | |||||||
chr7:129166100 | C | A | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-678C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166100 | |||||||
chr7:129166101 | A | G | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-677A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166101 | |||||||
chr7:129166124 | A | G | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-654A>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166124 | |||||||
chr7:129166128 | T | A | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-650T>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166128 | |||||||
chr7:129166137 | G | C | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-641G>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166137 | |||||||
chr7:129166138 | C | A | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-640C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166138 | |||||||
chr7:129166139 | A | T | 1 | a0001c0001t0005g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.460-639A>T | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166139 | |||||||
chr7:129166187 | T | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.460-591T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166187 | |||||||
chr7:129166216 | C | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
342 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.460-562C>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166216 | |||||||
chr7:129166381 | T | C | 1 | a0001c0001t0025g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-397T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166381 | |||||||
chr7:129166617 | G | A | 1 | a0001c0001t0023g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.460-161G>A | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 5/7 | chr7 | 129166617 | |||||||
chr7:129167056 | T | G | 1 | a0001c0001t0005g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.588+150T>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 6/7 | chr7 | 129167056 | |||||||
chr7:129167330 | T | C | 1 | a0001c0001t0003g0191 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.589-69T>C | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 6/7 | chr7 | 129167330 | |||||||
chr7:129167729 | C | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0166 others(3): Show |
12 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.751-44C>G | TSPAN33 | ENSG00000158457.6 | transcript | ENST00000486685.3 | protein_coding | 7/7 | chr7 | 129167729 |