Item | Value |
---|---|
geneid | 1950 |
ensemblid | ENSG00000138798.13 |
hgncid | 3229 |
symbol | EGF |
name | epidermal growth factor |
refseq_nuc | NM_001963.6 |
refseq_prot | NP_001954.2 |
ensembl_nuc | ENST00000265171.10 |
ensembl_prot | ENSP00000265171.5 |
mane_status | MANE Select |
chr | chr4 |
start | 109912883 |
end | 110013766 |
strand | + |
ver | v1.2 |
region | chr4:109912883-110013766 |
region5000 | chr4:109907883-110018766 |
regionname0 | EGF_chr4_109912883_110013766 |
regionname5000 | EGF_chr4_109907883_110018766 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1207 | 142 | 41 | 25 | 62 | 3 | 11 | 49 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0002 | 0/0 | 1207 | 81 | 7 | 17 | 43 | 5 | 9 | 32 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0003 | 0/0 | 1152 | 44 | 0 | 0 | 36 | 0 | 8 | 25 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1147): Show |
chr4 | 109907883 | 110018766 |
a0004 | 0/0 | 1207 | 40 | 1 | 5 | 29 | 1 | 4 | 24 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0005 | 0/0 | 1207 | 20 | 16 | 2 | 2 | 0 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0006 | 1/0 | 1207 | 14 | 1 | 5 | 0 | 1 | 6 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0007 | 0/0 | 1207 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0008 | 0/0 | 1207 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0009 | 0/0 | 1207 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0010 | 0/0 | 1207 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0011 | 0/0 | 1207 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0012 | 0/0 | 1207 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0013 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0014 | 0/0 | 1152 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1147): Show |
chr4 | 109907883 | 110018766 |
a0015 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0016 | 0/0 | 1207 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0017 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(671): Show |
chr4 | 109907883 | 110018766 |
a0018 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0019 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0020 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0021 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0022 | 0/0 | 1223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1218): Show |
chr4 | 109907883 | 110018766 |
a0023 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0024 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0025 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0026 | 0/0 | 1207 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
a0027 | 0/1 | 1207 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | MLLTL others(1202): Show |
chr4 | 109907883 | 110018766 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3621 | 124 | 39 | 21 | 58 | 0 | 6 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0007 | 0/0 | 3621 | 8 | 0 | 3 | 0 | 2 | 3 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0013 | 0/0 | 3621 | 3 | 0 | 0 | 0 | 1 | 2 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0016 | 0/0 | 3621 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0019 | 0/0 | 3621 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0026 | 0/0 | 3621 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0027 | 0/0 | 3621 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0001c0033 | 0/0 | 3621 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0002c0002 | 0/0 | 3621 | 81 | 7 | 17 | 43 | 5 | 9 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0003c0003 | 0/0 | 3622 | 44 | 0 | 0 | 36 | 0 | 8 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3617): Show |
chr4 | 109907883 | 110018766 | ||
a0004c0004 | 0/0 | 3621 | 39 | 1 | 5 | 29 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0004c0032 | 0/0 | 3621 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0005c0005 | 0/0 | 3621 | 20 | 16 | 2 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0006c0006 | 1/0 | 3621 | 14 | 1 | 5 | 0 | 1 | 6 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0007c0008 | 0/0 | 3621 | 7 | 0 | 0 | 7 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0008c0009 | 0/0 | 3621 | 7 | 0 | 0 | 7 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0009c0010 | 0/0 | 3621 | 5 | 4 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0010c0011 | 0/0 | 3621 | 4 | 0 | 0 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0011c0012 | 0/0 | 3621 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0012c0014 | 0/0 | 3621 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0013c0017 | 0/0 | 3621 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0014c0015 | 0/0 | 3622 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3617): Show |
chr4 | 109907883 | 110018766 | ||
a0015c0018 | 0/0 | 3621 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0016c0030 | 0/0 | 3621 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0017c0031 | 0/0 | 3622 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3617): Show |
chr4 | 109907883 | 110018766 | ||
a0018c0023 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0019c0034 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0020c0029 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0021c0025 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0022c0035 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3664): Show |
chr4 | 109907883 | 110018766 | ||
a0023c0024 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0024c0022 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0025c0028 | 0/0 | 3621 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0026c0020 | 0/0 | 3621 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 | ||
a0027c0021 | 0/1 | 3621 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | ATGCT others(3616): Show |
chr4 | 109907883 | 110018766 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6387 | 36 | 6 | 10 | 16 | 0 | 4 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0003 | 0/0 | 6387 | 3 | 0 | 0 | 3 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0004 | 0/0 | 6387 | 32 | 4 | 8 | 19 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0006 | 0/0 | 6388 | 9 | 1 | 1 | 6 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0007 | 0/0 | 6387 | 6 | 6 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0011 | 0/0 | 6387 | 7 | 7 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0012 | 0/0 | 6387 | 4 | 2 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0013 | 0/0 | 6388 | 5 | 0 | 1 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0014 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0015 | 0/0 | 6387 | 4 | 2 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0018 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0020 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0022 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0025 | 0/0 | 6387 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0027 | 0/0 | 6387 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0028 | 0/0 | 6386 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6381): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0029 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0030 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0033 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6381): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0034 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0040 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0001t0044 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0007t0002 | 0/0 | 6387 | 8 | 0 | 3 | 0 | 2 | 3 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0013t0002 | 0/0 | 6387 | 2 | 0 | 0 | 0 | 1 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0013t0006 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0016t0002 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0016t0006 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0001c0019t0007 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0019t0017 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6381): Show |
chr4 | 109907883 | 110018766 |
a0001c0026t0002 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0027t0004 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0001c0033t0004 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0001 | 0/0 | 6388 | 54 | 4 | 13 | 29 | 3 | 5 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0002 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0006 | 0/0 | 6388 | 8 | 0 | 2 | 5 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0009 | 0/0 | 6389 | 8 | 1 | 2 | 4 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0012 | 0/0 | 6387 | 2 | 0 | 0 | 1 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0015 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0021 | 0/0 | 6389 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0023 | 0/0 | 6388 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0035 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0036 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0002c0002t0043 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0003c0003t0005 | 0/0 | 6389 | 26 | 0 | 0 | 21 | 0 | 5 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0003c0003t0008 | 0/0 | 6390 | 14 | 0 | 0 | 12 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6385): Show |
chr4 | 109907883 | 110018766 |
a0003c0003t0018 | 0/0 | 6389 | 2 | 0 | 0 | 1 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0003c0003t0026 | 0/0 | 6389 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0004c0004t0003 | 0/0 | 6387 | 28 | 1 | 4 | 21 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0004c0004t0004 | 0/0 | 6387 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0004c0004t0006 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0004c0004t0010 | 0/0 | 6388 | 7 | 0 | 1 | 5 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0004c0004t0039 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0004c0032t0003 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0004 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0006 | 0/0 | 6388 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0007 | 0/0 | 6387 | 5 | 5 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0011 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0013 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0017 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6381): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0019 | 0/0 | 6387 | 4 | 4 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0024 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0038 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0041 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0005c0005t0046 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0006c0006t0001 | 1/0 | 6388 | 12 | 1 | 4 | 0 | 1 | 5 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0006c0006t0009 | 0/0 | 6389 | 2 | 0 | 1 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0007c0008t0003 | 0/0 | 6387 | 5 | 0 | 0 | 5 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0007c0008t0006 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0007c0008t0032 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0008c0009t0001 | 0/0 | 6388 | 6 | 0 | 0 | 6 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0008c0009t0009 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0009c0010t0016 | 0/0 | 6387 | 4 | 3 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0009c0010t0042 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0010c0011t0001 | 0/0 | 6388 | 4 | 0 | 0 | 4 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0011c0012t0014 | 0/0 | 6387 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0012c0014t0007 | 0/0 | 6387 | 3 | 3 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0013c0017t0007 | 0/0 | 6387 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0014c0015t0005 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0014c0015t0018 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0015c0018t0017 | 0/0 | 6386 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6381): Show |
chr4 | 109907883 | 110018766 |
a0016c0030t0016 | 0/0 | 6387 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0017c0031t0005 | 0/0 | 6389 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0018c0023t0045 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0019c0034t0020 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0020c0029t0031 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0021c0025t0021 | 0/0 | 6389 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6384): Show |
chr4 | 109907883 | 110018766 |
a0022c0035t0017 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6429): Show |
chr4 | 109907883 | 110018766 |
a0023c0024t0007 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6382): Show |
chr4 | 109907883 | 110018766 |
a0024c0022t0006 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0025c0028t0001 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0026c0020t0010 | 0/0 | 6388 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
a0027c0021t0037 | 0/1 | 6388 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | CAAAA others(6383): Show |
chr4 | 109907883 | 110018766 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0006g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0007g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0012g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0012g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0012g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0013g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0013g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0013g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0013g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0013g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0015g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0015g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0015g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0018g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0020g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0020g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0022g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0022g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0025g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0025g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0027g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0027g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0028g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0029g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0030g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0033g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0034g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0040g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0001t0044g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0007t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0013t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0013t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0013t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0016t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0016t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0019t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0019t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0026t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0027t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0001c0033t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0006g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0012g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0015g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0021g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0021g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0023g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0023g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0035g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0036g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0002c0002t0043g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0008g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0018g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0018g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0026g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0003c0003t0026g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0010g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0004t0039g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0004c0032t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0011g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0013g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0017g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0019g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0019g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0019g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0024g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0038g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0041g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0005c0005t0046g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0009g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0006c0006t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0007c0008t0032g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0008c0009t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0009c0010t0016g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0009c0010t0016g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0009c0010t0016g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0009c0010t0016g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0009c0010t0042g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0010c0011t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0010c0011t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0010c0011t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0010c0011t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0011c0012t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0011c0012t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0011c0012t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0012c0014t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0012c0014t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0012c0014t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0013c0017t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0013c0017t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0014c0015t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0014c0015t0018g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0015c0018t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0015c0018t0017g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0016c0030t0016g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0017c0031t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0018c0023t0045g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0019c0034t0020g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0020c0029t0031g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0021c0025t0021g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0022c0035t0017g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0023c0024t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0024c0022t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0025c0028t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0026c0020t0010g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
a0027c0021t0037g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0012 | g0211 | EUR | GBR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00140 | hp2 | a0006 | c0006 | t0001 | g0295 | EUR | GBR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0190 | EUR | FIN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00323 | hp2 | a0001 | c0013 | t0002 | g0072 | EUR | FIN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00408 | hp2 | a0001 | c0001 | t0012 | g0214 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00423 | hp1 | a0003 | c0003 | t0008 | g0036 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00438 | hp2 | a0001 | c0001 | t0013 | g0324 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00558 | hp1 | a0004 | c0004 | t0004 | g0260 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00597 | hp2 | a0004 | c0004 | t0003 | g0271 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00609 | hp2 | a0003 | c0003 | t0005 | g0048 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00621 | hp1 | a0003 | c0003 | t0008 | g0034 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00673 | hp2 | a0002 | c0002 | t0006 | g0366 | EAS | CHS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0361 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00735 | hp2 | a0001 | c0001 | t0028 | g0237 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00738 | hp1 | a0016 | c0030 | t0016 | g0305 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01069 | hp1 | a0001 | c0026 | t0002 | g0096 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0356 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0303 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01074 | hp2 | a0002 | c0002 | t0006 | g0005 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01081 | hp1 | a0006 | c0006 | t0001 | g0297 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01081 | hp2 | a0002 | c0002 | t0006 | g0005 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01109 | hp1 | a0006 | c0006 | t0001 | g0298 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01109 | hp2 | a0005 | c0005 | t0011 | g0342 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0362 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0360 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01175 | hp1 | a0004 | c0004 | t0003 | g0283 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01175 | hp2 | a0006 | c0006 | t0009 | g0158 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01255 | hp1 | a0005 | c0005 | t0046 | g0300 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01255 | hp2 | a0002 | c0002 | t0009 | g0132 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0353 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01358 | hp1 | a0006 | c0006 | t0001 | g0299 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01515 | hp1 | a0001 | c0007 | t0002 | g0006 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01515 | hp2 | a0002 | c0002 | t0035 | g0129 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0131 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01517 | hp2 | a0001 | c0007 | t0002 | g0006 | EUR | IBS | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01884 | hp1 | a0005 | c0005 | t0006 | g0248 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01884 | hp2 | a0011 | c0012 | t0014 | g0226 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0372 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0354 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01928 | hp2 | a0004 | c0004 | t0003 | g0253 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0359 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01934 | hp2 | a0001 | c0007 | t0002 | g0100 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0355 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01975 | hp2 | a0009 | c0010 | t0016 | g0344 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01978 | hp2 | a0004 | c0004 | t0003 | g0277 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0357 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02004 | hp1 | a0004 | c0004 | t0003 | g0266 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02004 | hp2 | a0006 | c0006 | t0001 | g0163 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02015 | hp1 | a0003 | c0003 | t0005 | g0026 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02027 | hp1 | a0003 | c0003 | t0008 | g0056 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02040 | hp2 | a0003 | c0003 | t0005 | g0055 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02055 | hp1 | a0001 | c0001 | t0022 | g0239 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0143 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02056 | hp1 | a0003 | c0003 | t0008 | g0052 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02056 | hp2 | a0002 | c0002 | t0009 | g0215 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0339 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02074 | hp2 | a0003 | c0003 | t0005 | g0019 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02080 | hp2 | a0003 | c0003 | t0008 | g0047 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02083 | hp2 | a0017 | c0031 | t0005 | g0038 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02129 | hp1 | a0002 | c0002 | t0006 | g0080 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02129 | hp2 | a0004 | c0004 | t0003 | g0264 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02148 | hp1 | a0001 | c0007 | t0002 | g0103 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02148 | hp2 | a0004 | c0004 | t0010 | g0290 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02155 | hp1 | a0004 | c0004 | t0006 | g0276 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02155 | hp2 | a0003 | c0003 | t0005 | g0027 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02165 | hp1 | a0004 | c0004 | t0003 | g0127 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02165 | hp2 | a0002 | c0002 | t0012 | g0173 | EAS | CDX | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02257 | hp1 | a0013 | c0017 | t0007 | g0136 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0144 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0142 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02258 | hp2 | a0006 | c0006 | t0001 | g0162 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02280 | hp1 | a0002 | c0002 | t0023 | g0220 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02280 | hp2 | a0001 | c0001 | t0022 | g0236 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0358 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02293 | hp2 | a0002 | c0002 | t0009 | g0172 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PEL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02523 | hp1 | a0014 | c0015 | t0005 | g0365 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02572 | hp1 | a0001 | c0001 | t0034 | g0011 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02572 | hp2 | a0005 | c0005 | t0024 | g0001 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02602 | hp1 | a0006 | c0006 | t0009 | g0159 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02615 | hp1 | a0001 | c0001 | t0033 | g0231 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02615 | hp2 | a0001 | c0019 | t0017 | g0141 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0146 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02622 | hp2 | a0012 | c0014 | t0007 | g0135 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02630 | hp1 | a0001 | c0019 | t0007 | g0140 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0229 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0118 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02647 | hp2 | a0005 | c0005 | t0007 | g0241 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02723 | hp1 | a0001 | c0001 | t0020 | g0230 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02723 | hp2 | a0005 | c0005 | t0007 | g0278 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02735 | hp1 | a0003 | c0003 | t0005 | g0025 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02735 | hp2 | a0006 | c0006 | t0001 | g0294 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02738 | hp1 | a0003 | c0003 | t0005 | g0057 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0105 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02809 | hp1 | a0020 | c0029 | t0031 | g0234 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02809 | hp2 | a0015 | c0018 | t0017 | g0134 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02886 | hp1 | a0001 | c0001 | t0015 | g0373 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02886 | hp2 | a0005 | c0005 | t0017 | g0244 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02895 | hp1 | a0009 | c0010 | t0016 | g0346 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02896 | hp2 | a0009 | c0010 | t0016 | g0345 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02922 | hp1 | a0005 | c0005 | t0006 | g0245 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02922 | hp2 | a0012 | c0014 | t0007 | g0138 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02965 | hp1 | a0015 | c0018 | t0017 | g0063 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02965 | hp2 | a0001 | c0001 | t0020 | g0011 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02970 | hp1 | a0021 | c0025 | t0021 | g0279 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02970 | hp2 | a0005 | c0005 | t0019 | g0246 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02976 | hp1 | a0022 | c0035 | t0017 | g0126 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02976 | hp2 | a0005 | c0005 | t0019 | g0243 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03017 | hp2 | a0006 | c0006 | t0001 | g0161 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03098 | hp2 | a0005 | c0005 | t0041 | g0251 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03130 | hp1 | a0023 | c0024 | t0007 | g0280 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03130 | hp2 | a0001 | c0001 | t0015 | g0371 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03139 | hp2 | a0001 | c0001 | t0040 | g0122 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0232 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03209 | hp1 | a0011 | c0012 | t0014 | g0227 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0119 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0145 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03239 | hp2 | a0003 | c0003 | t0005 | g0028 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03453 | hp1 | a0001 | c0001 | t0029 | g0238 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03486 | hp2 | a0009 | c0010 | t0042 | g0343 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03490 | hp2 | a0003 | c0003 | t0008 | g0002 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03491 | hp1 | a0006 | c0006 | t0001 | g0009 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03491 | hp2 | a0001 | c0007 | t0002 | g0102 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03492 | hp1 | a0003 | c0003 | t0005 | g0002 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03492 | hp2 | a0006 | c0006 | t0001 | g0009 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03516 | hp1 | a0024 | c0022 | t0006 | g0286 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03516 | hp2 | a0001 | c0001 | t0018 | g0233 | AFR | ESN | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03669 | hp2 | a0004 | c0004 | t0003 | g0284 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03704 | hp1 | a0002 | c0002 | t0043 | g0350 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0165 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03710 | hp1 | a0004 | c0004 | t0003 | g0250 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03710 | hp2 | a0001 | c0013 | t0006 | g0073 | SAS | PJL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03831 | hp1 | a0003 | c0003 | t0008 | g0031 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03834 | hp1 | a0002 | c0002 | t0036 | g0221 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03942 | hp1 | a0003 | c0003 | t0018 | g0168 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0306 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04115 | hp1 | a0002 | c0002 | t0009 | g0186 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04115 | hp2 | a0004 | c0004 | t0010 | g0272 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04184 | hp2 | a0001 | c0007 | t0002 | g0117 | SAS | BEB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04199 | hp1 | a0001 | c0007 | t0002 | g0116 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04199 | hp2 | a0006 | c0006 | t0001 | g0217 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04204 | hp1 | a0003 | c0003 | t0005 | g0050 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG04204 | hp2 | a0002 | c0002 | t0006 | g0351 | SAS | STU | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18522 | hp1 | a0002 | c0002 | t0023 | g0222 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18522 | hp2 | a0001 | c0001 | t0014 | g0235 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18612 | hp1 | a0003 | c0003 | t0005 | g0035 | EAS | CHB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18612 | hp2 | a0001 | c0001 | t0015 | g0191 | EAS | CHB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18906 | hp1 | a0005 | c0005 | t0019 | g0012 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18939 | hp1 | a0003 | c0003 | t0005 | g0039 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18939 | hp2 | a0007 | c0008 | t0003 | g0317 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18941 | hp1 | a0002 | c0002 | t0021 | g0341 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18942 | hp2 | a0004 | c0004 | t0004 | g0273 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18945 | hp1 | a0003 | c0003 | t0008 | g0042 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18946 | hp1 | a0008 | c0009 | t0001 | g0185 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18946 | hp2 | a0001 | c0001 | t0027 | g0068 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18947 | hp1 | a0003 | c0003 | t0008 | g0059 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18947 | hp2 | a0007 | c0008 | t0003 | g0318 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18949 | hp1 | a0004 | c0004 | t0010 | g0265 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18949 | hp2 | a0002 | c0002 | t0006 | g0349 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18950 | hp1 | a0008 | c0009 | t0001 | g0184 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18951 | hp1 | a0003 | c0003 | t0005 | g0041 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18951 | hp2 | a0001 | c0001 | t0012 | g0212 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18953 | hp1 | a0003 | c0003 | t0008 | g0368 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18953 | hp2 | a0010 | c0011 | t0001 | g0179 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18954 | hp1 | a0004 | c0004 | t0003 | g0313 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18956 | hp1 | a0004 | c0004 | t0010 | g0062 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18956 | hp2 | a0010 | c0011 | t0001 | g0199 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18959 | hp1 | a0002 | c0002 | t0006 | g0335 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18960 | hp1 | a0001 | c0027 | t0004 | g0326 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18962 | hp1 | a0010 | c0011 | t0001 | g0200 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18962 | hp2 | a0003 | c0003 | t0005 | g0030 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18963 | hp1 | a0002 | c0002 | t0006 | g0367 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18963 | hp2 | a0001 | c0001 | t0006 | g0311 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18964 | hp2 | a0004 | c0004 | t0003 | g0267 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18965 | hp1 | a0004 | c0004 | t0003 | g0281 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18965 | hp2 | a0003 | c0003 | t0005 | g0032 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18966 | hp1 | a0004 | c0004 | t0003 | g0268 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18967 | hp1 | a0002 | c0002 | t0009 | g0164 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18967 | hp2 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18968 | hp1 | a0001 | c0016 | t0006 | g0029 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18970 | hp2 | a0008 | c0009 | t0001 | g0060 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18971 | hp2 | a0001 | c0016 | t0002 | g0051 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18973 | hp1 | a0004 | c0004 | t0003 | g0270 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18973 | hp2 | a0002 | c0002 | t0009 | g0150 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18974 | hp1 | a0004 | c0004 | t0003 | g0289 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18974 | hp2 | a0001 | c0033 | t0004 | g0315 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18978 | hp1 | a0003 | c0003 | t0008 | g0058 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18978 | hp2 | a0004 | c0004 | t0003 | g0302 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18979 | hp1 | a0004 | c0004 | t0003 | g0269 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18979 | hp2 | a0003 | c0003 | t0008 | g0046 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18980 | hp1 | a0007 | c0008 | t0003 | g0319 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18981 | hp1 | a0004 | c0004 | t0003 | g0259 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18983 | hp1 | a0004 | c0004 | t0003 | g0257 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18984 | hp1 | a0001 | c0001 | t0015 | g0175 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18985 | hp1 | a0004 | c0004 | t0010 | g0255 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18985 | hp2 | a0001 | c0001 | t0013 | g0340 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18988 | hp2 | a0002 | c0002 | t0015 | g0153 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18989 | hp1 | a0001 | c0001 | t0030 | g0196 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18989 | hp2 | a0004 | c0004 | t0010 | g0261 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18991 | hp1 | a0002 | c0002 | t0009 | g0205 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18991 | hp2 | a0004 | c0004 | t0003 | g0252 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18994 | hp1 | a0004 | c0004 | t0003 | g0013 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18994 | hp2 | a0003 | c0003 | t0026 | g0021 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18995 | hp2 | a0003 | c0003 | t0008 | g0033 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18998 | hp1 | a0003 | c0003 | t0005 | g0044 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA18999 | hp2 | a0003 | c0003 | t0008 | g0045 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19000 | hp1 | a0026 | c0020 | t0010 | g0288 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19001 | hp1 | a0001 | c0001 | t0025 | g0098 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19002 | hp2 | a0003 | c0003 | t0026 | g0020 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19004 | hp2 | a0003 | c0003 | t0005 | g0040 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19005 | hp1 | a0004 | c0004 | t0003 | g0242 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19006 | hp1 | a0004 | c0004 | t0010 | g0287 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19007 | hp1 | a0004 | c0004 | t0003 | g0254 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19009 | hp1 | a0004 | c0004 | t0003 | g0258 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19009 | hp2 | a0003 | c0003 | t0005 | g0003 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19012 | hp2 | a0007 | c0008 | t0006 | g0086 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19030 | hp1 | a0005 | c0005 | t0007 | g0282 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19043 | hp1 | a0012 | c0014 | t0007 | g0139 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19043 | hp2 | a0005 | c0005 | t0038 | g0274 | AFR | LWK | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19054 | hp1 | a0014 | c0015 | t0018 | g0170 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19054 | hp2 | a0004 | c0004 | t0003 | g0013 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19058 | hp1 | a0003 | c0003 | t0005 | g0022 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19058 | hp2 | a0008 | c0009 | t0001 | g0187 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19060 | hp1 | a0007 | c0008 | t0032 | g0195 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19062 | hp1 | a0003 | c0003 | t0005 | g0023 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19063 | hp2 | a0001 | c0001 | t0027 | g0087 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19064 | hp1 | a0003 | c0003 | t0005 | g0043 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19065 | hp1 | a0003 | c0003 | t0005 | g0054 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19065 | hp2 | a0001 | c0001 | t0025 | g0097 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19066 | hp1 | a0005 | c0005 | t0013 | g0256 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19066 | hp2 | a0003 | c0003 | t0005 | g0003 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19070 | hp1 | a0003 | c0003 | t0018 | g0225 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19074 | hp1 | a0005 | c0005 | t0004 | g0301 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19074 | hp2 | a0004 | c0004 | t0003 | g0263 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19076 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19076 | hp2 | a0003 | c0003 | t0005 | g0049 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19077 | hp1 | a0004 | c0004 | t0003 | g0374 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0337 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19078 | hp1 | a0002 | c0002 | t0021 | g0314 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19078 | hp2 | a0007 | c0008 | t0003 | g0363 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0364 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19080 | hp2 | a0003 | c0003 | t0005 | g0037 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19081 | hp2 | a0008 | c0009 | t0001 | g0188 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19082 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19082 | hp2 | a0007 | c0008 | t0003 | g0369 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19084 | hp1 | a0008 | c0009 | t0009 | g0183 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19087 | hp1 | a0001 | c0001 | t0044 | g0081 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19087 | hp2 | a0008 | c0009 | t0001 | g0061 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19090 | hp1 | a0001 | c0001 | t0013 | g0348 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19090 | hp2 | a0010 | c0011 | t0001 | g0219 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19091 | hp2 | a0003 | c0003 | t0005 | g0053 | EAS | JPT | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19240 | hp1 | a0005 | c0005 | t0019 | g0012 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA19240 | hp2 | a0005 | c0005 | t0024 | g0001 | AFR | YRI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20129 | hp1 | a0009 | c0010 | t0016 | g0352 | AFR | ASW | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ASW | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20805 | hp1 | a0004 | c0032 | t0003 | g0262 | EUR | TSI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0216 | EUR | TSI | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20905 | hp1 | a0001 | c0013 | t0002 | g0074 | SAS | GIH | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20905 | hp2 | a0004 | c0004 | t0039 | g0240 | SAS | GIH | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG01123 | hp2 | a0001 | c0007 | t0002 | g0101 | AMR | CLM | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02486 | hp1 | a0005 | c0005 | t0007 | g0275 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02486 | hp2 | a0013 | c0017 | t0007 | g0137 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02559 | hp1 | a0018 | c0023 | t0045 | g0247 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG02559 | hp2 | a0019 | c0034 | t0020 | g0370 | AFR | ACB | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03471 | hp1 | a0005 | c0005 | t0007 | g0001 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG03471 | hp2 | a0011 | c0012 | t0014 | g0228 | AFR | MSL | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0312 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
HG06807 | hp2 | a0025 | c0028 | t0001 | g0016 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20300 | hp1 | a0004 | c0004 | t0003 | g0285 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
NA20300 | hp2 | a0002 | c0002 | t0009 | g0208 | AFR | USA | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
homoSapiens | chm13v2 | a0027 | c0021 | t0037 | g0296 | REF | REF | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
homoSapiens | grch38p0 | a0006 | c0006 | t0001 | g0204 | REF | REF | EGF_chr4_109907883_110018766 | EGF | chr4 | 109907883 | 110018766 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:109913381 | A | C | 1 | a0008 | 7 | NA18946.hp1 NA18950.hp1 NA18970.hp2 others(4): Show |
missense_variant | MODERATE | c.46A>C | p.Ser16Arg | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 499/6388 | 46/3624 | 16/1207 | chr4 | 109913381 | |||
chr4:109913435 | G | A | 1 | a0026 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 553/6388 | 100/3624 | 34/1207 | chr4 | 109913435 | |||
chr4:109943377 | C | T | 3 | a0012 a0013 a0015 |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.451C>T | p.His151Tyr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/24 | 904/6388 | 451/3624 | 151/1207 | chr4 | 109943377 | |||
chr4:109943888 | G | C | 3 | a0012 a0013 a0015 |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.556G>C | p.Asp186His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/24 | 1009/6388 | 556/3624 | 186/1207 | chr4 | 109943888 | |||
chr4:109945104 | G | C | 1 | a0011 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.769G>C | p.Asp257His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/24 | 1222/6388 | 769/3624 | 257/1207 | chr4 | 109945104 | |||
chr4:109945210 | T | A | 1 | a0019 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.875T>A | p.Leu292His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/24 | 1328/6388 | 875/3624 | 292/1207 | chr4 | 109945210 | |||
chr4:109961965 | G | A | 8 | a0004 a0005 a0009 others(5): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
missense_variant | MODERATE | c.1292G>A | p.Arg431Lys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/24 | 1745/6388 | 1292/3624 | 431/1207 | chr4 | 109961965 | |||
chr4:109963227 | C | A | 1 | a0024 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1367C>A | p.Pro456Gln | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/24 | 1820/6388 | 1367/3624 | 456/1207 | chr4 | 109963227 | |||
chr4:109976096 | C | G | 1 | a0011 | 3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.1914C>G | p.Ser638Arg | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/24 | 2367/6388 | 1914/3624 | 638/1207 | chr4 | 109976096 | |||
chr4:109976211 | C | T | 1 | a0017 | 1 | HG02083.hp2 | stop_gained | HIGH | c.2029C>T | p.Arg677* | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/24 | 2482/6388 | 2029/3624 | 677/1207 | chr4 | 109976211 | |||
chr4:109980042 | G | A | 19 | a0001 a0003 a0004 others(16): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
missense_variant | MODERATE | c.2124G>A | p.Met708Ile | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/24 | 2577/6388 | 2124/3624 | 708/1207 | chr4 | 109980042 | |||
chr4:109980955 | A | T | 3 | a0004 a0007 a0026 |
48 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(45): Show |
missense_variant | MODERATE | c.2351A>T | p.Asp784Val | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/24 | 2804/6388 | 2351/3624 | 784/1207 | chr4 | 109980955 | |||
chr4:109987777 | T | C | 4 | a0015 a0016 a0019 others(1): Show |
5 | HG00738.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.2525T>C | p.Met842Thr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/24 | 2978/6388 | 2525/3624 | 842/1207 | chr4 | 109987777 | |||
chr4:109988649 | G | A | 1 | a0025 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2674G>A | p.Glu892Lys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/24 | 3127/6388 | 2674/3624 | 892/1207 | chr4 | 109988649 | |||
chr4:109993271 | A | T | 25 | a0001 a0002 a0003 others(22): Show |
373 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(370): Show |
missense_variant | MODERATE | c.2759A>T | p.Glu920Val | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/24 | 3212/6388 | 2759/3624 | 920/1207 | chr4 | 109993271 | |||
chr4:109999791 | G | A | 1 | a0010 | 4 | NA18953.hp2 NA18956.hp2 NA18962.hp1 others(1): Show |
missense_variant | MODERATE | c.3118G>A | p.Val1040Met | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/24 | 3571/6388 | 3118/3624 | 1040/1207 | chr4 | 109999791 | |||
chr4:109999800 | C | T | 2 | a0009 a0016 |
6 | HG00738.hp1 HG01975.hp2 HG02895.hp1 others(3): Show |
missense_variant | MODERATE | c.3127C>T | p.Leu1043Phe | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/24 | 3580/6388 | 3127/3624 | 1043/1207 | chr4 | 109999800 | |||
chr4:110004582 | C | G | 2 | a0018 a0020 |
2 | HG02559.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.3251C>G | p.Ala1084Gly | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/24 | 3704/6388 | 3251/3624 | 1084/1207 | chr4 | 110004582 | |||
chr4:110011233 | G | GC | 3 | a0003 a0014 a0017 |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
frameshift_variant | HIGH | c.3406dupC | p.Gln1136fs | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 3860/6388 | 3407/3624 | 1136/1207 | INFO_REALIGN_3_PRIME | chr4 | 110011233 | ||
chr4:110011352 | C | A | 2 | a0013 a0023 |
3 | HG02257.hp1 HG02486.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.3521C>A | p.Thr1174Asn | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 3974/6388 | 3521/3624 | 1174/1207 | chr4 | 110011352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:109941082 | C | T | 3 | a0001c0019 a0019c0034 a0022c0035 |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.264C>T | p.Ile88Ile | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/24 | 717/6388 | 264/3624 | 88/1207 | chr4 | 109941082 | |||
chr4:109943379 | C | T | 1 | a0001c0033 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.453C>T | p.His151His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/24 | 906/6388 | 453/3624 | 151/1207 | chr4 | 109943379 | |||
chr4:109960895 | T | C | 1 | a0001c0013 | 3 | HG00323.hp2 HG03710.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.1095T>C | p.His365His | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/24 | 1548/6388 | 1095/3624 | 365/1207 | chr4 | 109960895 | |||
chr4:109960928 | A | T | 1 | a0004c0032 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1128A>T | p.Gly376Gly | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/24 | 1581/6388 | 1128/3624 | 376/1207 | chr4 | 109960928 | |||
chr4:109968997 | G | A | 1 | a0001c0026 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.1602G>A | p.Lys534Lys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/24 | 2055/6388 | 1602/3624 | 534/1207 | chr4 | 109968997 | |||
chr4:109969105 | T | C | 1 | a0001c0027 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.1710T>C | p.Tyr570Tyr | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/24 | 2163/6388 | 1710/3624 | 570/1207 | chr4 | 109969105 | |||
chr4:109976159 | C | T | 1 | a0001c0007 | 8 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
synonymous_variant | LOW | c.1977C>T | p.Cys659Cys | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/24 | 2430/6388 | 1977/3624 | 659/1207 | chr4 | 109976159 | |||
chr4:109979991 | A | G | 7 | a0001c0016 a0003c0003 a0015c0018 others(4): Show |
52 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
synonymous_variant | LOW | c.2073A>G | p.Ala691Ala | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/24 | 2526/6388 | 2073/3624 | 691/1207 | chr4 | 109979991 | |||
chr4:109980902 | G | A | 1 | a0015c0018 | 2 | HG02809.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.2298G>A | p.Ser766Ser | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/24 | 2751/6388 | 2298/3624 | 766/1207 | chr4 | 109980902 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:109912912 | G | A | 3 | a0001c0001t0022 a0001c0001t0028 a0001c0001t0029 |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-424G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 424 | chr4 | 109912912 | ||||||
chr4:109912954 | A | G | 64 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(61): Show |
267 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(264): Show |
5_prime_UTR_variant | MODIFIER | c.-382A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 382 | chr4 | 109912954 | ||||||
chr4:109912994 | C | T | 3 | a0005c0005t0019 a0005c0005t0046 a0018c0023t0045 |
6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-342C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 342 | chr4 | 109912994 | ||||||
chr4:109913258 | A | G | 2 | a0001c0001t0027 a0001c0001t0044 |
3 | NA18946.hp2 NA19063.hp2 NA19087.hp1 |
5_prime_UTR_variant | MODIFIER | c.-78A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/24 | 78 | chr4 | 109913258 | ||||||
chr4:110011612 | G | A | 1 | a0001c0001t0030 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 157 | chr4 | 110011612 | ||||||
chr4:110011848 | T | C | 11 | a0001c0001t0003 a0004c0004t0003 a0004c0004t0010 others(8): Show |
50 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*393T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 393 | chr4 | 110011848 | ||||||
chr4:110011938 | C | T | 4 | a0001c0019t0017 a0005c0005t0017 a0015c0018t0017 others(1): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 483 | chr4 | 110011938 | ||||||
chr4:110012367 | G | GT | 6 | a0002c0002t0009 a0002c0002t0021 a0003c0003t0008 others(3): Show |
28 | HG00423.hp1 HG00621.hp1 HG01175.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*926dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 927 | INFO_REALIGN_3_PRIME | chr4 | 110012367 | |||||
chr4:110012367 | GT | G | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
193 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*926delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 926 | INFO_REALIGN_3_PRIME | chr4 | 110012367 | |||||
chr4:110012367 | GTT | G | 6 | a0001c0001t0028 a0001c0001t0033 a0001c0019t0017 others(3): Show |
7 | HG00735.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*926delTT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 925 | INFO_REALIGN_3_PRIME | chr4 | 110012367 | |||||
chr4:110012384 | G | A | 2 | a0005c0005t0024 a0005c0005t0041 |
3 | HG02572.hp2 HG03098.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 929 | chr4 | 110012384 | ||||||
chr4:110012624 | C | T | 1 | a0002c0002t0043 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1169 | chr4 | 110012624 | ||||||
chr4:110012677 | A | G | 13 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0015 others(10): Show |
55 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1222A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1222 | chr4 | 110012677 | ||||||
chr4:110012699 | T | C | 58 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(55): Show |
207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1244T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1244 | chr4 | 110012699 | ||||||
chr4:110012721 | T | A | 2 | a0001c0001t0011 a0005c0005t0011 |
8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1266T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1266 | chr4 | 110012721 | ||||||
chr4:110012738 | C | T | 1 | a0003c0003t0026 | 2 | NA18994.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1283C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1283 | chr4 | 110012738 | ||||||
chr4:110012890 | T | C | 2 | a0018c0023t0045 a0020c0029t0031 |
2 | HG02559.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1435T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1435 | chr4 | 110012890 | ||||||
chr4:110013029 | G | A | 1 | a0002c0002t0023 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1574G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1574 | chr4 | 110013029 | ||||||
chr4:110013043 | G | C | 3 | a0009c0010t0016 a0009c0010t0042 a0016c0030t0016 |
6 | HG00738.hp1 HG01975.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1588G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1588 | chr4 | 110013043 | ||||||
chr4:110013214 | T | G | 1 | a0005c0005t0038 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1759 | chr4 | 110013214 | ||||||
chr4:110013278 | C | A | 4 | a0001c0001t0020 a0001c0001t0034 a0001c0001t0040 others(1): Show |
5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1823C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1823 | chr4 | 110013278 | ||||||
chr4:110013284 | T | C | 3 | a0001c0001t0022 a0001c0001t0029 a0005c0005t0019 |
7 | HG02055.hp1 HG02280.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1829T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 1829 | chr4 | 110013284 | ||||||
chr4:110013488 | T | A | 1 | a0004c0004t0039 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2033T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2033 | chr4 | 110013488 | ||||||
chr4:110013496 | G | C | 8 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0028 others(5): Show |
15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2041 | chr4 | 110013496 | ||||||
chr4:110013614 | T | C | 1 | a0002c0002t0035 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2159 | chr4 | 110013614 | ||||||
chr4:110013649 | T | C | 8 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0028 others(5): Show |
15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2194T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2194 | chr4 | 110013649 | ||||||
chr4:110013650 | C | G | 8 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0028 others(5): Show |
15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2195C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2195 | chr4 | 110013650 | ||||||
chr4:110013691 | T | A | 1 | a0002c0002t0036 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2236T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2236 | chr4 | 110013691 | ||||||
chr4:110013729 | C | T | 8 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0028 others(5): Show |
15 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2274C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2274 | chr4 | 110013729 | ||||||
chr4:110013731 | C | A | 1 | a0001c0001t0025 | 2 | NA19001.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 24/24 | 2276 | chr4 | 110013731 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:109913475 | A | G | 1 | a0004c0004t0003g0374 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.127+13A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913475 | |||||||
chr4:109913491 | G | T | 4 | a0001c0001t0012g0372 a0001c0001t0015g0371 a0001c0001t0015g0373 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+29G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913491 | |||||||
chr4:109913560 | G | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0017 others(2): Show |
5 | HG02818.hp1 HG03225.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+98G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913560 | |||||||
chr4:109913569 | T | C | 44 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+107T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913569 | |||||||
chr4:109913761 | G | A | 2 | a0008c0009t0001g0060 a0008c0009t0001g0061 |
2 | NA18970.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.127+299G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913761 | |||||||
chr4:109913764 | A | G | 58 | a0001c0001t0004g0316 a0001c0001t0004g0320 a0001c0001t0004g0321 others(55): Show |
58 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.127+302A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913764 | |||||||
chr4:109913781 | T | TG | 44 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+320dupG | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109913781 | ||||||
chr4:109913898 | A | T | 58 | a0001c0001t0004g0316 a0001c0001t0004g0320 a0001c0001t0004g0321 others(55): Show |
58 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.127+436A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109913898 | |||||||
chr4:109914282 | T | TG | 44 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+820_127+821ins others(1): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914282 | |||||||
chr4:109914288 | C | T | 5 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0310 others(2): Show |
5 | NA18963.hp2 NA18967.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+826C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914288 | |||||||
chr4:109914354 | T | C | 1 | a0004c0004t0010g0062 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.127+892T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914354 | |||||||
chr4:109914382 | A | G | 1 | a0002c0002t0001g0306 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.127+920A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914382 | |||||||
chr4:109914587 | G | C | 44 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.127+1125G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914587 | |||||||
chr4:109914687 | T | A | 1 | a0015c0018t0017g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127+1225T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914687 | |||||||
chr4:109914829 | A | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+1367A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914829 | |||||||
chr4:109914874 | A | G | 2 | a0002c0002t0001g0303 a0002c0002t0001g0304 |
2 | HG00733.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.127+1412A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914874 | |||||||
chr4:109914892 | G | A | 62 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(59): Show |
65 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.127+1430G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914892 | |||||||
chr4:109914925 | G | T | 1 | a0004c0004t0003g0302 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127+1463G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914925 | |||||||
chr4:109914926 | T | G | 1 | a0004c0004t0003g0302 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127+1464T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109914926 | |||||||
chr4:109915099 | G | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+1637G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915099 | |||||||
chr4:109915315 | T | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+1853T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915315 | |||||||
chr4:109915355 | C | A | 1 | a0004c0004t0003g0302 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127+1893C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915355 | |||||||
chr4:109915408 | G | A | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+1946G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915408 | |||||||
chr4:109915434 | A | T | 1 | a0005c0005t0004g0301 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.127+1972A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915434 | |||||||
chr4:109915444 | A | G | 1 | a0007c0008t0003g0369 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.127+1982A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915444 | |||||||
chr4:109915471 | C | T | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127+2009C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915471 | |||||||
chr4:109915606 | C | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+2144C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915606 | |||||||
chr4:109915733 | C | T | 5 | a0006c0006t0001g0294 a0006c0006t0001g0295 a0006c0006t0001g0297 others(2): Show |
5 | HG00140.hp2 HG01081.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2271C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915733 | |||||||
chr4:109915849 | G | A | 1 | a0004c0004t0003g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127+2387G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109915849 | |||||||
chr4:109916131 | C | T | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+2669C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916131 | |||||||
chr4:109916226 | A | T | 45 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.127+2764A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916226 | |||||||
chr4:109916333 | C | T | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+2871C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916333 | |||||||
chr4:109916364 | T | C | 6 | a0002c0002t0001g0128 a0002c0002t0001g0130 a0002c0002t0001g0131 others(3): Show |
6 | HG00738.hp2 HG01192.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+2902T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916364 | |||||||
chr4:109916417 | C | A | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+2955C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916417 | |||||||
chr4:109916425 | TGC | T | 5 | a0001c0001t0004g0364 a0002c0002t0006g0366 a0002c0002t0006g0367 others(2): Show |
5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2964_127+2965d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916425 | |||||||
chr4:109916430 | C | CCTGGATT others(14): Show |
5 | a0001c0001t0004g0364 a0002c0002t0006g0366 a0002c0002t0006g0367 others(2): Show |
5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2968_127+2969i others(23): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916430 | |||||||
chr4:109916431 | T | A | 5 | a0001c0001t0004g0364 a0002c0002t0006g0366 a0002c0002t0006g0367 others(2): Show |
5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2969T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916431 | |||||||
chr4:109916452 | T | C | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127+2990T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916452 | |||||||
chr4:109916511 | G | A | 214 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(211): Show |
221 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.127+3049G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916511 | |||||||
chr4:109916574 | C | T | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127+3112C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916574 | |||||||
chr4:109916623 | T | A | 1 | a0004c0004t0039g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127+3161T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916623 | |||||||
chr4:109916635 | T | C | 1 | a0005c0005t0007g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127+3173T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916635 | |||||||
chr4:109916729 | G | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+3267G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916729 | |||||||
chr4:109916747 | G | GT | 276 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(273): Show |
284 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.127+3289dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109916747 | ||||||
chr4:109916784 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127+3322G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916784 | |||||||
chr4:109916839 | A | G | 10 | a0001c0001t0004g0353 a0001c0001t0004g0355 a0001c0001t0004g0356 others(7): Show |
10 | HG00733.hp2 HG01070.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.127+3377A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916839 | |||||||
chr4:109916853 | T | C | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127+3391T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916853 | |||||||
chr4:109916970 | G | A | 260 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(257): Show |
268 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.127+3508G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109916970 | |||||||
chr4:109917133 | G | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG00735.hp1 HG01358.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.127+3671G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917133 | |||||||
chr4:109917431 | A | G | 1 | a0001c0007t0002g0117 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127+3969A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917431 | |||||||
chr4:109917706 | C | T | 259 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(256): Show |
267 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.127+4244C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917706 | |||||||
chr4:109917779 | C | T | 3 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 |
3 | HG02717.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127+4317C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917779 | |||||||
chr4:109917780 | C | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+4318C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917780 | |||||||
chr4:109917794 | A | AT | 3 | a0001c0001t0012g0372 a0001c0001t0015g0371 a0001c0001t0015g0373 |
3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+4337dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109917794 | ||||||
chr4:109917799 | T | C | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+4337T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917799 | |||||||
chr4:109917835 | G | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.127+4373G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109917835 | |||||||
chr4:109918255 | G | GT | 208 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(205): Show |
215 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.127+4809dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109918255 | ||||||
chr4:109918273 | A | T | 5 | a0001c0001t0004g0364 a0002c0002t0006g0366 a0002c0002t0006g0367 others(2): Show |
5 | HG00673.hp2 HG02523.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+4811A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918273 | |||||||
chr4:109918299 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.127+4837T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918299 | |||||||
chr4:109918345 | C | T | 55 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(52): Show |
57 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.127+4883C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918345 | |||||||
chr4:109918370 | G | A | 1 | a0004c0004t0003g0313 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.127+4908G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918370 | |||||||
chr4:109918514 | C | T | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+5052C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918514 | |||||||
chr4:109918671 | C | T | 3 | a0006c0006t0001g0297 a0006c0006t0001g0298 a0006c0006t0001g0299 |
3 | HG01081.hp1 HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.127+5209C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918671 | |||||||
chr4:109918676 | C | A | 1 | a0002c0002t0009g0150 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.127+5214C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918676 | |||||||
chr4:109918798 | C | T | 71 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(68): Show |
75 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.127+5336C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918798 | |||||||
chr4:109918832 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+5370T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918832 | |||||||
chr4:109918872 | G | A | 6 | a0001c0001t0002g0071 a0001c0001t0002g0075 a0001c0001t0002g0076 others(3): Show |
6 | HG00323.hp2 HG02300.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+5410G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918872 | |||||||
chr4:109918923 | G | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0151 a0002c0002t0001g0152 others(5): Show |
9 | NA18941.hp2 NA18957.hp1 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+5461G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109918923 | |||||||
chr4:109919250 | G | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+5788G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919250 | |||||||
chr4:109919267 | T | C | 3 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 |
4 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5805T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919267 | |||||||
chr4:109919287 | G | GTC | 26 | a0001c0001t0002g0070 a0001c0001t0002g0104 a0001c0001t0002g0109 others(23): Show |
26 | HG00733.hp1 HG01169.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.127+5878_127+5879d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | G | GTCTC | 19 | a0001c0001t0002g0106 a0001c0001t0002g0108 a0001c0001t0002g0125 others(16): Show |
19 | HG00408.hp2 HG01070.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+5876_127+5879d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | G | GTCTCTC | 5 | a0001c0001t0002g0112 a0001c0001t0033g0231 a0002c0002t0001g0193 others(2): Show |
5 | HG00438.hp1 HG00597.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+5874_127+5879d others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | G | GTCTCTCT others(1): Show |
4 | a0001c0001t0002g0307 a0002c0002t0001g0169 a0002c0002t0001g0213 others(1): Show |
4 | NA19006.hp2 NA19086.hp2 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+5872_127+5879d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | G | GTCTCTCT others(3): Show |
1 | a0002c0002t0009g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.127+5870_127+5879d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | G | GTCTCTCT others(13): Show |
1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+5860_127+5879d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | G | GTCTCTGT others(3): Show |
1 | a0001c0001t0015g0371 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127+5830_127+5831i others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTC | G | 37 | a0001c0001t0002g0004 a0001c0001t0002g0076 a0001c0001t0002g0089 others(34): Show |
37 | HG00140.hp2 HG00438.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.127+5878_127+5879d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTC | G | 39 | a0001c0001t0002g0004 a0001c0001t0002g0067 a0001c0001t0002g0083 others(36): Show |
40 | HG00408.hp1 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.127+5876_127+5879d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTC | G | 33 | a0001c0001t0002g0069 a0001c0001t0002g0071 a0001c0001t0002g0075 others(30): Show |
34 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.127+5874_127+5879d others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(1): Show |
G | 87 | a0001c0001t0002g0078 a0001c0001t0002g0084 a0001c0001t0002g0085 others(84): Show |
90 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(87): Show |
intron_variant | MODIFIER | c.127+5872_127+5879d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(3): Show |
G | 17 | a0001c0001t0002g0066 a0001c0001t0004g0356 a0001c0001t0011g0142 others(14): Show |
17 | HG00735.hp2 HG01070.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+5870_127+5879d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(5): Show |
G | 10 | a0001c0001t0002g0092 a0001c0001t0002g0115 a0001c0001t0004g0322 others(7): Show |
10 | HG01358.hp1 NA18942.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+5868_127+5879d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(7): Show |
G | 12 | a0001c0001t0002g0064 a0001c0001t0003g0077 a0001c0001t0003g0079 others(9): Show |
12 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.127+5866_127+5879d others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(9): Show |
G | 11 | a0001c0001t0007g0312 a0003c0003t0005g0037 a0003c0003t0008g0033 others(8): Show |
11 | HG01109.hp2 HG01975.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+5864_127+5879d others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(11): Show |
G | 40 | a0001c0001t0002g0093 a0001c0001t0004g0024 a0001c0016t0002g0051 others(37): Show |
41 | HG00609.hp2 HG00621.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.127+5862_127+5879d others(20): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(13): Show |
G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+5860_127+5879d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(17): Show |
G | 1 | a0003c0003t0018g0225 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.127+5856_127+5879d others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919287 | GTCTCTCT others(33): Show |
G | 4 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(1): Show |
5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+5840_127+5879d others(42): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919287 | ||||||
chr4:109919291 | C | G | 1 | a0002c0002t0001g0157 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.127+5829C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919291 | |||||||
chr4:109919293 | C | G | 1 | a0001c0001t0015g0373 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127+5831C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919293 | |||||||
chr4:109919297 | C | G | 4 | a0001c0001t0011g0146 a0001c0001t0011g0147 a0001c0001t0011g0148 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5835C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919297 | |||||||
chr4:109919299 | C | G | 1 | a0001c0001t0012g0372 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127+5837C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919299 | |||||||
chr4:109919301 | C | G | 1 | a0001c0001t0022g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.127+5839C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919301 | |||||||
chr4:109919303 | C | G | 7 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(4): Show |
7 | HG00735.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+5841C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919303 | |||||||
chr4:109919323 | C | T | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+5861C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919323 | |||||||
chr4:109919428 | T | C | 1 | a0004c0004t0003g0250 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127+5966T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919428 | |||||||
chr4:109919429 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+5967T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919429 | |||||||
chr4:109919450 | C | A | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127+5988C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919450 | |||||||
chr4:109919540 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+6078G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919540 | |||||||
chr4:109919552 | G | A | 1 | a0003c0003t0005g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.127+6090G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919552 | |||||||
chr4:109919582 | AAGAGGAC others(4991): Show |
A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+6123_127+11120 others(3): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109919582 | ||||||
chr4:109919592 | C | T | 269 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(266): Show |
277 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.127+6130C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919592 | |||||||
chr4:109919629 | T | C | 3 | a0001c0001t0012g0372 a0001c0001t0015g0371 a0001c0001t0015g0373 |
3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+6167T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919629 | |||||||
chr4:109919630 | G | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+6168G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919630 | |||||||
chr4:109919635 | G | T | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+6173G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919635 | |||||||
chr4:109919655 | G | A | 1 | a0002c0002t0001g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127+6193G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919655 | |||||||
chr4:109919711 | G | A | 135 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(132): Show |
138 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.127+6249G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919711 | |||||||
chr4:109919790 | A | G | 253 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(250): Show |
261 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.127+6328A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919790 | |||||||
chr4:109919858 | A | G | 1 | a0005c0005t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+6396A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919858 | |||||||
chr4:109919870 | C | A | 71 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(68): Show |
75 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.127+6408C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919870 | |||||||
chr4:109919936 | T | A | 1 | a0002c0002t0001g0169 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.127+6474T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919936 | |||||||
chr4:109919981 | G | A | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+6519G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109919981 | |||||||
chr4:109920274 | T | C | 11 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(8): Show |
11 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+6812T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920274 | |||||||
chr4:109920565 | C | A | 1 | a0001c0007t0002g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.127+7103C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920565 | |||||||
chr4:109920643 | A | G | 4 | a0002c0002t0001g0192 a0002c0002t0001g0193 a0002c0002t0001g0194 others(1): Show |
4 | HG00438.hp1 NA18983.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+7181A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920643 | |||||||
chr4:109920745 | A | T | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+7283A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920745 | |||||||
chr4:109920864 | G | A | 41 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(38): Show |
42 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.127+7402G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109920864 | |||||||
chr4:109921253 | T | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+7791T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921253 | |||||||
chr4:109921253 | T | TAGAAACT others(627): Show |
1 | a0001c0001t0014g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127+7807_127+7808i others(636): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109921253 | ||||||
chr4:109921253 | T | TAGAAACT others(636): Show |
4 | a0001c0001t0012g0232 a0001c0001t0020g0011 a0001c0001t0020g0230 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+7807_127+7808i others(645): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109921253 | ||||||
chr4:109921262 | C | T | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+7800C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921262 | |||||||
chr4:109921357 | T | G | 1 | a0002c0002t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.127+7895T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921357 | |||||||
chr4:109921398 | T | C | 2 | a0004c0004t0003g0254 a0004c0004t0003g0263 |
2 | NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.127+7936T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921398 | |||||||
chr4:109921399 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+7937T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921399 | |||||||
chr4:109921625 | C | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+8163C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921625 | |||||||
chr4:109921652 | C | T | 1 | a0003c0003t0005g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.127+8190C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921652 | |||||||
chr4:109921720 | A | G | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+8258A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921720 | |||||||
chr4:109921728 | A | C | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+8266A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921728 | |||||||
chr4:109921822 | T | C | 1 | a0004c0004t0010g0272 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127+8360T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921822 | |||||||
chr4:109921877 | G | C | 11 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(8): Show |
11 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+8415G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921877 | |||||||
chr4:109921984 | T | C | 134 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(131): Show |
139 | HG00323.hp2 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.127+8522T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921984 | |||||||
chr4:109921992 | T | G | 207 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(204): Show |
214 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.127+8530T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109921992 | |||||||
chr4:109922075 | A | G | 1 | a0002c0002t0021g0314 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.127+8613A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922075 | |||||||
chr4:109922086 | A | C | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127+8624A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922086 | |||||||
chr4:109922104 | A | G | 269 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(266): Show |
277 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.127+8642A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922104 | |||||||
chr4:109922143 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+8681C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922143 | |||||||
chr4:109922182 | G | T | 3 | a0001c0001t0011g0146 a0001c0001t0011g0147 a0001c0001t0011g0148 |
3 | HG02622.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127+8720G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922182 | |||||||
chr4:109922272 | C | G | 50 | a0001c0001t0004g0316 a0001c0001t0004g0320 a0001c0001t0004g0321 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.127+8810C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922272 | |||||||
chr4:109922297 | T | C | 1 | a0003c0003t0018g0168 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.127+8835T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922297 | |||||||
chr4:109922687 | G | A | 1 | a0001c0019t0017g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+9225G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922687 | |||||||
chr4:109922794 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+9332C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922794 | |||||||
chr4:109922835 | T | C | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+9373T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109922835 | |||||||
chr4:109923092 | C | A | 1 | a0002c0002t0001g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127+9630C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923092 | |||||||
chr4:109923174 | T | A | 3 | a0001c0001t0012g0372 a0001c0001t0015g0371 a0001c0001t0015g0373 |
3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127+9712T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923174 | |||||||
chr4:109923326 | A | G | 9 | a0001c0001t0012g0232 a0001c0001t0014g0229 a0001c0001t0014g0235 others(6): Show |
9 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+9864A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923326 | |||||||
chr4:109923659 | C | T | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+10197C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923659 | |||||||
chr4:109923827 | C | A | 1 | a0002c0002t0001g0010 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.127+10365C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923827 | |||||||
chr4:109923848 | T | C | 1 | a0001c0001t0004g0330 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.127+10386T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923848 | |||||||
chr4:109923929 | T | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+10467T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109923929 | |||||||
chr4:109924056 | C | T | 1 | a0002c0002t0006g0366 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.127+10594C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924056 | |||||||
chr4:109924212 | C | T | 1 | a0005c0005t0007g0275 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127+10750C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924212 | |||||||
chr4:109924333 | C | CA | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+10879dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109924333 | ||||||
chr4:109924395 | T | C | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+10933T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924395 | |||||||
chr4:109924467 | C | T | 1 | a0001c0001t0004g0339 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.127+11005C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924467 | |||||||
chr4:109924508 | T | C | 1 | a0001c0001t0004g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127+11046T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924508 | |||||||
chr4:109924523 | G | GACATCAC others(6): Show |
4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+11066_127+1107 others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109924523 | ||||||
chr4:109924551 | T | C | 253 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(250): Show |
261 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.127+11089T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924551 | |||||||
chr4:109924607 | A | G | 276 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(273): Show |
284 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.127+11145A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924607 | |||||||
chr4:109924690 | G | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+11228G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924690 | |||||||
chr4:109924730 | T | G | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.127+11268T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924730 | |||||||
chr4:109924807 | G | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+11345G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109924807 | |||||||
chr4:109924961 | CCATCAGG others(901): Show |
C | 1 | a0001c0001t0004g0353 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.127+11502_127+1240 others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109924961 | ||||||
chr4:109925223 | C | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+11761C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925223 | |||||||
chr4:109925226 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.127+11764C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925226 | |||||||
chr4:109925361 | G | A | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+11899G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925361 | |||||||
chr4:109925481 | A | T | 1 | a0006c0006t0009g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127+12019A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925481 | |||||||
chr4:109925640 | A | G | 120 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(117): Show |
123 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.127+12178A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925640 | |||||||
chr4:109925758 | C | T | 5 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0310 others(2): Show |
5 | NA18963.hp2 NA18967.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+12296C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925758 | |||||||
chr4:109925953 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+12491T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109925953 | |||||||
chr4:109926041 | A | G | 1 | a0002c0002t0001g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127+12579A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926041 | |||||||
chr4:109926245 | C | T | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+12783C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926245 | |||||||
chr4:109926350 | C | CT | 32 | a0001c0001t0002g0066 a0001c0001t0002g0076 a0001c0001t0002g0104 others(29): Show |
32 | HG00423.hp2 HG00733.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+12908dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109926350 | ||||||
chr4:109926350 | CT | C | 116 | a0001c0001t0004g0120 a0001c0001t0004g0291 a0001c0001t0004g0292 others(113): Show |
120 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.127+12908delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109926350 | ||||||
chr4:109926392 | T | A | 1 | a0005c0005t0019g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+12930T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926392 | |||||||
chr4:109926430 | C | T | 3 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0020c0029t0031g0234 |
3 | HG02809.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.127+12968C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926430 | |||||||
chr4:109926509 | C | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+13047C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926509 | |||||||
chr4:109926512 | A | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+13050A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926512 | |||||||
chr4:109926568 | A | G | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+13106A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926568 | |||||||
chr4:109926633 | T | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.127+13171T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926633 | |||||||
chr4:109926690 | G | T | 1 | a0001c0001t0040g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+13228G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926690 | |||||||
chr4:109926693 | A | G | 1 | a0024c0022t0006g0286 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127+13231A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926693 | |||||||
chr4:109926988 | C | T | 1 | a0003c0003t0005g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.127+13526C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109926988 | |||||||
chr4:109927152 | G | A | 48 | a0001c0001t0004g0316 a0001c0001t0004g0320 a0001c0001t0004g0321 others(45): Show |
48 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.127+13690G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927152 | |||||||
chr4:109927163 | T | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(75): Show |
81 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.127+13701T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927163 | |||||||
chr4:109927206 | C | G | 7 | a0001c0007t0002g0006 a0001c0007t0002g0100 a0001c0007t0002g0101 others(4): Show |
8 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-13740C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927206 | |||||||
chr4:109927462 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-13484T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927462 | |||||||
chr4:109927496 | A | G | 258 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(255): Show |
266 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.128-13450A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927496 | |||||||
chr4:109927579 | T | C | 212 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(209): Show |
219 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.128-13367T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927579 | |||||||
chr4:109927587 | G | A | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.128-13359G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927587 | |||||||
chr4:109927596 | C | T | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-13350C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927596 | |||||||
chr4:109927638 | A | G | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-13308A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927638 | |||||||
chr4:109927641 | G | T | 1 | a0002c0002t0001g0216 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128-13305G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927641 | |||||||
chr4:109927642 | C | T | 1 | a0002c0002t0001g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.128-13304C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927642 | |||||||
chr4:109927648 | C | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-13298C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927648 | |||||||
chr4:109927719 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.128-13227G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927719 | |||||||
chr4:109927723 | C | CA | 31 | a0001c0001t0002g0071 a0001c0001t0002g0104 a0001c0001t0004g0291 others(28): Show |
32 | HG00140.hp2 HG01069.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.128-13205dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927723 | ||||||
chr4:109927723 | CA | C | 51 | a0001c0001t0004g0024 a0001c0001t0012g0212 a0001c0001t0012g0214 others(48): Show |
52 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.128-13205delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927723 | ||||||
chr4:109927760 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.128-13186T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927760 | |||||||
chr4:109927806 | C | CGT | 39 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0007g0312 others(36): Show |
40 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-13098_128-1309 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | C | CGTGT | 19 | a0002c0002t0009g0215 a0003c0003t0005g0054 a0004c0004t0003g0277 others(16): Show |
20 | HG01975.hp2 HG01978.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.128-13100_128-1309 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | C | CGTGTGT | 4 | a0003c0003t0008g0059 a0004c0004t0003g0281 a0005c0005t0007g0282 others(1): Show |
4 | HG02965.hp1 NA18947.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-13102_128-1309 others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGT | C | 161 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(158): Show |
166 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.128-13098_128-1309 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGTGT | C | 63 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(60): Show |
66 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.128-13100_128-1309 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGTGTGT | C | 8 | a0001c0001t0004g0024 a0001c0001t0012g0372 a0001c0001t0015g0371 others(5): Show |
8 | HG00738.hp1 HG01515.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-13102_128-1309 others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGTGTGTG others(3): Show |
C | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-13106_128-1309 others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGTGTGTG others(5): Show |
C | 1 | a0002c0002t0001g0167 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.128-13108_128-1309 others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGTGTGTG others(7): Show |
C | 2 | a0002c0002t0001g0165 a0002c0002t0001g0166 |
2 | HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.128-13110_128-1309 others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927806 | CGTGTGTG others(9): Show |
C | 1 | a0006c0006t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.128-13112_128-1309 others(20): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927806 | ||||||
chr4:109927846 | T | A | 1 | a0001c0013t0002g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.128-13100T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927846 | |||||||
chr4:109927848 | T | A | 125 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(122): Show |
129 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.128-13098T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109927848 | |||||||
chr4:109927848 | T | TGA | 9 | a0001c0001t0004g0362 a0001c0001t0022g0236 a0001c0001t0022g0239 others(6): Show |
9 | HG00735.hp2 HG01167.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-13097_128-1309 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927848 | ||||||
chr4:109927848 | T | TGTGTGTG others(1): Show |
3 | a0012c0014t0007g0138 a0013c0017t0007g0136 a0013c0017t0007g0137 |
3 | HG02257.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.128-13097_128-1309 others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927848 | ||||||
chr4:109927848 | T | TGTGTGTG others(5): Show |
1 | a0012c0014t0007g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128-13097_128-1309 others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109927848 | ||||||
chr4:109928352 | G | C | 64 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(61): Show |
67 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.128-12594G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928352 | |||||||
chr4:109928399 | C | A | 2 | a0001c0001t0011g0142 a0001c0001t0011g0145 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.128-12547C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928399 | |||||||
chr4:109928613 | C | T | 11 | a0005c0005t0007g0001 a0005c0005t0007g0241 a0005c0005t0007g0275 others(8): Show |
12 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-12333C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928613 | |||||||
chr4:109928706 | C | T | 6 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(3): Show |
7 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-12240C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928706 | |||||||
chr4:109928971 | T | C | 1 | a0001c0026t0002g0096 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.128-11975T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109928971 | |||||||
chr4:109929226 | T | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-11720T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929226 | |||||||
chr4:109929307 | C | G | 3 | a0001c0001t0012g0372 a0001c0001t0015g0371 a0001c0001t0015g0373 |
3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.128-11639C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929307 | |||||||
chr4:109929320 | G | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-11626G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929320 | |||||||
chr4:109929714 | A | AT | 65 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(62): Show |
68 | HG00558.hp1 HG00597.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.128-11225dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109929714 | ||||||
chr4:109929912 | T | C | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-11034T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929912 | |||||||
chr4:109929980 | G | A | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-10966G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109929980 | |||||||
chr4:109930017 | T | G | 3 | a0001c0001t0012g0372 a0001c0001t0015g0371 a0001c0001t0015g0373 |
3 | HG01891.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.128-10929T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930017 | |||||||
chr4:109930220 | A | G | 2 | a0002c0002t0001g0202 a0002c0002t0001g0203 |
2 | HG04184.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.128-10726A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930220 | |||||||
chr4:109930234 | A | G | 1 | a0005c0005t0007g0275 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128-10712A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930234 | |||||||
chr4:109930815 | G | A | 5 | a0002c0002t0021g0314 a0007c0008t0003g0317 a0007c0008t0003g0318 others(2): Show |
5 | NA18939.hp2 NA18947.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-10131G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930815 | |||||||
chr4:109930854 | A | G | 1 | a0003c0003t0005g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.128-10092A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930854 | |||||||
chr4:109930899 | C | G | 1 | a0001c0001t0002g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.128-10047C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930899 | |||||||
chr4:109930910 | C | A | 1 | a0004c0004t0003g0302 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.128-10036C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930910 | |||||||
chr4:109930981 | AT | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-9964delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109930981 | |||||||
chr4:109931154 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.128-9792C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109931154 | |||||||
chr4:109931303 | A | G | 144 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(141): Show |
148 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.128-9643A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109931303 | |||||||
chr4:109931769 | C | T | 1 | a0010c0011t0001g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.128-9177C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109931769 | |||||||
chr4:109932057 | G | A | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-8889G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932057 | |||||||
chr4:109932075 | T | A | 65 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(62): Show |
68 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.128-8871T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932075 | |||||||
chr4:109932081 | A | C | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8865A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932081 | |||||||
chr4:109932186 | C | T | 73 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(70): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-8760C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932186 | |||||||
chr4:109932187 | G | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-8759G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932187 | |||||||
chr4:109932324 | C | CT | 121 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(118): Show |
124 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.128-8609dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932324 | ||||||
chr4:109932360 | C | CATATATA others(1): Show |
3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02895.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.128-8576_128-8569d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(15): Show |
1 | a0001c0001t0015g0373 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(24): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(17): Show |
5 | a0001c0001t0002g0115 a0001c0001t0003g0079 a0001c0001t0018g0233 others(2): Show |
5 | HG00673.hp1 HG02129.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(19): Show |
17 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(14): Show |
17 | HG00673.hp2 HG01928.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(21): Show |
47 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0076 others(44): Show |
50 | HG00323.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(30): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(23): Show |
26 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0075 others(23): Show |
26 | HG01167.hp1 HG01167.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(32): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(25): Show |
1 | a0001c0001t0002g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(34): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(27): Show |
1 | a0001c0007t0002g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(36): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(61): Show |
1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(70): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932360 | C | CATATATA others(33): Show |
1 | a0001c0001t0002g0307 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(42): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932360 | ||||||
chr4:109932363 | A | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-8583A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932363 | |||||||
chr4:109932376 | T | TATATA | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(18): Show |
1 | a0001c0001t0011g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(19): Show |
2 | a0001c0001t0004g0316 a0001c0001t0013g0337 |
2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(21): Show |
9 | a0001c0001t0004g0320 a0001c0001t0004g0321 a0001c0001t0004g0322 others(6): Show |
9 | HG00408.hp1 HG00438.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(30): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(22): Show |
1 | a0001c0001t0003g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(31): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(23): Show |
7 | a0001c0001t0004g0328 a0001c0001t0004g0329 a0001c0001t0013g0348 others(4): Show |
7 | NA18939.hp2 NA18947.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-8569_128-8568i others(32): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(24): Show |
1 | a0007c0008t0003g0319 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(33): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932376 | T | TATATATA others(25): Show |
3 | a0001c0001t0004g0334 a0001c0001t0013g0340 a0007c0008t0003g0369 |
3 | NA18985.hp2 NA18998.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(34): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932376 | ||||||
chr4:109932377 | A | ATATATAT others(16): Show |
2 | a0001c0001t0004g0338 a0001c0019t0017g0141 |
2 | HG02615.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(25): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | |||||||
chr4:109932377 | A | ATATATAT others(18): Show |
2 | a0001c0001t0004g0293 a0016c0030t0016g0305 |
2 | HG00738.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | |||||||
chr4:109932377 | A | ATATATAT others(20): Show |
2 | a0001c0001t0002g0113 a0001c0001t0006g0114 |
2 | NA18945.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.128-8569_128-8568i others(29): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | |||||||
chr4:109932377 | A | ATATATAT others(22): Show |
1 | a0001c0019t0007g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.128-8569_128-8568i others(31): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | |||||||
chr4:109932377 | A | ATATATAT others(24): Show |
1 | a0001c0001t0004g0360 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(33): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | |||||||
chr4:109932377 | A | ATATATAT others(26): Show |
1 | a0001c0001t0004g0361 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.128-8569_128-8568i others(35): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932377 | |||||||
chr4:109932378 | A | T | 47 | a0001c0001t0002g0104 a0001c0001t0004g0024 a0001c0016t0002g0051 others(44): Show |
48 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.128-8568A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932378 | |||||||
chr4:109932379 | A | T | 10 | a0001c0001t0003g0088 a0001c0001t0011g0146 a0007c0008t0003g0319 others(7): Show |
10 | HG00621.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-8567A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932379 | |||||||
chr4:109932379 | AT | A | 25 | a0005c0005t0006g0245 a0005c0005t0006g0248 a0005c0005t0007g0001 others(22): Show |
27 | HG01109.hp2 HG01255.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.128-8550delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109932379 | ||||||
chr4:109932380 | T | A | 8 | a0001c0001t0002g0113 a0001c0001t0004g0293 a0001c0001t0004g0338 others(5): Show |
8 | HG00738.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-8566T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932380 | |||||||
chr4:109932380 | T | TATATATA others(18): Show |
1 | a0003c0003t0005g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-8566_128-8565i others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932380 | |||||||
chr4:109932380 | T | TATATATA others(19): Show |
1 | a0001c0001t0002g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.128-8566_128-8565i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932380 | |||||||
chr4:109932381 | T | A | 45 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.128-8565T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932381 | |||||||
chr4:109932382 | T | A | 1 | a0003c0003t0005g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-8564T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(13): Show |
1 | a0003c0003t0005g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.128-8564_128-8563i others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(15): Show |
5 | a0003c0003t0005g0022 a0003c0003t0005g0028 a0003c0003t0008g0056 others(2): Show |
5 | HG02027.hp1 HG03239.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(24): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(17): Show |
8 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(5): Show |
8 | HG00621.hp1 HG03017.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(19): Show |
17 | a0003c0003t0005g0002 a0003c0003t0005g0019 a0003c0003t0005g0026 others(14): Show |
17 | HG00423.hp1 HG02015.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(21): Show |
7 | a0003c0003t0005g0003 a0003c0003t0005g0023 a0003c0003t0005g0043 others(4): Show |
8 | NA18945.hp1 NA18953.hp1 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(30): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(23): Show |
4 | a0003c0003t0005g0025 a0003c0003t0005g0048 a0003c0003t0008g0046 others(1): Show |
4 | HG00609.hp2 HG02080.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-8564_128-8563i others(32): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(25): Show |
1 | a0003c0003t0005g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.128-8564_128-8563i others(34): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932382 | T | TATATATA others(27): Show |
1 | a0003c0003t0005g0049 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.128-8564_128-8563i others(36): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932382 | |||||||
chr4:109932383 | T | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-8563T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932383 | |||||||
chr4:109932405 | G | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-8541G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932405 | |||||||
chr4:109932415 | G | C | 1 | a0001c0001t0022g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.128-8531G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932415 | |||||||
chr4:109932519 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.128-8427C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932519 | |||||||
chr4:109932539 | T | G | 1 | a0002c0002t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.128-8407T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932539 | |||||||
chr4:109932546 | T | G | 2 | a0006c0006t0001g0294 a0006c0006t0001g0295 |
2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.128-8400T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932546 | |||||||
chr4:109932554 | A | G | 1 | a0003c0003t0005g0048 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.128-8392A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932554 | |||||||
chr4:109932599 | C | T | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-8347C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932599 | |||||||
chr4:109932600 | G | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-8346G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932600 | |||||||
chr4:109932621 | G | A | 136 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(133): Show |
139 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.128-8325G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932621 | |||||||
chr4:109932659 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.128-8287G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932659 | |||||||
chr4:109932679 | G | A | 1 | a0005c0005t0017g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.128-8267G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932679 | |||||||
chr4:109932857 | C | A | 1 | a0001c0001t0004g0361 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.128-8089C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109932857 | |||||||
chr4:109933160 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-7786C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933160 | |||||||
chr4:109933187 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.128-7759C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933187 | |||||||
chr4:109933275 | G | A | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-7671G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933275 | |||||||
chr4:109933379 | A | G | 1 | a0004c0004t0003g0277 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.128-7567A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933379 | |||||||
chr4:109933388 | C | T | 143 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(140): Show |
146 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.128-7558C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933388 | |||||||
chr4:109933424 | CT | C | 125 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(122): Show |
129 | HG00323.hp2 HG00423.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.128-7508delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109933424 | ||||||
chr4:109933439 | A | G | 7 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-7507A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933439 | |||||||
chr4:109933532 | C | T | 3 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0022c0035t0017g0126 |
3 | HG02615.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.128-7414C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933532 | |||||||
chr4:109933533 | G | C | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.128-7413G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933533 | |||||||
chr4:109933557 | C | T | 1 | a0002c0002t0036g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.128-7389C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933557 | |||||||
chr4:109933596 | C | T | 2 | a0010c0011t0001g0199 a0010c0011t0001g0219 |
2 | NA18956.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.128-7350C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933596 | |||||||
chr4:109933668 | C | T | 59 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.128-7278C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933668 | |||||||
chr4:109933761 | T | A | 1 | a0004c0004t0004g0260 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.128-7185T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933761 | |||||||
chr4:109933781 | C | T | 6 | a0005c0005t0011g0342 a0009c0010t0016g0344 a0009c0010t0016g0345 others(3): Show |
6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-7165C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933781 | |||||||
chr4:109933783 | T | C | 1 | a0002c0002t0001g0169 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.128-7163T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933783 | |||||||
chr4:109933784 | G | C | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128-7162G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933784 | |||||||
chr4:109933893 | A | G | 192 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(189): Show |
196 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.128-7053A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109933893 | |||||||
chr4:109934023 | A | G | 1 | a0001c0001t0014g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.128-6923A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934023 | |||||||
chr4:109934237 | T | C | 1 | a0002c0002t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128-6709T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934237 | |||||||
chr4:109934255 | G | A | 1 | a0002c0002t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.128-6691G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934255 | |||||||
chr4:109934270 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-6676G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934270 | |||||||
chr4:109934399 | T | G | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-6547T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934399 | |||||||
chr4:109934427 | ATTTG | A | 4 | a0001c0001t0002g0078 a0001c0001t0003g0077 a0001c0001t0003g0079 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-6515_128-6512d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109934427 | ||||||
chr4:109934443 | T | C | 1 | a0001c0001t0011g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.128-6503T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934443 | |||||||
chr4:109934629 | C | T | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-6317C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934629 | |||||||
chr4:109934685 | A | G | 1 | a0003c0003t0005g0048 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.128-6261A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934685 | |||||||
chr4:109934719 | A | G | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-6227A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934719 | |||||||
chr4:109934781 | T | G | 192 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(189): Show |
196 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.128-6165T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934781 | |||||||
chr4:109934795 | C | T | 67 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(64): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-6151C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934795 | |||||||
chr4:109934802 | C | T | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.128-6144C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934802 | |||||||
chr4:109934837 | G | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-6109G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934837 | |||||||
chr4:109934943 | C | T | 11 | a0005c0005t0007g0001 a0005c0005t0007g0241 a0005c0005t0007g0275 others(8): Show |
12 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-6003C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109934943 | |||||||
chr4:109935036 | G | T | 59 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.128-5910G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935036 | |||||||
chr4:109935041 | A | G | 67 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(64): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-5905A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935041 | |||||||
chr4:109935169 | G | T | 1 | a0003c0003t0008g0045 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.128-5777G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935169 | |||||||
chr4:109935186 | T | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-5760T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935186 | |||||||
chr4:109935278 | TC | T | 3 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0022c0035t0017g0126 |
3 | HG02615.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.128-5665delC | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109935278 | ||||||
chr4:109935323 | A | G | 2 | a0006c0006t0001g0294 a0006c0006t0001g0295 |
2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.128-5623A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935323 | |||||||
chr4:109935368 | A | G | 7 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-5578A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935368 | |||||||
chr4:109935406 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.128-5540A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935406 | |||||||
chr4:109935447 | T | C | 67 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(64): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-5499T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935447 | |||||||
chr4:109935456 | G | A | 49 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5490G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935456 | |||||||
chr4:109935475 | G | A | 49 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5471G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935475 | |||||||
chr4:109935476 | G | A | 49 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5470G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935476 | |||||||
chr4:109935483 | A | G | 49 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-5463A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935483 | |||||||
chr4:109935530 | T | C | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-5416T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935530 | |||||||
chr4:109935628 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-5318T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935628 | |||||||
chr4:109935759 | T | A | 1 | a0002c0002t0001g0160 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.128-5187T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935759 | |||||||
chr4:109935870 | C | G | 31 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(28): Show |
32 | HG00558.hp1 HG00597.hp2 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.128-5076C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935870 | |||||||
chr4:109935900 | C | T | 55 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(52): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.128-5046C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935900 | |||||||
chr4:109935957 | T | C | 1 | a0005c0005t0017g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.128-4989T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935957 | |||||||
chr4:109935970 | T | C | 1 | a0002c0002t0001g0303 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.128-4976T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109935970 | |||||||
chr4:109936011 | T | C | 53 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(50): Show |
55 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.128-4935T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936011 | |||||||
chr4:109936093 | A | G | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-4853A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936093 | |||||||
chr4:109936137 | G | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-4809G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936137 | |||||||
chr4:109936311 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-4635C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936311 | |||||||
chr4:109936319 | G | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-4627G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936319 | |||||||
chr4:109936372 | T | A | 6 | a0001c0001t0002g0004 a0001c0001t0002g0084 a0001c0001t0002g0085 others(3): Show |
7 | HG01167.hp2 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-4574T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936372 | |||||||
chr4:109936383 | G | A | 1 | a0002c0002t0006g0335 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.128-4563G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936383 | |||||||
chr4:109936613 | G | A | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128-4333G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936613 | |||||||
chr4:109936627 | T | G | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.128-4319T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936627 | |||||||
chr4:109936667 | T | A | 1 | a0003c0003t0005g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.128-4279T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936667 | |||||||
chr4:109936686 | C | A | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-4260C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936686 | |||||||
chr4:109936790 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-4156G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936790 | |||||||
chr4:109936897 | C | T | 1 | a0001c0001t0015g0373 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.128-4049C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936897 | |||||||
chr4:109936959 | C | T | 2 | a0001c0001t0004g0361 a0003c0003t0008g0056 |
2 | HG00733.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.128-3987C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109936959 | |||||||
chr4:109937108 | G | A | 1 | a0002c0002t0001g0152 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.128-3838G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937108 | |||||||
chr4:109937137 | T | C | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-3809T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937137 | |||||||
chr4:109937144 | C | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3802C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937144 | |||||||
chr4:109937318 | C | G | 268 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(265): Show |
275 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.128-3628C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937318 | |||||||
chr4:109937359 | CT | C | 124 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0006g0249 others(121): Show |
129 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.128-3572delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109937359 | ||||||
chr4:109937359 | CTT | C | 145 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(142): Show |
148 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.128-3573_128-3572d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109937359 | ||||||
chr4:109937537 | A | G | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-3409A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937537 | |||||||
chr4:109937652 | G | A | 7 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-3294G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937652 | |||||||
chr4:109937824 | A | G | 67 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(64): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-3122A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937824 | |||||||
chr4:109937893 | A | G | 67 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(64): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-3053A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937893 | |||||||
chr4:109937935 | G | T | 1 | a0023c0024t0007g0280 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.128-3011G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109937935 | |||||||
chr4:109938006 | C | T | 1 | a0001c0001t0004g0327 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.128-2940C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938006 | |||||||
chr4:109938020 | G | A | 4 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(1): Show |
5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2926G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938020 | |||||||
chr4:109938024 | G | A | 3 | a0003c0003t0005g0019 a0003c0003t0005g0055 a0003c0003t0018g0225 |
3 | HG02040.hp2 HG02074.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.128-2922G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938024 | |||||||
chr4:109938222 | T | C | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-2724T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938222 | |||||||
chr4:109938281 | A | G | 1 | a0004c0032t0003g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.128-2665A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938281 | |||||||
chr4:109938323 | C | T | 1 | a0004c0004t0010g0261 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.128-2623C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938323 | |||||||
chr4:109938419 | C | T | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-2527C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938419 | |||||||
chr4:109938538 | T | C | 1 | a0001c0001t0014g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.128-2408T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938538 | |||||||
chr4:109938619 | C | CT | 6 | a0005c0005t0011g0342 a0009c0010t0016g0344 a0009c0010t0016g0345 others(3): Show |
6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2322dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 109938619 | ||||||
chr4:109938712 | T | C | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-2234T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938712 | |||||||
chr4:109938824 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG00735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.128-2122T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109938824 | |||||||
chr4:109939022 | G | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-1924G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939022 | |||||||
chr4:109939067 | G | T | 1 | a0001c0001t0006g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.128-1879G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939067 | |||||||
chr4:109939165 | G | A | 5 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(2): Show |
6 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-1781G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939165 | |||||||
chr4:109939233 | A | G | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.128-1713A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939233 | |||||||
chr4:109939295 | A | T | 3 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 |
3 | HG00621.hp2 HG00673.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.128-1651A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939295 | |||||||
chr4:109939303 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-1643G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939303 | |||||||
chr4:109939308 | C | A | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1638C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939308 | |||||||
chr4:109939369 | G | T | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1577G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939369 | |||||||
chr4:109939389 | G | A | 6 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(3): Show |
7 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-1557G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939389 | |||||||
chr4:109939399 | C | T | 5 | a0006c0006t0001g0163 a0011c0012t0014g0226 a0011c0012t0014g0227 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-1547C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939399 | |||||||
chr4:109939458 | G | C | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-1488G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939458 | |||||||
chr4:109939513 | C | T | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1433C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939513 | |||||||
chr4:109939523 | C | T | 54 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.128-1423C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939523 | |||||||
chr4:109939640 | T | C | 1 | a0002c0002t0001g0133 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.128-1306T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939640 | |||||||
chr4:109939661 | C | T | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-1285C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939661 | |||||||
chr4:109939662 | G | A | 5 | a0002c0002t0001g0169 a0002c0002t0001g0171 a0002c0002t0009g0150 others(2): Show |
5 | HG02293.hp2 HG02300.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-1284G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939662 | |||||||
chr4:109939681 | A | G | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-1265A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939681 | |||||||
chr4:109939705 | G | A | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-1241G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939705 | |||||||
chr4:109939717 | G | T | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1229G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109939717 | |||||||
chr4:109940071 | G | A | 1 | a0001c0001t0040g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.128-875G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940071 | |||||||
chr4:109940236 | G | A | 1 | a0001c0001t0006g0107 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-710G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940236 | |||||||
chr4:109940271 | G | A | 1 | a0002c0002t0012g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.128-675G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940271 | |||||||
chr4:109940284 | T | C | 2 | a0005c0005t0007g0278 a0005c0005t0007g0282 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.128-662T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940284 | |||||||
chr4:109940313 | T | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.128-633T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940313 | |||||||
chr4:109940357 | T | C | 2 | a0001c0001t0011g0142 a0001c0001t0011g0145 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.128-589T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940357 | |||||||
chr4:109940487 | G | A | 59 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.128-459G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940487 | |||||||
chr4:109940628 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.128-318A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940628 | |||||||
chr4:109940760 | C | T | 2 | a0001c0001t0004g0347 a0004c0032t0003g0262 |
2 | NA18975.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.128-186C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940760 | |||||||
chr4:109940771 | G | A | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-175G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940771 | |||||||
chr4:109940785 | T | G | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128-161T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940785 | |||||||
chr4:109940867 | G | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-79G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940867 | |||||||
chr4:109940882 | G | A | 2 | a0004c0004t0003g0254 a0004c0004t0003g0263 |
2 | NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.128-64G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 1/23 | chr4 | 109940882 | |||||||
chr4:109941207 | C | T | 50 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(47): Show |
51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.327+62C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941207 | |||||||
chr4:109941257 | G | A | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.327+112G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941257 | |||||||
chr4:109941271 | T | C | 2 | a0001c0016t0002g0051 a0001c0016t0006g0029 |
2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.327+126T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941271 | |||||||
chr4:109941289 | A | G | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.327+144A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941289 | |||||||
chr4:109941480 | T | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.327+335T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941480 | |||||||
chr4:109941481 | G | A | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+336G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941481 | |||||||
chr4:109941489 | A | G | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+344A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941489 | |||||||
chr4:109941526 | C | T | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.327+381C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941526 | |||||||
chr4:109941561 | G | A | 9 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0115 others(6): Show |
9 | NA18942.hp1 NA18946.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.327+416G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941561 | |||||||
chr4:109941575 | G | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327+430G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941575 | |||||||
chr4:109941952 | T | G | 1 | a0003c0003t0005g0030 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.327+807T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109941952 | |||||||
chr4:109942065 | C | A | 4 | a0002c0002t0001g0008 a0002c0002t0001g0151 a0002c0002t0001g0155 others(1): Show |
5 | NA18941.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+920C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942065 | |||||||
chr4:109942202 | T | C | 2 | a0003c0003t0005g0002 a0003c0003t0008g0002 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.328-1052T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942202 | |||||||
chr4:109942257 | T | C | 6 | a0005c0005t0011g0342 a0009c0010t0016g0344 a0009c0010t0016g0345 others(3): Show |
6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-997T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942257 | |||||||
chr4:109942513 | G | A | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-741G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942513 | |||||||
chr4:109942589 | C | T | 4 | a0003c0003t0005g0022 a0003c0003t0005g0023 a0003c0003t0026g0020 others(1): Show |
4 | NA18994.hp2 NA19002.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-665C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942589 | |||||||
chr4:109942663 | A | G | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-591A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942663 | |||||||
chr4:109942779 | G | A | 1 | a0003c0003t0008g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.328-475G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942779 | |||||||
chr4:109942842 | A | G | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.328-412A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942842 | |||||||
chr4:109942852 | G | T | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-402G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942852 | |||||||
chr4:109942897 | T | C | 67 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(64): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.328-357T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109942897 | |||||||
chr4:109943053 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.328-201T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 2/23 | chr4 | 109943053 | |||||||
chr4:109943567 | G | A | 9 | a0005c0005t0007g0001 a0005c0005t0007g0241 a0005c0005t0007g0278 others(6): Show |
10 | HG02572.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+132G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943567 | |||||||
chr4:109943600 | G | A | 2 | a0001c0016t0002g0051 a0001c0016t0006g0029 |
2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.509+165G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943600 | |||||||
chr4:109943674 | T | TA | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-168_510-167ins others(1): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943674 | |||||||
chr4:109943675 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-167G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943675 | |||||||
chr4:109943702 | G | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-140G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943702 | |||||||
chr4:109943773 | A | T | 1 | a0001c0001t0002g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.510-69A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 3/23 | chr4 | 109943773 | |||||||
chr4:109944115 | T | G | 136 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(133): Show |
139 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.737+46T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944115 | |||||||
chr4:109944160 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.737+91G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944160 | |||||||
chr4:109944168 | G | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+99G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944168 | |||||||
chr4:109944169 | G | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+100G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944169 | |||||||
chr4:109944210 | G | A | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+141G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944210 | |||||||
chr4:109944222 | G | T | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+153G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944222 | |||||||
chr4:109944255 | C | T | 1 | a0005c0005t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+186C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944255 | |||||||
chr4:109944270 | T | A | 1 | a0001c0001t0002g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.737+201T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944270 | |||||||
chr4:109944276 | A | G | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.737+207A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944276 | |||||||
chr4:109944309 | A | G | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.737+240A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944309 | |||||||
chr4:109944312 | A | G | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+243A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944312 | |||||||
chr4:109944329 | T | C | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+260T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944329 | |||||||
chr4:109944331 | C | T | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+262C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944331 | |||||||
chr4:109944366 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.737+297G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944366 | |||||||
chr4:109944390 | T | G | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+321T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944390 | |||||||
chr4:109944414 | G | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.737+345G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944414 | |||||||
chr4:109944418 | G | A | 3 | a0004c0004t0003g0264 a0004c0004t0010g0255 a0005c0005t0004g0301 |
3 | HG02129.hp2 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.737+349G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944418 | |||||||
chr4:109944429 | A | C | 1 | a0003c0003t0005g0022 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.737+360A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944429 | |||||||
chr4:109944442 | A | G | 1 | a0002c0002t0001g0209 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.737+373A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944442 | |||||||
chr4:109944552 | A | G | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.737+483A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109944552 | |||||||
chr4:109945022 | A | C | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.738-51A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 4/23 | chr4 | 109945022 | |||||||
chr4:109945286 | G | A | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.940+11G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945286 | |||||||
chr4:109945297 | G | A | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+22G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945297 | |||||||
chr4:109945352 | C | T | 143 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(140): Show |
146 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.940+77C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945352 | |||||||
chr4:109945370 | A | T | 72 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(69): Show |
75 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(72): Show |
intron_variant | MODIFIER | c.940+95A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945370 | |||||||
chr4:109945426 | A | T | 53 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(50): Show |
55 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.940+151A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945426 | |||||||
chr4:109945561 | G | A | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.940+286G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945561 | |||||||
chr4:109945564 | C | T | 3 | a0003c0003t0005g0041 a0003c0003t0005g0044 a0003c0003t0008g0052 |
3 | HG02056.hp1 NA18951.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.940+289C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945564 | |||||||
chr4:109945565 | G | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+290G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109945565 | |||||||
chr4:109945579 | C | CGAAA | 5 | a0005c0005t0019g0012 a0005c0005t0019g0243 a0005c0005t0019g0246 others(2): Show |
6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+321_940+324dup others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109945579 | ||||||
chr4:109945995 | ATTGT | A | 4 | a0002c0002t0001g0008 a0002c0002t0001g0151 a0002c0002t0001g0155 others(1): Show |
5 | NA18941.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+724_940+727del others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109945995 | ||||||
chr4:109946072 | C | A | 59 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.940+797C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946072 | |||||||
chr4:109946194 | G | T | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.940+919G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946194 | |||||||
chr4:109946274 | A | G | 2 | a0005c0005t0006g0245 a0005c0005t0006g0248 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.940+999A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946274 | |||||||
chr4:109946442 | A | G | 1 | a0004c0004t0003g0289 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.940+1167A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946442 | |||||||
chr4:109946523 | A | C | 1 | a0002c0002t0009g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.940+1248A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946523 | |||||||
chr4:109946780 | A | G | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.940+1505A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946780 | |||||||
chr4:109946892 | A | C | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+1617A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946892 | |||||||
chr4:109946930 | C | A | 1 | a0001c0001t0015g0373 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.940+1655C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946930 | |||||||
chr4:109946931 | C | T | 1 | a0002c0002t0006g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.940+1656C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946931 | |||||||
chr4:109946968 | A | C | 5 | a0005c0005t0019g0012 a0005c0005t0019g0243 a0005c0005t0019g0246 others(2): Show |
6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+1693A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946968 | |||||||
chr4:109946987 | C | T | 6 | a0002c0002t0001g0165 a0002c0002t0001g0166 a0002c0002t0001g0206 others(3): Show |
6 | HG01074.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+1712C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109946987 | |||||||
chr4:109947129 | T | TA | 59 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.940+1865dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109947129 | ||||||
chr4:109947163 | C | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+1888C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947163 | |||||||
chr4:109947179 | G | GA | 273 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(270): Show |
281 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.940+1911dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109947179 | ||||||
chr4:109947195 | G | A | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940+1920G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947195 | |||||||
chr4:109947362 | T | C | 6 | a0005c0005t0011g0342 a0009c0010t0016g0344 a0009c0010t0016g0345 others(3): Show |
6 | HG01109.hp2 HG01975.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+2087T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947362 | |||||||
chr4:109947378 | C | A | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+2103C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947378 | |||||||
chr4:109947431 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.940+2156G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947431 | |||||||
chr4:109947552 | C | G | 3 | a0002c0002t0001g0167 a0002c0002t0009g0164 a0002c0002t0009g0205 |
3 | NA18967.hp1 NA18991.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.940+2277C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947552 | |||||||
chr4:109947628 | T | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.940+2353T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947628 | |||||||
chr4:109947712 | T | C | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+2437T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947712 | |||||||
chr4:109947787 | T | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0018 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.940+2512T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947787 | |||||||
chr4:109947911 | T | G | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+2636T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947911 | |||||||
chr4:109947986 | G | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+2711G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109947986 | |||||||
chr4:109948028 | C | A | 5 | a0005c0005t0019g0012 a0005c0005t0019g0243 a0005c0005t0019g0246 others(2): Show |
6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+2753C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948028 | |||||||
chr4:109948043 | C | T | 1 | a0004c0004t0003g0259 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.940+2768C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948043 | |||||||
chr4:109948068 | G | A | 1 | a0005c0005t0013g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.940+2793G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948068 | |||||||
chr4:109948090 | G | A | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.940+2815G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948090 | |||||||
chr4:109948105 | A | G | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.940+2830A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948105 | |||||||
chr4:109948106 | T | A | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.940+2831T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948106 | |||||||
chr4:109948195 | G | A | 1 | a0001c0001t0002g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.940+2920G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948195 | |||||||
chr4:109948497 | G | C | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.940+3222G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948497 | |||||||
chr4:109948497 | G | T | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.940+3222G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948497 | |||||||
chr4:109948529 | G | T | 1 | a0011c0012t0014g0228 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.940+3254G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948529 | |||||||
chr4:109948547 | G | A | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.940+3272G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948547 | |||||||
chr4:109948593 | C | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.940+3318C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948593 | |||||||
chr4:109948660 | G | A | 193 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.940+3385G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948660 | |||||||
chr4:109948678 | G | A | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.940+3403G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948678 | |||||||
chr4:109948990 | A | G | 4 | a0004c0004t0003g0283 a0004c0004t0003g0284 a0004c0004t0003g0285 others(1): Show |
4 | HG01175.hp1 HG02148.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3715A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948990 | |||||||
chr4:109948991 | T | C | 2 | a0004c0004t0003g0253 a0004c0004t0003g0277 |
2 | HG01928.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.940+3716T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109948991 | |||||||
chr4:109949007 | A | C | 3 | a0002c0002t0001g0010 a0002c0002t0001g0197 a0002c0002t0001g0198 |
4 | HG00597.hp1 HG02040.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3732A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949007 | |||||||
chr4:109949070 | T | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.940+3795T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949070 | |||||||
chr4:109949092 | A | G | 1 | a0002c0002t0012g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.940+3817A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949092 | |||||||
chr4:109949097 | C | T | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+3822C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949097 | |||||||
chr4:109949128 | G | A | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.940+3853G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949128 | |||||||
chr4:109949153 | G | A | 1 | a0004c0004t0003g0013 | 2 | NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.940+3878G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949153 | |||||||
chr4:109949238 | T | G | 4 | a0001c0001t0012g0232 a0001c0001t0020g0011 a0001c0001t0020g0230 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3963T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949238 | |||||||
chr4:109949255 | C | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+3980C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949255 | |||||||
chr4:109949297 | C | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+4022C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949297 | |||||||
chr4:109949354 | G | A | 1 | a0001c0001t0004g0330 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.940+4079G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949354 | |||||||
chr4:109949609 | T | C | 81 | a0001c0001t0004g0120 a0001c0001t0006g0249 a0001c0001t0007g0007 others(78): Show |
85 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(82): Show |
intron_variant | MODIFIER | c.940+4334T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949609 | |||||||
chr4:109949618 | CT | C | 21 | a0001c0001t0004g0320 a0001c0001t0004g0360 a0001c0001t0007g0312 others(18): Show |
21 | HG00597.hp1 HG01070.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.940+4357delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109949618 | ||||||
chr4:109949648 | T | A | 1 | a0001c0001t0002g0308 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.940+4373T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949648 | |||||||
chr4:109949937 | G | A | 1 | a0002c0002t0006g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.940+4662G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109949937 | |||||||
chr4:109950013 | C | G | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.940+4738C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950013 | |||||||
chr4:109950077 | C | G | 1 | a0009c0010t0016g0352 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.940+4802C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950077 | |||||||
chr4:109950164 | G | A | 3 | a0005c0005t0019g0012 a0005c0005t0019g0246 a0018c0023t0045g0247 |
4 | HG02559.hp1 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+4889G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950164 | |||||||
chr4:109950293 | G | A | 2 | a0001c0001t0004g0316 a0001c0001t0013g0337 |
2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.940+5018G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950293 | |||||||
chr4:109950297 | C | A | 1 | a0001c0026t0002g0096 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.940+5022C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950297 | |||||||
chr4:109950355 | T | C | 196 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(193): Show |
200 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.940+5080T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950355 | |||||||
chr4:109950380 | A | G | 8 | a0003c0003t0005g0027 a0003c0003t0005g0030 a0003c0003t0005g0039 others(5): Show |
8 | HG00609.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.940+5105A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950380 | |||||||
chr4:109950387 | T | C | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+5112T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950387 | |||||||
chr4:109950411 | C | T | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940+5136C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950411 | |||||||
chr4:109950512 | A | AT | 6 | a0001c0001t0015g0191 a0001c0001t0030g0196 a0002c0002t0001g0192 others(3): Show |
6 | HG00438.hp1 NA18612.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+5238dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109950512 | ||||||
chr4:109950535 | A | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+5260A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950535 | |||||||
chr4:109950670 | C | T | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+5395C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950670 | |||||||
chr4:109950786 | A | G | 1 | a0025c0028t0001g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.940+5511A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950786 | |||||||
chr4:109950805 | C | T | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.940+5530C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109950805 | |||||||
chr4:109951034 | C | T | 5 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0006c0006t0001g0009 others(2): Show |
6 | HG02615.hp2 HG02630.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+5759C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951034 | |||||||
chr4:109951146 | A | AAAAAT | 69 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(66): Show |
72 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.940+5922_940+5926d others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | A | AAAAATAA others(3): Show |
15 | a0001c0001t0002g0070 a0001c0001t0002g0125 a0001c0001t0002g0308 others(12): Show |
17 | HG00323.hp2 HG01074.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.940+5917_940+5926d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | A | AAAAATAA others(8): Show |
9 | a0001c0001t0002g0124 a0001c0001t0007g0118 a0001c0001t0007g0121 others(6): Show |
9 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.940+5912_940+5926d others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | A | AAAAATAA others(13): Show |
2 | a0001c0001t0011g0143 a0001c0001t0028g0237 |
2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.940+5907_940+5926d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | A | AAAAATAA others(18): Show |
1 | a0001c0001t0002g0123 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.940+5902_940+5926d others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | AAAAAT | A | 118 | a0001c0001t0002g0092 a0001c0001t0002g0115 a0001c0001t0004g0024 others(115): Show |
120 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.940+5922_940+5926d others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | AAAAATAA others(3): Show |
A | 59 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(56): Show |
60 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.940+5917_940+5926d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | AAAAATAA others(8): Show |
A | 7 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0002c0002t0001g0131 others(4): Show |
7 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.940+5912_940+5926d others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951146 | AAAAATAA others(18): Show |
A | 1 | a0003c0003t0005g0030 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.940+5902_940+5926d others(27): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951146 | ||||||
chr4:109951176 | T | C | 1 | a0009c0010t0016g0352 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.940+5901T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951176 | |||||||
chr4:109951247 | A | G | 3 | a0004c0004t0003g0264 a0004c0004t0010g0255 a0005c0005t0004g0301 |
3 | HG02129.hp2 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.940+5972A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951247 | |||||||
chr4:109951403 | G | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+6128G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951403 | |||||||
chr4:109951470 | GT | G | 6 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(3): Show |
7 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+6202delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109951470 | ||||||
chr4:109951960 | A | G | 5 | a0005c0005t0019g0012 a0005c0005t0019g0243 a0005c0005t0019g0246 others(2): Show |
6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+6685A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109951960 | |||||||
chr4:109952575 | G | A | 4 | a0002c0002t0001g0008 a0002c0002t0001g0151 a0002c0002t0001g0155 others(1): Show |
5 | NA18941.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.941-6737G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952575 | |||||||
chr4:109952575 | G | T | 1 | a0001c0027t0004g0326 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.941-6737G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952575 | |||||||
chr4:109952596 | A | G | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-6716A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952596 | |||||||
chr4:109952601 | A | G | 77 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(74): Show |
80 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.941-6711A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952601 | |||||||
chr4:109952623 | T | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-6689T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952623 | |||||||
chr4:109952630 | A | T | 1 | a0010c0011t0001g0199 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.941-6682A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952630 | |||||||
chr4:109952638 | C | A | 1 | a0005c0005t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.941-6674C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952638 | |||||||
chr4:109952770 | T | C | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.941-6542T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952770 | |||||||
chr4:109952910 | G | C | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-6402G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952910 | |||||||
chr4:109952954 | T | C | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-6358T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109952954 | |||||||
chr4:109953141 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.941-6171G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953141 | |||||||
chr4:109953217 | T | C | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.941-6095T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953217 | |||||||
chr4:109953513 | C | A | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.941-5799C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953513 | |||||||
chr4:109953513 | C | T | 1 | a0002c0002t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.941-5799C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953513 | |||||||
chr4:109953554 | A | C | 2 | a0001c0016t0002g0051 a0001c0016t0006g0029 |
2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.941-5758A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953554 | |||||||
chr4:109953617 | A | T | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941-5695A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953617 | |||||||
chr4:109953869 | G | A | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.941-5443G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953869 | |||||||
chr4:109953957 | C | T | 55 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(52): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.941-5355C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109953957 | |||||||
chr4:109954052 | T | C | 2 | a0008c0009t0001g0060 a0008c0009t0001g0061 |
2 | NA18970.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.941-5260T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954052 | |||||||
chr4:109954074 | C | T | 1 | a0005c0005t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.941-5238C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954074 | |||||||
chr4:109954106 | C | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-5206C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954106 | |||||||
chr4:109954124 | TCACTGCA others(1): Show |
T | 3 | a0004c0004t0003g0264 a0004c0004t0010g0255 a0005c0005t0004g0301 |
3 | HG02129.hp2 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.941-5186_941-5179d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109954124 | ||||||
chr4:109954194 | G | A | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-5118G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954194 | |||||||
chr4:109954222 | T | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.941-5090T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954222 | |||||||
chr4:109954434 | C | G | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.941-4878C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954434 | |||||||
chr4:109954505 | C | T | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.941-4807C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954505 | |||||||
chr4:109954663 | C | T | 7 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-4649C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954663 | |||||||
chr4:109954761 | G | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.941-4551G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954761 | |||||||
chr4:109954968 | G | A | 4 | a0001c0001t0012g0372 a0001c0001t0014g0229 a0001c0001t0015g0371 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-4344G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109954968 | |||||||
chr4:109955086 | G | T | 1 | a0001c0001t0025g0097 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.941-4226G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955086 | |||||||
chr4:109955152 | T | G | 1 | a0001c0001t0006g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.941-4160T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955152 | |||||||
chr4:109955253 | G | T | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.941-4059G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955253 | |||||||
chr4:109955574 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.941-3738G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955574 | |||||||
chr4:109955611 | G | A | 1 | a0002c0002t0001g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.941-3701G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955611 | |||||||
chr4:109955792 | C | T | 1 | a0010c0011t0001g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.941-3520C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955792 | |||||||
chr4:109955796 | G | A | 1 | a0001c0001t0015g0373 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.941-3516G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955796 | |||||||
chr4:109955891 | G | A | 4 | a0001c0001t0012g0232 a0001c0001t0020g0011 a0001c0001t0020g0230 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-3421G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109955891 | |||||||
chr4:109956187 | A | T | 53 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(50): Show |
54 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.941-3125A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956187 | |||||||
chr4:109956260 | A | T | 138 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(135): Show |
141 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.941-3052A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956260 | |||||||
chr4:109956364 | C | T | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-2948C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956364 | |||||||
chr4:109956822 | G | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-2490G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109956822 | |||||||
chr4:109957109 | C | G | 1 | a0005c0005t0007g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.941-2203C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109957109 | |||||||
chr4:109957413 | A | C | 1 | a0002c0002t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.941-1899A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109957413 | |||||||
chr4:109957659 | C | G | 1 | a0001c0001t0004g0325 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.941-1653C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109957659 | |||||||
chr4:109958135 | C | T | 4 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0018 others(1): Show |
4 | HG02818.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-1177C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958135 | |||||||
chr4:109958144 | A | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.941-1168A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958144 | |||||||
chr4:109958190 | G | A | 8 | a0003c0003t0005g0027 a0003c0003t0005g0030 a0003c0003t0005g0039 others(5): Show |
8 | HG00609.hp2 HG02027.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-1122G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958190 | |||||||
chr4:109958299 | C | T | 1 | a0007c0008t0032g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.941-1013C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958299 | |||||||
chr4:109958328 | T | C | 3 | a0001c0001t0004g0328 a0001c0001t0004g0334 a0001c0001t0013g0348 |
3 | NA18957.hp2 NA18998.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.941-984T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958328 | |||||||
chr4:109958566 | T | C | 1 | a0001c0001t0029g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.941-746T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958566 | |||||||
chr4:109958725 | C | T | 5 | a0005c0005t0019g0012 a0005c0005t0019g0243 a0005c0005t0019g0246 others(2): Show |
6 | HG01255.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.941-587C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958725 | |||||||
chr4:109958747 | G | A | 7 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-565G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958747 | |||||||
chr4:109958883 | A | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.941-429A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958883 | |||||||
chr4:109958900 | A | G | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941-412A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109958900 | |||||||
chr4:109958917 | C | CA | 28 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(25): Show |
30 | HG00140.hp2 HG01081.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.941-374dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109958917 | ||||||
chr4:109958917 | CA | C | 138 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(135): Show |
142 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.941-374delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109958917 | ||||||
chr4:109958917 | CAA | C | 63 | a0001c0001t0002g0075 a0001c0001t0004g0291 a0001c0001t0004g0292 others(60): Show |
63 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.941-375_941-374del others(2): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 109958917 | ||||||
chr4:109959002 | C | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.941-310C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959002 | |||||||
chr4:109959190 | C | T | 1 | a0003c0003t0005g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.941-122C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959190 | |||||||
chr4:109959206 | T | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.941-106T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959206 | |||||||
chr4:109959208 | T | C | 191 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(188): Show |
195 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.941-104T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959208 | |||||||
chr4:109959222 | A | C | 5 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-90A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 5/23 | chr4 | 109959222 | |||||||
chr4:109959418 | A | AGACCGGA others(41): Show |
1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1049_1066+30dupACC others(45): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr4 | 109959418 | ||||||
chr4:109959447 | G | C | 2 | a0003c0003t0005g0054 a0003c0003t0008g0059 |
2 | NA18947.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1066+10G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959447 | |||||||
chr4:109959477 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1066+40C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959477 | |||||||
chr4:109959631 | C | T | 3 | a0001c0001t0004g0328 a0001c0001t0004g0334 a0001c0001t0013g0348 |
3 | NA18957.hp2 NA18998.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1066+194C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959631 | |||||||
chr4:109959982 | A | G | 1 | a0002c0002t0001g0157 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1066+545A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109959982 | |||||||
chr4:109960002 | G | A | 1 | a0001c0001t0020g0230 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1066+565G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960002 | |||||||
chr4:109960208 | G | A | 1 | a0002c0002t0006g0005 | 2 | HG01074.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1067-659G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960208 | |||||||
chr4:109960210 | T | G | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1067-657T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960210 | |||||||
chr4:109960338 | A | G | 149 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(146): Show |
153 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1067-529A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960338 | |||||||
chr4:109960456 | G | A | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1067-411G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960456 | |||||||
chr4:109960645 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1067-222G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960645 | |||||||
chr4:109960746 | C | T | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1067-121C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 6/23 | chr4 | 109960746 | |||||||
chr4:109961304 | G | A | 77 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(74): Show |
80 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.1189+315G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961304 | |||||||
chr4:109961309 | C | G | 7 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189+320C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961309 | |||||||
chr4:109961320 | C | A | 197 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(194): Show |
202 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1189+331C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961320 | |||||||
chr4:109961434 | A | G | 149 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(146): Show |
153 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1190-429A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961434 | |||||||
chr4:109961753 | C | A | 1 | a0002c0002t0001g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1190-110C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961753 | |||||||
chr4:109961824 | G | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1190-39G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961824 | |||||||
chr4:109961840 | T | C | 65 | a0001c0001t0004g0120 a0001c0001t0004g0291 a0001c0001t0004g0292 others(62): Show |
66 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1190-23T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 7/23 | chr4 | 109961840 | |||||||
chr4:109962008 | C | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1312+23C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962008 | |||||||
chr4:109962185 | T | G | 10 | a0001c0001t0015g0175 a0002c0002t0001g0174 a0002c0002t0001g0176 others(7): Show |
10 | HG02165.hp2 HG03704.hp1 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312+200T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962185 | |||||||
chr4:109962188 | C | T | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1312+203C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962188 | |||||||
chr4:109962449 | A | G | 4 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(1): Show |
5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312+464A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962449 | |||||||
chr4:109962464 | G | A | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1312+479G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962464 | |||||||
chr4:109962580 | T | C | 1 | a0007c0008t0003g0369 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1313-593T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962580 | |||||||
chr4:109962731 | C | T | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-442C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962731 | |||||||
chr4:109962896 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1313-277G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962896 | |||||||
chr4:109962998 | C | A | 10 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(7): Show |
11 | HG02615.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1313-175C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109962998 | |||||||
chr4:109963064 | C | CA | 7 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(4): Show |
8 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1313-92dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 109963064 | ||||||
chr4:109963064 | C | CAA | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-93_1313-92dup others(2): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 109963064 | ||||||
chr4:109963064 | CA | C | 64 | a0001c0001t0002g0106 a0001c0001t0002g0310 a0001c0001t0006g0249 others(61): Show |
65 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.1313-92delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 109963064 | ||||||
chr4:109963140 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1313-33C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109963140 | |||||||
chr4:109963163 | G | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01192.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1313-10G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 8/23 | chr4 | 109963163 | |||||||
chr4:109963401 | G | A | 7 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1438+103G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963401 | |||||||
chr4:109963587 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1438+289T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963587 | |||||||
chr4:109963589 | T | C | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1438+291T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963589 | |||||||
chr4:109963612 | A | G | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1438+314A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963612 | |||||||
chr4:109963785 | A | G | 3 | a0002c0002t0023g0220 a0002c0002t0023g0222 a0002c0002t0036g0221 |
3 | HG02280.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1438+487A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963785 | |||||||
chr4:109963830 | A | T | 11 | a0005c0005t0007g0001 a0005c0005t0007g0241 a0005c0005t0007g0275 others(8): Show |
12 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1438+532A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963830 | |||||||
chr4:109963896 | A | G | 1 | a0002c0002t0035g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1439-505A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963896 | |||||||
chr4:109963988 | C | T | 1 | a0002c0002t0036g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1439-413C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109963988 | |||||||
chr4:109964086 | A | T | 149 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(146): Show |
153 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1439-315A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109964086 | |||||||
chr4:109964188 | G | A | 1 | a0006c0006t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1439-213G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 9/23 | chr4 | 109964188 | |||||||
chr4:109964554 | T | C | 1 | a0002c0002t0001g0174 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1575+17T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964554 | |||||||
chr4:109964587 | A | G | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+50A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964587 | |||||||
chr4:109964626 | A | T | 1 | a0007c0008t0003g0369 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1575+89A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964626 | |||||||
chr4:109964656 | A | G | 1 | a0002c0002t0009g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1575+119A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964656 | |||||||
chr4:109964712 | T | C | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
282 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1575+175T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964712 | |||||||
chr4:109964773 | C | T | 1 | a0002c0002t0001g0306 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1575+236C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964773 | |||||||
chr4:109964801 | G | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1575+264G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964801 | |||||||
chr4:109964993 | C | T | 58 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0004c0004t0003g0013 others(55): Show |
60 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+456C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109964993 | |||||||
chr4:109965029 | G | A | 1 | a0005c0005t0006g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1575+492G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965029 | |||||||
chr4:109965098 | G | C | 1 | a0001c0001t0015g0371 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1575+561G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965098 | |||||||
chr4:109965150 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1575+613G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965150 | |||||||
chr4:109965187 | G | C | 269 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(266): Show |
277 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1575+650G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965187 | |||||||
chr4:109965341 | C | A | 10 | a0001c0001t0002g0104 a0001c0001t0002g0106 a0001c0001t0002g0108 others(7): Show |
10 | HG02523.hp2 NA18945.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+804C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965341 | |||||||
chr4:109965648 | T | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(73): Show |
79 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1575+1111T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965648 | |||||||
chr4:109965884 | T | C | 1 | a0001c0001t0015g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1575+1347T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109965884 | |||||||
chr4:109966036 | A | AAT | 53 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(50): Show |
55 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.1575+1500_1575+150 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109966036 | ||||||
chr4:109966036 | A | AATAT | 4 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0005c0005t0006g0245 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1575+1500_1575+150 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109966036 | ||||||
chr4:109966037 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1575+1500A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966037 | |||||||
chr4:109966038 | A | T | 58 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0004c0004t0003g0013 others(55): Show |
60 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+1501A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966038 | |||||||
chr4:109966040 | T | A | 18 | a0001c0001t0006g0249 a0001c0001t0011g0142 a0001c0001t0011g0143 others(15): Show |
18 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1575+1503T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966040 | |||||||
chr4:109966076 | A | G | 1 | a0001c0001t0029g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1575+1539A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966076 | |||||||
chr4:109966098 | T | C | 55 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(52): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1575+1561T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966098 | |||||||
chr4:109966299 | A | G | 1 | a0002c0002t0035g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1575+1762A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966299 | |||||||
chr4:109966470 | G | T | 1 | a0002c0002t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1575+1933G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966470 | |||||||
chr4:109966505 | C | T | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1575+1968C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966505 | |||||||
chr4:109966673 | G | A | 58 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0004c0004t0003g0013 others(55): Show |
60 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1575+2136G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966673 | |||||||
chr4:109966833 | G | A | 275 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(272): Show |
283 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1576-2138G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109966833 | |||||||
chr4:109967310 | A | G | 1 | a0005c0005t0019g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1576-1661A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967310 | |||||||
chr4:109967311 | C | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-1660C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967311 | |||||||
chr4:109967352 | G | A | 1 | a0002c0002t0009g0150 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1576-1619G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967352 | |||||||
chr4:109967371 | G | C | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1576-1600G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967371 | |||||||
chr4:109967473 | G | A | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1576-1498G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967473 | |||||||
chr4:109967699 | C | T | 3 | a0001c0001t0029g0238 a0019c0034t0020g0370 a0022c0035t0017g0126 |
3 | HG02559.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1576-1272C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967699 | |||||||
chr4:109967848 | A | G | 1 | a0004c0004t0010g0272 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1576-1123A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967848 | |||||||
chr4:109967851 | A | C | 73 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(70): Show |
76 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.1576-1120A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967851 | |||||||
chr4:109967855 | A | C | 1 | a0001c0001t0006g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1576-1116A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109967855 | |||||||
chr4:109968118 | A | G | 4 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0001c0001t0033g0231 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-853A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968118 | |||||||
chr4:109968145 | G | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1576-826G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968145 | |||||||
chr4:109968280 | T | G | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-691T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968280 | |||||||
chr4:109968553 | A | G | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1576-418A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968553 | |||||||
chr4:109968557 | A | G | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1576-414A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968557 | |||||||
chr4:109968673 | C | CATCT | 14 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0001t0011g0147 others(11): Show |
14 | HG01109.hp2 HG01169.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1576-264_1576-261d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968673 | C | CATCTATC others(1): Show |
41 | a0001c0001t0002g0076 a0001c0001t0002g0093 a0001c0001t0002g0104 others(38): Show |
41 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1576-268_1576-261d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968673 | C | CATCTATC others(5): Show |
94 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0069 others(91): Show |
95 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1576-272_1576-261d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968673 | C | CATCTATC others(9): Show |
39 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0071 others(36): Show |
42 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1576-276_1576-261d others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968673 | C | CATCTATC others(13): Show |
20 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0084 others(17): Show |
21 | HG00597.hp2 HG00609.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1576-280_1576-261d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968673 | CATCT | C | 89 | a0001c0001t0006g0249 a0001c0001t0012g0212 a0001c0001t0012g0214 others(86): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1576-264_1576-261d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968673 | CATCTATC others(1): Show |
C | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0189 |
3 | NA18969.hp1 NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1576-268_1576-261d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968673 | ||||||
chr4:109968676 | C | CTATCTAT others(1): Show |
5 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(2): Show |
6 | HG02647.hp1 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-288_1576-287i others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968676 | ||||||
chr4:109968699 | T | TCTACCTA others(5): Show |
13 | a0003c0003t0005g0003 a0003c0003t0005g0019 a0003c0003t0005g0026 others(10): Show |
14 | HG00609.hp2 HG02015.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1576-269_1576-268i others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968699 | ||||||
chr4:109968703 | T | C | 13 | a0003c0003t0005g0003 a0003c0003t0005g0019 a0003c0003t0005g0026 others(10): Show |
14 | HG00609.hp2 HG02015.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1576-268T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968703 | |||||||
chr4:109968703 | T | TCTACCTA others(9): Show |
26 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(23): Show |
26 | HG00423.hp1 HG02027.hp1 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1576-265_1576-264i others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968703 | ||||||
chr4:109968707 | T | C | 39 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(36): Show |
40 | HG00423.hp1 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.1576-264T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968707 | |||||||
chr4:109968707 | T | TCTACCTA others(5): Show |
10 | a0004c0004t0010g0255 a0004c0032t0003g0262 a0005c0005t0006g0245 others(7): Show |
11 | HG01255.hp1 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1576-252_1576-241d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | ||||||
chr4:109968707 | T | TCTACCTA others(9): Show |
41 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0004c0004t0003g0013 others(38): Show |
42 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1576-256_1576-241d others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | ||||||
chr4:109968707 | T | TCTACCTA others(13): Show |
15 | a0003c0003t0005g0054 a0003c0003t0008g0034 a0003c0003t0008g0042 others(12): Show |
15 | HG00621.hp1 HG01109.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1576-260_1576-241d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | ||||||
chr4:109968707 | T | TCTACCTA others(17): Show |
1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1576-241_1576-240i others(26): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | ||||||
chr4:109968707 | T | TCTATCTA others(5): Show |
1 | a0001c0001t0015g0371 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1576-261_1576-260i others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | ||||||
chr4:109968707 | T | TCTATCTA others(13): Show |
1 | a0001c0001t0004g0332 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1576-261_1576-260i others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968707 | ||||||
chr4:109968711 | C | T | 7 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0115 others(4): Show |
7 | NA18942.hp1 NA18946.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-260C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968711 | |||||||
chr4:109968753 | T | C | 106 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(103): Show |
109 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1576-218T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968753 | |||||||
chr4:109968779 | T | A | 47 | a0001c0001t0004g0316 a0001c0001t0004g0320 a0001c0001t0004g0321 others(44): Show |
47 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-192T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968779 | |||||||
chr4:109968860 | C | T | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-111C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968860 | |||||||
chr4:109968887 | T | C | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1576-84T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968887 | |||||||
chr4:109968933 | T | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-38T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | chr4 | 109968933 | |||||||
chr4:109968933 | TA | T | 49 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1576-29delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 109968933 | ||||||
chr4:109969310 | C | T | 4 | a0002c0002t0001g0010 a0002c0002t0001g0197 a0002c0002t0001g0198 others(1): Show |
5 | HG00597.hp1 HG02040.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724+191C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969310 | |||||||
chr4:109969373 | T | A | 7 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724+254T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969373 | |||||||
chr4:109969381 | C | T | 6 | a0001c0001t0004g0327 a0001c0001t0004g0328 a0001c0001t0004g0334 others(3): Show |
6 | HG00438.hp2 NA18957.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1724+262C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969381 | |||||||
chr4:109969548 | T | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1724+429T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969548 | |||||||
chr4:109969606 | A | C | 2 | a0019c0034t0020g0370 a0022c0035t0017g0126 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1724+487A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969606 | |||||||
chr4:109969744 | T | C | 46 | a0001c0001t0004g0024 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1724+625T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969744 | |||||||
chr4:109969780 | C | A | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1724+661C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969780 | |||||||
chr4:109969832 | A | C | 1 | a0004c0004t0003g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1724+713A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109969832 | |||||||
chr4:109970168 | G | A | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1724+1049G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970168 | |||||||
chr4:109970186 | T | A | 4 | a0004c0004t0003g0258 a0004c0004t0003g0259 a0004c0004t0003g0281 others(1): Show |
4 | NA18954.hp1 NA18965.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1724+1067T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970186 | |||||||
chr4:109970387 | A | C | 155 | a0001c0001t0004g0024 a0001c0001t0004g0316 a0001c0001t0004g0320 others(152): Show |
158 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.1724+1268A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970387 | |||||||
chr4:109970517 | T | C | 277 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(274): Show |
284 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1724+1398T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970517 | |||||||
chr4:109970602 | A | G | 1 | a0002c0002t0001g0160 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1724+1483A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970602 | |||||||
chr4:109970617 | G | A | 1 | a0002c0002t0036g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1724+1498G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970617 | |||||||
chr4:109970622 | C | G | 9 | a0001c0001t0006g0249 a0001c0001t0012g0232 a0001c0001t0020g0011 others(6): Show |
9 | HG01884.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1724+1503C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970622 | |||||||
chr4:109970629 | A | C | 2 | a0015c0018t0017g0063 a0015c0018t0017g0134 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1724+1510A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970629 | |||||||
chr4:109970629 | A | G | 3 | a0004c0004t0003g0302 a0004c0004t0010g0062 a0005c0005t0013g0256 |
3 | NA18956.hp1 NA18978.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1724+1510A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970629 | |||||||
chr4:109970631 | C | T | 1 | a0002c0002t0036g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1724+1512C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970631 | |||||||
chr4:109970639 | A | G | 1 | a0002c0002t0009g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1724+1520A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970639 | |||||||
chr4:109970642 | T | C | 7 | a0001c0001t0006g0249 a0002c0002t0001g0130 a0002c0002t0009g0205 others(4): Show |
7 | HG02809.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1724+1523T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970642 | |||||||
chr4:109970643 | G | A | 1 | a0004c0004t0003g0242 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1724+1524G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970643 | |||||||
chr4:109970653 | C | T | 136 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0004g0024 others(133): Show |
140 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1724+1534C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970653 | |||||||
chr4:109970686 | C | A | 1 | a0003c0003t0008g0045 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1724+1567C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970686 | |||||||
chr4:109970703 | T | C | 4 | a0001c0001t0002g0078 a0001c0001t0003g0077 a0001c0001t0003g0079 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1724+1584T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970703 | |||||||
chr4:109970742 | G | T | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1724+1623G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970742 | |||||||
chr4:109970749 | T | C | 1 | a0001c0001t0011g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1724+1630T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970749 | |||||||
chr4:109970752 | A | G | 1 | a0001c0001t0011g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1724+1633A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970752 | |||||||
chr4:109970773 | G | C | 2 | a0004c0004t0010g0272 a0016c0030t0016g0305 |
2 | HG00738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1724+1654G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970773 | |||||||
chr4:109970780 | G | A | 2 | a0001c0007t0002g0006 a0001c0007t0002g0103 |
3 | HG01515.hp1 HG01517.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1724+1661G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970780 | |||||||
chr4:109970812 | G | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1724+1693G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970812 | |||||||
chr4:109970824 | C | CA | 86 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(83): Show |
89 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1724+1727dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAA | 10 | a0001c0001t0002g0069 a0001c0001t0002g0092 a0001c0001t0002g0108 others(7): Show |
10 | HG02486.hp1 HG02615.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1724+1726_1724+172 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(1): Show |
41 | a0004c0004t0003g0013 a0004c0004t0003g0127 a0004c0004t0003g0242 others(38): Show |
42 | HG00558.hp1 HG00597.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1724+1720_1724+172 others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(2): Show |
58 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(55): Show |
60 | HG00621.hp1 HG01109.hp2 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.1724+1719_1724+172 others(13): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(3): Show |
21 | a0001c0001t0011g0143 a0001c0019t0017g0141 a0003c0003t0005g0032 others(18): Show |
21 | HG00423.hp1 HG00609.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1724+1718_1724+172 others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(4): Show |
1 | a0001c0019t0007g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1724+1717_1724+172 others(15): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(6): Show |
3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 |
3 | HG02559.hp2 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1724+1715_1724+172 others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0022g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1724+1713_1724+172 others(19): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0022g0239 a0001c0001t0028g0237 a0001c0001t0029g0238 |
3 | HG00735.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1724+1712_1724+172 others(20): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970824 | CA | C | 13 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(10): Show |
13 | HG01070.hp2 HG01891.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1724+1727delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109970824 | ||||||
chr4:109970856 | T | G | 283 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(280): Show |
291 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.1724+1737T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109970856 | |||||||
chr4:109971007 | T | C | 274 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(271): Show |
281 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.1724+1888T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971007 | |||||||
chr4:109971416 | C | T | 47 | a0001c0001t0004g0332 a0001c0016t0002g0051 a0001c0016t0006g0029 others(44): Show |
48 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1724+2297C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971416 | |||||||
chr4:109971469 | G | A | 67 | a0001c0001t0007g0312 a0004c0004t0003g0013 a0004c0004t0003g0127 others(64): Show |
69 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1724+2350G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971469 | |||||||
chr4:109971499 | G | A | 12 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(9): Show |
12 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1724+2380G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971499 | |||||||
chr4:109971578 | C | A | 1 | a0002c0002t0035g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1724+2459C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109971578 | |||||||
chr4:109972031 | A | C | 1 | a0001c0001t0004g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1725-2672A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972031 | |||||||
chr4:109972045 | TA | T | 7 | a0008c0009t0001g0060 a0008c0009t0001g0061 a0008c0009t0001g0184 others(4): Show |
7 | NA18946.hp1 NA18950.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1725-2647delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109972045 | ||||||
chr4:109972056 | A | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1725-2647A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972056 | |||||||
chr4:109972408 | CGAAACAG others(13): Show |
C | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1725-2294_1725-227 others(24): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972408 | |||||||
chr4:109972434 | C | T | 1 | a0001c0019t0017g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1725-2269C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972434 | |||||||
chr4:109972463 | T | G | 49 | a0001c0001t0004g0332 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1725-2240T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972463 | |||||||
chr4:109972681 | G | T | 5 | a0001c0001t0015g0175 a0002c0002t0001g0174 a0002c0002t0001g0176 others(2): Show |
5 | HG02165.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-2022G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972681 | |||||||
chr4:109972821 | A | C | 47 | a0001c0001t0004g0332 a0001c0016t0002g0051 a0001c0016t0006g0029 others(44): Show |
48 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1725-1882A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972821 | |||||||
chr4:109972836 | A | G | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1867A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109972836 | |||||||
chr4:109973127 | C | T | 1 | a0002c0002t0006g0351 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1725-1576C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973127 | |||||||
chr4:109973145 | C | T | 68 | a0001c0001t0006g0249 a0001c0001t0007g0312 a0004c0004t0003g0013 others(65): Show |
70 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1725-1558C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973145 | |||||||
chr4:109973196 | G | A | 2 | a0003c0003t0005g0037 a0003c0003t0008g0033 |
2 | NA18995.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1725-1507G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973196 | |||||||
chr4:109973246 | C | G | 46 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1725-1457C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973246 | |||||||
chr4:109973293 | A | G | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
75 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1725-1410A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973293 | |||||||
chr4:109973324 | C | A | 1 | a0003c0003t0008g0047 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1725-1379C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973324 | |||||||
chr4:109973329 | A | C | 3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0022c0035t0017g0126 |
3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1725-1374A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973329 | |||||||
chr4:109973366 | C | T | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1337C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973366 | |||||||
chr4:109973470 | T | C | 3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0022c0035t0017g0126 |
3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1725-1233T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973470 | |||||||
chr4:109973475 | G | C | 1 | a0002c0002t0001g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1725-1228G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973475 | |||||||
chr4:109973488 | A | G | 1 | a0003c0003t0005g0049 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1725-1215A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973488 | |||||||
chr4:109973529 | A | C | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725-1174A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973529 | |||||||
chr4:109973594 | A | G | 1 | a0001c0001t0007g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1725-1109A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973594 | |||||||
chr4:109973626 | T | TCC | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725-1076_1725-107 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr4 | 109973626 | ||||||
chr4:109973710 | G | T | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1725-993G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973710 | |||||||
chr4:109973902 | T | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1725-801T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973902 | |||||||
chr4:109973957 | G | A | 267 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(264): Show |
274 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.1725-746G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109973957 | |||||||
chr4:109974102 | A | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1725-601A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109974102 | |||||||
chr4:109974277 | A | G | 12 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(9): Show |
12 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1725-426A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109974277 | |||||||
chr4:109974691 | C | A | 48 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0001c0019t0007g0140 others(45): Show |
49 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1725-12C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 11/23 | chr4 | 109974691 | |||||||
chr4:109974894 | A | C | 63 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(60): Show |
65 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1829+87A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109974894 | |||||||
chr4:109974932 | A | T | 1 | a0008c0009t0001g0185 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1829+125A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109974932 | |||||||
chr4:109975078 | T | C | 1 | a0002c0002t0001g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1829+271T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975078 | |||||||
chr4:109975334 | C | T | 1 | a0001c0001t0014g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1829+527C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975334 | |||||||
chr4:109975446 | C | A | 48 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0001c0019t0007g0140 others(45): Show |
49 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1830-566C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975446 | |||||||
chr4:109975731 | T | G | 150 | a0001c0001t0004g0120 a0001c0001t0006g0249 a0001c0001t0007g0007 others(147): Show |
154 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.1830-281T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 12/23 | chr4 | 109975731 | |||||||
chr4:109976379 | G | A | 72 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(69): Show |
75 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.2053+144G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109976379 | |||||||
chr4:109976429 | G | A | 6 | a0006c0006t0009g0159 a0012c0014t0007g0135 a0012c0014t0007g0138 others(3): Show |
6 | HG02257.hp1 HG02486.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2053+194G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109976429 | |||||||
chr4:109976808 | T | G | 3 | a0003c0003t0005g0030 a0003c0003t0005g0039 a0003c0003t0005g0040 |
3 | NA18939.hp1 NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2053+573T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109976808 | |||||||
chr4:109977100 | A | G | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2053+865A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977100 | |||||||
chr4:109977139 | A | G | 2 | a0002c0002t0001g0202 a0002c0002t0001g0203 |
2 | HG04184.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2053+904A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977139 | |||||||
chr4:109977273 | T | C | 8 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(5): Show |
8 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2053+1038T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977273 | |||||||
chr4:109977536 | TA | T | 10 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(7): Show |
11 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2053+1314delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 109977536 | ||||||
chr4:109977659 | C | A | 46 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2053+1424C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977659 | |||||||
chr4:109977769 | T | G | 148 | a0001c0001t0004g0120 a0001c0001t0006g0249 a0001c0001t0007g0007 others(145): Show |
152 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.2053+1534T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977769 | |||||||
chr4:109977833 | G | A | 3 | a0001c0019t0007g0140 a0001c0019t0017g0141 a0002c0002t0001g0192 |
3 | HG02615.hp2 HG02630.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2053+1598G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977833 | |||||||
chr4:109977880 | A | G | 1 | a0005c0005t0007g0275 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2053+1645A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977880 | |||||||
chr4:109977933 | C | G | 1 | a0002c0002t0009g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2053+1698C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109977933 | |||||||
chr4:109978074 | T | G | 2 | a0001c0001t0004g0360 a0001c0001t0004g0362 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2053+1839T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109978074 | |||||||
chr4:109978237 | T | C | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2054-1735T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109978237 | |||||||
chr4:109978752 | G | A | 46 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2054-1220G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109978752 | |||||||
chr4:109979057 | C | T | 1 | a0001c0001t0004g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2054-915C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979057 | |||||||
chr4:109979081 | C | A | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2054-891C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979081 | |||||||
chr4:109979187 | A | G | 10 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(7): Show |
11 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2054-785A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979187 | |||||||
chr4:109979289 | T | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2054-683T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979289 | |||||||
chr4:109979357 | C | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2054-615C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979357 | |||||||
chr4:109979444 | G | A | 20 | a0001c0001t0006g0249 a0001c0001t0007g0312 a0005c0005t0006g0245 others(17): Show |
21 | HG01109.hp2 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.2054-528G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979444 | |||||||
chr4:109979450 | G | A | 3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0022c0035t0017g0126 |
3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2054-522G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979450 | |||||||
chr4:109979536 | G | C | 270 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(267): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2054-436G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979536 | |||||||
chr4:109979635 | G | A | 270 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(267): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2054-337G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979635 | |||||||
chr4:109979662 | A | G | 41 | a0001c0001t0004g0024 a0001c0001t0004g0316 a0001c0001t0004g0320 others(38): Show |
41 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.2054-310A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979662 | |||||||
chr4:109979861 | A | G | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2054-111A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979861 | |||||||
chr4:109979879 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2054-93A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 13/23 | chr4 | 109979879 | |||||||
chr4:109980221 | G | T | 1 | a0003c0003t0008g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2221+82G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980221 | |||||||
chr4:109980264 | G | T | 9 | a0005c0005t0011g0342 a0009c0010t0016g0344 a0009c0010t0016g0345 others(6): Show |
9 | HG01109.hp2 HG01975.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2221+125G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980264 | |||||||
chr4:109980285 | A | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2221+146A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980285 | |||||||
chr4:109980418 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0066 |
2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2221+279G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980418 | |||||||
chr4:109980464 | G | A | 3 | a0002c0002t0023g0220 a0002c0002t0023g0222 a0002c0002t0036g0221 |
3 | HG02280.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2221+325G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980464 | |||||||
chr4:109980497 | T | C | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2222-329T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980497 | |||||||
chr4:109980532 | G | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2222-294G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980532 | |||||||
chr4:109980701 | A | G | 5 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0016c0030t0016g0305 others(2): Show |
5 | HG00738.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2222-125A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980701 | |||||||
chr4:109980741 | C | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2222-85C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 14/23 | chr4 | 109980741 | |||||||
chr4:109980994 | T | A | 1 | a0001c0007t0002g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2371+19T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109980994 | |||||||
chr4:109981010 | G | A | 3 | a0004c0004t0003g0252 a0004c0004t0003g0253 a0004c0004t0003g0277 |
3 | HG01928.hp2 HG01978.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2371+35G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981010 | |||||||
chr4:109981345 | T | G | 1 | a0001c0001t0044g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2371+370T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981345 | |||||||
chr4:109981528 | T | C | 8 | a0001c0001t0002g0065 a0001c0007t0002g0006 a0001c0007t0002g0100 others(5): Show |
9 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.2371+553T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981528 | |||||||
chr4:109981543 | T | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2371+568T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981543 | |||||||
chr4:109981578 | T | A | 46 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2371+603T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981578 | |||||||
chr4:109981686 | A | T | 2 | a0003c0003t0005g0039 a0003c0003t0005g0040 |
2 | NA18939.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2371+711A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981686 | |||||||
chr4:109981856 | C | G | 79 | a0001c0001t0006g0249 a0001c0001t0007g0312 a0001c0001t0011g0142 others(76): Show |
81 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2371+881C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981856 | |||||||
chr4:109981913 | A | G | 66 | a0001c0001t0006g0249 a0001c0001t0007g0312 a0004c0004t0003g0013 others(63): Show |
68 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(65): Show |
intron_variant | MODIFIER | c.2371+938A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109981913 | |||||||
chr4:109982070 | G | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0018 others(2): Show |
5 | HG02818.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2371+1095G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982070 | |||||||
chr4:109982078 | G | C | 3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0022c0035t0017g0126 |
3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2371+1103G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982078 | |||||||
chr4:109982223 | G | T | 1 | a0001c0001t0006g0099 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2372-1199G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982223 | |||||||
chr4:109982387 | G | T | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2372-1035G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982387 | |||||||
chr4:109982418 | C | G | 8 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0115 others(5): Show |
8 | NA18942.hp1 NA18946.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.2372-1004C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982418 | |||||||
chr4:109982460 | T | C | 51 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(48): Show |
52 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2372-962T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982460 | |||||||
chr4:109982629 | TTTTTC | T | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372-773_2372-769d others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 109982629 | ||||||
chr4:109982629 | TTTTTCTT others(3): Show |
T | 4 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0028g0237 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372-778_2372-769d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 109982629 | ||||||
chr4:109982658 | T | C | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372-764T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982658 | |||||||
chr4:109982697 | G | A | 2 | a0001c0001t0011g0142 a0001c0001t0011g0145 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2372-725G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982697 | |||||||
chr4:109982821 | G | T | 2 | a0008c0009t0001g0187 a0008c0009t0001g0188 |
2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2372-601G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109982821 | |||||||
chr4:109983095 | C | T | 4 | a0004c0004t0003g0283 a0004c0004t0003g0284 a0004c0004t0003g0285 others(1): Show |
4 | HG01175.hp1 HG02148.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372-327C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983095 | |||||||
chr4:109983098 | G | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2372-324G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983098 | |||||||
chr4:109983216 | T | C | 1 | a0001c0001t0006g0311 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2372-206T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983216 | |||||||
chr4:109983288 | G | A | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2372-134G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983288 | |||||||
chr4:109983292 | C | T | 270 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(267): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2372-130C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983292 | |||||||
chr4:109983334 | C | T | 3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0022c0035t0017g0126 |
3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2372-88C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983334 | |||||||
chr4:109983346 | G | A | 194 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(191): Show |
198 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.2372-76G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 15/23 | chr4 | 109983346 | |||||||
chr4:109983561 | C | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+20C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109983561 | |||||||
chr4:109983817 | C | T | 267 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(264): Show |
274 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.2491+276C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109983817 | |||||||
chr4:109984141 | C | A | 2 | a0006c0006t0001g0298 a0006c0006t0001g0299 |
2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2491+600C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984141 | |||||||
chr4:109984240 | A | C | 50 | a0001c0001t0033g0231 a0001c0016t0002g0051 a0001c0016t0006g0029 others(47): Show |
51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2491+699A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984240 | |||||||
chr4:109984246 | C | CA | 91 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 others(88): Show |
93 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.2491+717dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr4 | 109984246 | ||||||
chr4:109984246 | C | CAA | 42 | a0001c0001t0004g0024 a0001c0001t0004g0316 a0001c0001t0004g0320 others(39): Show |
42 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.2491+716_2491+717d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr4 | 109984246 | ||||||
chr4:109984271 | A | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+730A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984271 | |||||||
chr4:109984272 | A | G | 1 | a0001c0001t0006g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2491+731A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984272 | |||||||
chr4:109984603 | C | T | 1 | a0006c0006t0001g0163 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2491+1062C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984603 | |||||||
chr4:109984647 | A | G | 1 | a0002c0002t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2491+1106A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984647 | |||||||
chr4:109984648 | G | A | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491+1107G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984648 | |||||||
chr4:109984698 | A | G | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+1157A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984698 | |||||||
chr4:109984715 | C | G | 1 | a0001c0001t0013g0337 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2491+1174C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984715 | |||||||
chr4:109984775 | G | A | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+1234G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984775 | |||||||
chr4:109984820 | A | C | 50 | a0001c0001t0033g0231 a0001c0016t0002g0051 a0001c0016t0006g0029 others(47): Show |
51 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2491+1279A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984820 | |||||||
chr4:109984947 | C | T | 9 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2491+1406C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109984947 | |||||||
chr4:109985213 | T | C | 1 | a0001c0001t0007g0312 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2491+1672T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985213 | |||||||
chr4:109985226 | C | G | 3 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0020c0029t0031g0234 |
3 | HG02809.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2491+1685C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985226 | |||||||
chr4:109985301 | G | A | 67 | a0001c0001t0006g0249 a0001c0001t0007g0312 a0003c0003t0005g0027 others(64): Show |
69 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(66): Show |
intron_variant | MODIFIER | c.2491+1760G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985301 | |||||||
chr4:109985415 | G | A | 46 | a0001c0001t0033g0231 a0001c0016t0002g0051 a0001c0016t0006g0029 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2491+1874G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985415 | |||||||
chr4:109985453 | C | T | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2491+1912C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985453 | |||||||
chr4:109985559 | G | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491+2018G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985559 | |||||||
chr4:109985929 | T | A | 1 | a0001c0001t0012g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2492-1815T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985929 | |||||||
chr4:109985971 | A | G | 2 | a0002c0002t0006g0349 a0002c0002t0021g0341 |
2 | NA18941.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.2492-1773A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109985971 | |||||||
chr4:109986000 | T | A | 49 | a0001c0001t0033g0231 a0001c0016t0002g0051 a0001c0016t0006g0029 others(46): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.2492-1744T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986000 | |||||||
chr4:109986006 | T | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2492-1738T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986006 | |||||||
chr4:109986330 | C | T | 2 | a0002c0002t0001g0190 a0002c0002t0012g0211 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2492-1414C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986330 | |||||||
chr4:109986481 | G | A | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2492-1263G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986481 | |||||||
chr4:109986555 | C | A | 45 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2492-1189C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986555 | |||||||
chr4:109986577 | C | T | 4 | a0001c0001t0004g0330 a0001c0001t0004g0331 a0001c0001t0004g0333 others(1): Show |
4 | HG00609.hp1 HG02027.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492-1167C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986577 | |||||||
chr4:109986592 | G | A | 9 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2492-1152G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986592 | |||||||
chr4:109986748 | G | GA | 85 | a0001c0001t0006g0249 a0001c0001t0007g0312 a0001c0001t0011g0142 others(82): Show |
87 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.2492-984dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr4 | 109986748 | ||||||
chr4:109986824 | T | G | 1 | a0001c0001t0044g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2492-920T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986824 | |||||||
chr4:109986959 | T | C | 2 | a0003c0003t0005g0002 a0003c0003t0008g0002 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2492-785T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109986959 | |||||||
chr4:109987154 | C | T | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492-590C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987154 | |||||||
chr4:109987201 | G | A | 45 | a0001c0016t0002g0051 a0001c0016t0006g0029 a0003c0003t0005g0002 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2492-543G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987201 | |||||||
chr4:109987394 | C | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2492-350C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987394 | |||||||
chr4:109987433 | A | G | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2492-311A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987433 | |||||||
chr4:109987438 | C | T | 2 | a0005c0005t0006g0245 a0005c0005t0006g0248 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2492-306C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987438 | |||||||
chr4:109987523 | C | T | 1 | a0002c0002t0036g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2492-221C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987523 | |||||||
chr4:109987583 | C | T | 5 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0016c0030t0016g0305 others(2): Show |
5 | HG00738.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2492-161C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987583 | |||||||
chr4:109987638 | A | C | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2492-106A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987638 | |||||||
chr4:109987724 | G | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2492-20G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987724 | |||||||
chr4:109987725 | G | A | 12 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(9): Show |
13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2492-19G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 16/23 | chr4 | 109987725 | |||||||
chr4:109987892 | A | T | 4 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0019c0034t0020g0370 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608+32A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987892 | |||||||
chr4:109987893 | C | A | 3 | a0002c0002t0001g0213 a0002c0002t0001g0223 a0002c0002t0009g0215 |
3 | HG00423.hp2 HG02056.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2608+33C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987893 | |||||||
chr4:109987899 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2608+39T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987899 | |||||||
chr4:109987933 | C | T | 12 | a0001c0001t0014g0235 a0001c0001t0018g0233 a0005c0005t0007g0001 others(9): Show |
13 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+73C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987933 | |||||||
chr4:109987953 | A | G | 1 | a0002c0002t0001g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2608+93A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109987953 | |||||||
chr4:109988013 | A | C | 3 | a0015c0018t0017g0063 a0015c0018t0017g0134 a0022c0035t0017g0126 |
3 | HG02809.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2608+153A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988013 | |||||||
chr4:109988092 | T | C | 1 | a0001c0001t0033g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2608+232T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988092 | |||||||
chr4:109988141 | AT | A | 47 | a0001c0001t0004g0024 a0001c0001t0004g0291 a0001c0001t0004g0292 others(44): Show |
47 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.2608+284delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 109988141 | ||||||
chr4:109988192 | C | CT | 102 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(99): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2608+350dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 109988192 | ||||||
chr4:109988192 | CT | C | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2608+350delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 109988192 | ||||||
chr4:109988254 | T | C | 12 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(9): Show |
13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2609-330T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988254 | |||||||
chr4:109988546 | T | A | 3 | a0005c0005t0006g0245 a0005c0005t0006g0248 a0005c0005t0017g0244 |
3 | HG01884.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2609-38T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988546 | |||||||
chr4:109988579 | C | A | 2 | a0001c0019t0007g0140 a0001c0019t0017g0141 |
2 | HG02615.hp2 HG02630.hp1 |
splice_region_variant&intron_variant | LOW | c.2609-5C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 17/23 | chr4 | 109988579 | |||||||
chr4:109988860 | G | A | 270 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(267): Show |
277 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2734+151G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109988860 | |||||||
chr4:109988886 | A | C | 1 | a0001c0001t0004g0321 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2734+177A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109988886 | |||||||
chr4:109989184 | A | C | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2734+475A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989184 | |||||||
chr4:109989247 | G | A | 1 | a0001c0001t0002g0308 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2734+538G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989247 | |||||||
chr4:109989375 | G | A | 1 | a0004c0004t0003g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2734+666G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989375 | |||||||
chr4:109989415 | G | A | 3 | a0005c0005t0019g0012 a0005c0005t0019g0246 a0018c0023t0045g0247 |
4 | HG02559.hp1 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2734+706G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989415 | |||||||
chr4:109989594 | G | A | 1 | a0002c0002t0001g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2734+885G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989594 | |||||||
chr4:109989664 | G | A | 1 | a0019c0034t0020g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2734+955G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989664 | |||||||
chr4:109989701 | C | A | 3 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 |
3 | HG02622.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2734+992C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989701 | |||||||
chr4:109989785 | A | G | 48 | a0001c0001t0004g0024 a0001c0001t0004g0291 a0001c0001t0004g0292 others(45): Show |
48 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2734+1076A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989785 | |||||||
chr4:109989859 | G | A | 63 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(60): Show |
65 | HG00323.hp2 HG00408.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.2734+1150G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989859 | |||||||
chr4:109989869 | A | G | 272 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(269): Show |
279 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.2734+1160A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989869 | |||||||
chr4:109989924 | T | C | 271 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(268): Show |
278 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.2734+1215T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109989924 | |||||||
chr4:109990033 | T | A | 135 | a0001c0001t0004g0024 a0001c0001t0004g0291 a0001c0001t0004g0292 others(132): Show |
137 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2734+1324T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990033 | |||||||
chr4:109990153 | T | C | 374 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(371): Show |
385 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(382): Show |
intron_variant | MODIFIER | c.2734+1444T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990153 | |||||||
chr4:109990223 | C | G | 3 | a0001c0001t0040g0122 a0016c0030t0016g0305 a0019c0034t0020g0370 |
3 | HG00738.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2734+1514C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990223 | |||||||
chr4:109990271 | C | T | 13 | a0001c0001t0004g0120 a0001c0001t0007g0007 a0001c0001t0007g0118 others(10): Show |
14 | HG00738.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2734+1562C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990271 | |||||||
chr4:109990359 | T | C | 4 | a0001c0001t0002g0078 a0001c0001t0003g0077 a0001c0001t0003g0079 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.2734+1650T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990359 | |||||||
chr4:109990383 | T | C | 22 | a0001c0001t0004g0120 a0001c0001t0012g0232 a0001c0001t0014g0235 others(19): Show |
23 | HG01884.hp1 HG02486.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.2734+1674T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990383 | |||||||
chr4:109990411 | A | G | 271 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(268): Show |
278 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.2734+1702A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990411 | |||||||
chr4:109990746 | T | G | 1 | a0010c0011t0001g0179 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2734+2037T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990746 | |||||||
chr4:109990751 | T | C | 283 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(280): Show |
291 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.2734+2042T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990751 | |||||||
chr4:109990789 | G | A | 6 | a0001c0001t0007g0312 a0001c0001t0033g0231 a0005c0005t0017g0244 others(3): Show |
6 | HG02615.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2734+2080G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109990789 | |||||||
chr4:109991220 | T | TATATA | 151 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(148): Show |
155 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.2735-2025_2735-202 others(9): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109991220 | ||||||
chr4:109991370 | G | A | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-1877G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991370 | |||||||
chr4:109991401 | G | A | 1 | a0002c0002t0006g0349 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2735-1846G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991401 | |||||||
chr4:109991426 | AGTG | A | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-1817_2735-181 others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109991426 | ||||||
chr4:109991500 | G | A | 1 | a0004c0004t0003g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2735-1747G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991500 | |||||||
chr4:109991531 | G | T | 26 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(23): Show |
28 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2735-1716G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991531 | |||||||
chr4:109991544 | TAATGTAA others(10): Show |
T | 1 | a0001c0001t0027g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2735-1700_2735-168 others(21): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109991544 | ||||||
chr4:109991546 | A | T | 1 | a0006c0006t0001g0297 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2735-1701A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991546 | |||||||
chr4:109991549 | T | C | 1 | a0001c0001t0014g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2735-1698T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991549 | |||||||
chr4:109991568 | G | A | 1 | a0005c0005t0017g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2735-1679G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991568 | |||||||
chr4:109991720 | A | T | 26 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(23): Show |
28 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2735-1527A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991720 | |||||||
chr4:109991784 | T | C | 26 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(23): Show |
28 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2735-1463T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109991784 | |||||||
chr4:109992037 | A | G | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-1210A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992037 | |||||||
chr4:109992170 | T | TA | 26 | a0001c0001t0015g0373 a0002c0002t0001g0149 a0002c0002t0001g0169 others(23): Show |
27 | HG00323.hp1 HG00558.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2735-1047dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | T | TAA | 14 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0015g0175 others(11): Show |
14 | HG00423.hp2 HG00738.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.2735-1048_2735-104 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | T | TAAA | 42 | a0001c0001t0004g0291 a0001c0001t0004g0316 a0001c0001t0004g0320 others(39): Show |
42 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2735-1049_2735-104 others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | T | TAAAA | 35 | a0001c0001t0004g0322 a0001c0001t0004g0325 a0001c0001t0004g0330 others(32): Show |
36 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2735-1050_2735-104 others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | T | TAAAAA | 28 | a0001c0001t0004g0024 a0001c0001t0004g0329 a0001c0001t0004g0331 others(25): Show |
28 | HG02027.hp1 HG02027.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.2735-1051_2735-104 others(9): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | T | TAAAAAA | 24 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(21): Show |
24 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.2735-1052_2735-104 others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | T | TAAAAAAA | 12 | a0001c0001t0028g0237 a0004c0004t0003g0013 a0004c0004t0003g0266 others(9): Show |
13 | HG00735.hp2 HG02004.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.2735-1053_2735-104 others(11): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TA | T | 33 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0145 others(30): Show |
34 | HG01069.hp2 HG01070.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2735-1047delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TAA | T | 13 | a0001c0001t0007g0312 a0001c0001t0022g0236 a0001c0001t0022g0239 others(10): Show |
14 | HG02055.hp1 HG02280.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.2735-1048_2735-104 others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TAAA | T | 6 | a0001c0019t0017g0141 a0011c0012t0014g0226 a0011c0012t0014g0227 others(3): Show |
6 | HG01884.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2735-1049_2735-104 others(7): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(1): Show |
5 | HG02647.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2735-1056_2735-104 others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TAAAAAAA others(4): Show |
T | 2 | a0013c0017t0007g0136 a0013c0017t0007g0137 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2735-1057_2735-104 others(15): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TAAAAAAA others(6): Show |
T | 60 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2735-1059_2735-104 others(17): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992170 | TAAAAAAA others(7): Show |
T | 3 | a0001c0001t0002g0125 a0001c0001t0006g0107 a0001c0007t0002g0102 |
3 | HG02895.hp2 HG03491.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2735-1060_2735-104 others(18): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992170 | ||||||
chr4:109992191 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0040g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2735-1054_2735-104 others(16): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109992191 | ||||||
chr4:109992205 | G | A | 1 | a0005c0005t0038g0274 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2735-1042G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992205 | |||||||
chr4:109992207 | G | C | 1 | a0005c0005t0046g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2735-1040G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992207 | |||||||
chr4:109992242 | C | T | 1 | a0020c0029t0031g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2735-1005C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992242 | |||||||
chr4:109992257 | G | A | 1 | a0002c0002t0001g0192 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2735-990G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992257 | |||||||
chr4:109992331 | G | A | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2735-916G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992331 | |||||||
chr4:109992691 | C | T | 6 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(3): Show |
7 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2735-556C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992691 | |||||||
chr4:109992827 | C | G | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-420C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992827 | |||||||
chr4:109992847 | A | C | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-400A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992847 | |||||||
chr4:109992954 | G | A | 8 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2735-293G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992954 | |||||||
chr4:109992954 | G | C | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-293G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992954 | |||||||
chr4:109992963 | G | A | 374 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(371): Show |
385 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(382): Show |
intron_variant | MODIFIER | c.2735-284G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992963 | |||||||
chr4:109992986 | C | T | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-261C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992986 | |||||||
chr4:109992992 | A | AT | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-255_2735-254i others(3): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992992 | |||||||
chr4:109992993 | A | G | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-254A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992993 | |||||||
chr4:109992994 | A | T | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-253A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109992994 | |||||||
chr4:109993034 | CATGTATA others(3): Show |
C | 10 | a0001c0001t0004g0323 a0001c0001t0004g0327 a0001c0001t0004g0328 others(7): Show |
10 | HG00438.hp2 NA18942.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.2735-207_2735-198d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109993034 | ||||||
chr4:109993062 | C | G | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2735-185C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109993062 | |||||||
chr4:109993067 | G | A | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2735-180G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109993067 | |||||||
chr4:109993110 | TA | T | 8 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2735-130delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr4 | 109993110 | ||||||
chr4:109993125 | G | C | 11 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2735-122G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 18/23 | chr4 | 109993125 | |||||||
chr4:109993564 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2857+195G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993564 | |||||||
chr4:109993595 | A | G | 25 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(22): Show |
27 | HG00735.hp2 HG01884.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.2857+226A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993595 | |||||||
chr4:109993684 | TGCAGGGC others(3): Show |
T | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2857+321_2857+330d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109993684 | ||||||
chr4:109993864 | A | G | 6 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0018 others(3): Show |
6 | HG02818.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2857+495A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993864 | |||||||
chr4:109993954 | A | G | 1 | a0001c0001t0014g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2857+585A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109993954 | |||||||
chr4:109994031 | G | GT | 69 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(66): Show |
71 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2857+675dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109994031 | ||||||
chr4:109994031 | G | GTT | 103 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(100): Show |
104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2857+674_2857+675d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109994031 | ||||||
chr4:109994031 | GT | G | 10 | a0001c0001t0002g0069 a0001c0001t0011g0142 a0001c0001t0011g0143 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2857+675delT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 109994031 | ||||||
chr4:109994352 | C | A | 1 | a0003c0003t0008g0046 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2858-381C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994352 | |||||||
chr4:109994402 | A | C | 2 | a0002c0002t0006g0349 a0002c0002t0021g0341 |
2 | NA18941.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.2858-331A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994402 | |||||||
chr4:109994460 | A | T | 1 | a0016c0030t0016g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2858-273A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994460 | |||||||
chr4:109994549 | G | A | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2858-184G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994549 | |||||||
chr4:109994592 | A | T | 1 | a0004c0004t0010g0062 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2858-141A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 19/23 | chr4 | 109994592 | |||||||
chr4:109995024 | G | A | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3005+144G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995024 | |||||||
chr4:109995079 | C | T | 1 | a0002c0002t0001g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3005+199C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995079 | |||||||
chr4:109995193 | G | A | 11 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3005+313G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995193 | |||||||
chr4:109995480 | G | A | 12 | a0002c0002t0001g0169 a0002c0002t0001g0171 a0002c0002t0006g0080 others(9): Show |
12 | HG00673.hp2 HG02129.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.3005+600G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995480 | |||||||
chr4:109995680 | G | A | 1 | a0001c0001t0027g0068 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3005+800G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995680 | |||||||
chr4:109995866 | G | C | 1 | a0001c0001t0004g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3005+986G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995866 | |||||||
chr4:109995961 | T | G | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3005+1081T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109995961 | |||||||
chr4:109996071 | G | A | 3 | a0003c0003t0005g0054 a0003c0003t0008g0056 a0003c0003t0008g0059 |
3 | HG02027.hp1 NA18947.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.3005+1191G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996071 | |||||||
chr4:109996080 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3005+1200C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996080 | |||||||
chr4:109996331 | T | C | 48 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(45): Show |
49 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.3005+1451T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996331 | |||||||
chr4:109996369 | G | T | 20 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(17): Show |
22 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3005+1489G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996369 | |||||||
chr4:109996470 | A | C | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3005+1590A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996470 | |||||||
chr4:109996918 | C | A | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3005+2038C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109996918 | |||||||
chr4:109997001 | A | AT | 8 | a0002c0002t0001g0165 a0002c0002t0001g0181 a0002c0002t0001g0182 others(5): Show |
9 | HG01074.hp2 HG01081.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.3005+2132dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 109997001 | ||||||
chr4:109997158 | C | T | 1 | a0002c0002t0002g0110 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3005+2278C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997158 | |||||||
chr4:109997231 | G | T | 5 | a0009c0010t0016g0344 a0009c0010t0016g0345 a0009c0010t0016g0346 others(2): Show |
5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3005+2351G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997231 | |||||||
chr4:109997302 | G | C | 1 | a0001c0001t0011g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3006-2377G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997302 | |||||||
chr4:109997488 | G | A | 1 | a0001c0001t0006g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3006-2191G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997488 | |||||||
chr4:109997531 | A | G | 268 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(265): Show |
275 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.3006-2148A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997531 | |||||||
chr4:109997663 | G | A | 1 | a0004c0032t0003g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3006-2016G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997663 | |||||||
chr4:109997777 | C | G | 1 | a0002c0002t0001g0218 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3006-1902C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997777 | |||||||
chr4:109997818 | G | A | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006-1861G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997818 | |||||||
chr4:109997820 | A | G | 50 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3006-1859A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997820 | |||||||
chr4:109997935 | C | T | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3006-1744C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109997935 | |||||||
chr4:109998038 | T | A | 1 | a0001c0001t0018g0233 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3006-1641T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998038 | |||||||
chr4:109998203 | T | C | 5 | a0009c0010t0016g0344 a0009c0010t0016g0345 a0009c0010t0016g0346 others(2): Show |
5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006-1476T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998203 | |||||||
chr4:109998244 | C | T | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3006-1435C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998244 | |||||||
chr4:109998312 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3006-1367C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998312 | |||||||
chr4:109998738 | G | A | 1 | a0005c0005t0017g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3006-941G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998738 | |||||||
chr4:109998740 | G | C | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006-939G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998740 | |||||||
chr4:109998903 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3006-776A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998903 | |||||||
chr4:109998943 | A | G | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3006-736A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109998943 | |||||||
chr4:109999015 | GAC | G | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3006-662_3006-661d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 109999015 | ||||||
chr4:109999075 | T | C | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3006-604T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999075 | |||||||
chr4:109999095 | G | A | 1 | a0001c0001t0018g0233 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3006-584G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999095 | |||||||
chr4:109999143 | A | G | 50 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3006-536A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999143 | |||||||
chr4:109999175 | A | C | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006-504A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999175 | |||||||
chr4:109999217 | G | A | 1 | a0003c0003t0005g0041 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3006-462G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999217 | |||||||
chr4:109999291 | A | G | 3 | a0008c0009t0001g0184 a0008c0009t0001g0185 a0008c0009t0009g0183 |
3 | NA18946.hp1 NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3006-388A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999291 | |||||||
chr4:109999297 | T | G | 1 | a0001c0001t0014g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3006-382T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999297 | |||||||
chr4:109999314 | T | C | 1 | a0002c0002t0001g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3006-365T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999314 | |||||||
chr4:109999568 | G | A | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3006-111G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999568 | |||||||
chr4:109999665 | G | A | 1 | a0012c0014t0007g0138 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3006-14G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 20/23 | chr4 | 109999665 | |||||||
chr4:109999972 | C | G | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3173+126C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 109999972 | |||||||
chr4:110000049 | C | T | 1 | a0001c0001t0011g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3173+203C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000049 | |||||||
chr4:110000112 | G | A | 1 | a0022c0035t0017g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3173+266G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000112 | |||||||
chr4:110000131 | A | G | 1 | a0001c0001t0013g0324 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3173+285A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000131 | |||||||
chr4:110000218 | T | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(61): Show |
66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3173+372T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000218 | |||||||
chr4:110000250 | C | CA | 34 | a0001c0001t0014g0229 a0001c0001t0014g0235 a0001c0001t0018g0233 others(31): Show |
36 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.3173+424dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | ||||||
chr4:110000250 | CA | C | 18 | a0001c0001t0002g0307 a0001c0001t0004g0120 a0001c0001t0006g0099 others(15): Show |
18 | HG00738.hp1 HG01975.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.3173+424delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | ||||||
chr4:110000250 | CAA | C | 98 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(95): Show |
101 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3173+423_3173+424d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | ||||||
chr4:110000250 | CAAA | C | 9 | a0001c0001t0002g0090 a0003c0003t0008g0034 a0003c0003t0008g0036 others(6): Show |
9 | HG00423.hp1 HG00621.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3173+422_3173+424d others(5): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110000250 | ||||||
chr4:110000259 | A | G | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3173+413A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000259 | |||||||
chr4:110000420 | G | A | 2 | a0001c0001t0022g0236 a0001c0001t0022g0239 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3173+574G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000420 | |||||||
chr4:110000832 | A | G | 1 | a0002c0002t0001g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3173+986A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110000832 | |||||||
chr4:110001038 | T | C | 56 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.3173+1192T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001038 | |||||||
chr4:110001340 | T | C | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3173+1494T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001340 | |||||||
chr4:110001423 | A | G | 64 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(61): Show |
66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3173+1577A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001423 | |||||||
chr4:110001524 | G | A | 115 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(112): Show |
116 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.3173+1678G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001524 | |||||||
chr4:110001530 | GA | G | 50 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(47): Show |
51 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.3173+1693delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110001530 | ||||||
chr4:110001565 | C | T | 1 | a0004c0004t0010g0272 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3173+1719C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001565 | |||||||
chr4:110001722 | A | G | 1 | a0001c0001t0006g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3173+1876A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001722 | |||||||
chr4:110001740 | A | G | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3173+1894A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110001740 | |||||||
chr4:110002040 | G | A | 1 | a0003c0003t0008g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3173+2194G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002040 | |||||||
chr4:110002047 | C | T | 3 | a0002c0002t0023g0220 a0002c0002t0023g0222 a0002c0002t0036g0221 |
3 | HG02280.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3173+2201C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002047 | |||||||
chr4:110002088 | A | G | 1 | a0002c0002t0021g0314 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3173+2242A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002088 | |||||||
chr4:110002172 | G | A | 110 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(107): Show |
111 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.3173+2326G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002172 | |||||||
chr4:110002287 | G | A | 1 | a0002c0002t0036g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3174-2218G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002287 | |||||||
chr4:110002380 | C | T | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3174-2125C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002380 | |||||||
chr4:110002436 | T | C | 64 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(61): Show |
66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.3174-2069T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002436 | |||||||
chr4:110002537 | T | G | 50 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3174-1968T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002537 | |||||||
chr4:110002542 | T | G | 13 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0028g0237 others(10): Show |
13 | HG00735.hp2 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.3174-1963T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002542 | |||||||
chr4:110002559 | C | A | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3174-1946C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002559 | |||||||
chr4:110002635 | G | C | 109 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(106): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.3174-1870G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002635 | |||||||
chr4:110002667 | A | T | 1 | a0002c0002t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3174-1838A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002667 | |||||||
chr4:110002774 | A | G | 1 | a0005c0005t0007g0275 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3174-1731A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002774 | |||||||
chr4:110002783 | C | T | 142 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(139): Show |
145 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.3174-1722C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002783 | |||||||
chr4:110002875 | C | T | 5 | a0009c0010t0016g0344 a0009c0010t0016g0345 a0009c0010t0016g0346 others(2): Show |
5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3174-1630C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110002875 | |||||||
chr4:110003056 | G | A | 78 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(75): Show |
81 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.3174-1449G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003056 | |||||||
chr4:110003069 | G | A | 11 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3174-1436G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003069 | |||||||
chr4:110003178 | C | G | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3174-1327C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003178 | |||||||
chr4:110003204 | G | T | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3174-1301G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003204 | |||||||
chr4:110003401 | T | C | 1 | a0002c0002t0006g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3174-1104T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003401 | |||||||
chr4:110003486 | G | C | 198 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(195): Show |
203 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.3174-1019G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003486 | |||||||
chr4:110003553 | G | C | 27 | a0001c0001t0014g0229 a0001c0001t0014g0235 a0001c0001t0018g0233 others(24): Show |
29 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3174-952G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003553 | |||||||
chr4:110003585 | A | T | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3174-920A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003585 | |||||||
chr4:110003616 | C | T | 203 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(200): Show |
208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3174-889C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003616 | |||||||
chr4:110003672 | G | A | 1 | a0004c0004t0003g0242 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3174-833G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003672 | |||||||
chr4:110003719 | A | T | 8 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3174-786A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003719 | |||||||
chr4:110003999 | A | G | 1 | a0004c0004t0003g0252 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3174-506A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110003999 | |||||||
chr4:110004092 | T | C | 8 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3174-413T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004092 | |||||||
chr4:110004191 | C | A | 2 | a0001c0001t0004g0316 a0001c0001t0013g0337 |
2 | NA18968.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3174-314C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004191 | |||||||
chr4:110004198 | A | G | 1 | a0002c0002t0001g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3174-307A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004198 | |||||||
chr4:110004208 | G | GCATA | 8 | a0001c0001t0004g0120 a0001c0001t0004g0291 a0001c0001t0004g0292 others(5): Show |
8 | HG00558.hp1 HG00609.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.3174-290_3174-287d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004208 | ||||||
chr4:110004208 | GCATA | G | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3174-290_3174-287d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004208 | ||||||
chr4:110004211 | T | TACAC | 18 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(15): Show |
19 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.3174-291_3174-290i others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | ||||||
chr4:110004211 | T | TACACAC | 12 | a0004c0004t0003g0258 a0004c0004t0003g0259 a0004c0004t0003g0281 others(9): Show |
12 | NA18939.hp2 NA18947.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.3174-291_3174-290i others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | ||||||
chr4:110004211 | TACATACA others(3): Show |
T | 27 | a0001c0001t0007g0312 a0001c0001t0014g0229 a0001c0001t0018g0233 others(24): Show |
29 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3174-290_3174-281d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | ||||||
chr4:110004211 | TACATACA others(5): Show |
T | 2 | a0018c0023t0045g0247 a0020c0029t0031g0234 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3174-290_3174-279d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004211 | ||||||
chr4:110004213 | CAT | C | 8 | a0001c0001t0011g0146 a0001c0001t0011g0147 a0001c0001t0011g0148 others(5): Show |
8 | HG01109.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3174-290_3174-289d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004213 | ||||||
chr4:110004215 | T | C | 53 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(50): Show |
55 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.3174-290T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004215 | |||||||
chr4:110004215 | T | TAC | 55 | a0001c0001t0002g0069 a0001c0001t0002g0093 a0001c0001t0025g0097 others(52): Show |
56 | HG00609.hp2 HG00673.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3174-254_3174-253d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | T | TACAC | 15 | a0001c0001t0006g0249 a0001c0007t0002g0117 a0002c0002t0001g0014 others(12): Show |
16 | HG00323.hp1 HG02015.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.3174-256_3174-253d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | T | TACACAC | 6 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(3): Show |
6 | HG02074.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3174-258_3174-253d others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | T | TACACACA others(13): Show |
1 | a0002c0002t0006g0349 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3174-272_3174-253d others(22): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | T | TACACACA others(19): Show |
2 | a0002c0002t0001g0008 a0002c0002t0021g0341 |
2 | NA18941.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.3174-278_3174-253d others(28): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | T | TACATAC | 21 | a0001c0001t0004g0330 a0001c0001t0004g0331 a0001c0001t0004g0332 others(18): Show |
21 | HG00733.hp2 HG01070.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.3174-287_3174-286i others(8): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | T | TACATACA others(1): Show |
27 | a0001c0001t0004g0024 a0001c0001t0004g0316 a0001c0001t0004g0320 others(24): Show |
27 | HG00408.hp1 HG00438.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.3174-287_3174-286i others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | TACAC | T | 6 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0002c0002t0001g0015 others(3): Show |
6 | HG01070.hp2 HG02155.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3174-256_3174-253d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004215 | TACACACA others(1): Show |
T | 3 | a0001c0001t0002g0308 a0001c0001t0002g0310 a0001c0001t0006g0309 |
3 | NA18967.hp2 NA18969.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3174-260_3174-253d others(10): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 110004215 | ||||||
chr4:110004253 | A | C | 1 | a0001c0027t0004g0326 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3174-252A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004253 | |||||||
chr4:110004303 | G | A | 107 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(104): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.3174-202G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004303 | |||||||
chr4:110004313 | C | T | 107 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(104): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.3174-192C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004313 | |||||||
chr4:110004336 | C | A | 200 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(197): Show |
205 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.3174-169C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004336 | |||||||
chr4:110004375 | A | G | 1 | a0002c0002t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3174-130A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 21/23 | chr4 | 110004375 | |||||||
chr4:110004672 | C | T | 1 | a0002c0002t0006g0351 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3291+50C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110004672 | |||||||
chr4:110004750 | C | A | 1 | a0001c0001t0013g0358 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3291+128C>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110004750 | |||||||
chr4:110004768 | G | A | 1 | a0001c0001t0012g0372 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3291+146G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110004768 | |||||||
chr4:110005036 | C | CT | 114 | a0001c0001t0002g0065 a0001c0001t0002g0085 a0001c0001t0002g0093 others(111): Show |
117 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.3291+438dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | ||||||
chr4:110005036 | C | CTT | 28 | a0001c0001t0002g0124 a0001c0001t0003g0088 a0001c0007t0002g0100 others(25): Show |
28 | HG00423.hp1 HG00621.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.3291+437_3291+438d others(4): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | ||||||
chr4:110005036 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3291+429_3291+438d others(12): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | ||||||
chr4:110005036 | CTTTTTTT others(4): Show |
C | 15 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(12): Show |
16 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.3291+428_3291+438d others(13): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | ||||||
chr4:110005036 | CTTTTTTT others(5): Show |
C | 1 | a0021c0025t0021g0279 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3291+427_3291+438d others(14): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | ||||||
chr4:110005036 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3291+426_3291+438d others(15): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110005036 | ||||||
chr4:110005353 | T | C | 4 | a0002c0002t0001g0174 a0002c0002t0001g0176 a0002c0002t0002g0110 others(1): Show |
4 | HG02165.hp2 NA18954.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3291+731T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005353 | |||||||
chr4:110005371 | A | G | 140 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(137): Show |
145 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.3291+749A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005371 | |||||||
chr4:110005377 | C | T | 49 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0292 others(46): Show |
49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.3291+755C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005377 | |||||||
chr4:110005525 | T | C | 1 | a0003c0003t0005g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3291+903T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005525 | |||||||
chr4:110005574 | G | A | 201 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(198): Show |
206 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.3291+952G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110005574 | |||||||
chr4:110006047 | GA | G | 89 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(86): Show |
93 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.3291+1432delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110006047 | ||||||
chr4:110006071 | T | G | 1 | a0002c0002t0035g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3291+1449T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006071 | |||||||
chr4:110006183 | TA | T | 201 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(198): Show |
206 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.3291+1572delA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110006183 | ||||||
chr4:110006236 | TCAAGAGA others(25): Show |
T | 9 | a0001c0001t0002g0065 a0001c0007t0002g0006 a0001c0007t0002g0100 others(6): Show |
10 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3291+1621_3291+165 others(36): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr4 | 110006236 | ||||||
chr4:110006373 | G | A | 3 | a0001c0001t0002g0070 a0001c0001t0012g0212 a0001c0001t0012g0214 |
3 | HG00408.hp2 NA18951.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3291+1751G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006373 | |||||||
chr4:110006377 | T | C | 8 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3291+1755T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006377 | |||||||
chr4:110006407 | G | C | 288 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(285): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.3292-1745G>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006407 | |||||||
chr4:110006477 | T | A | 2 | a0018c0023t0045g0247 a0020c0029t0031g0234 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3292-1675T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006477 | |||||||
chr4:110006648 | G | A | 1 | a0005c0005t0017g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3292-1504G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006648 | |||||||
chr4:110006709 | A | T | 203 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(200): Show |
208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3292-1443A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006709 | |||||||
chr4:110006772 | G | A | 203 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(200): Show |
208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3292-1380G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006772 | |||||||
chr4:110006851 | G | A | 6 | a0001c0001t0022g0236 a0001c0001t0022g0239 a0001c0001t0029g0238 others(3): Show |
7 | HG02055.hp1 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3292-1301G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110006851 | |||||||
chr4:110007060 | C | T | 3 | a0012c0014t0007g0135 a0012c0014t0007g0138 a0012c0014t0007g0139 |
3 | HG02622.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3292-1092C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007060 | |||||||
chr4:110007300 | T | A | 1 | a0004c0004t0003g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3292-852T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007300 | |||||||
chr4:110007482 | A | G | 2 | a0003c0003t0005g0002 a0003c0003t0008g0002 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3292-670A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007482 | |||||||
chr4:110007646 | A | G | 1 | a0002c0002t0009g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3292-506A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007646 | |||||||
chr4:110007659 | A | T | 27 | a0001c0001t0007g0312 a0001c0001t0014g0229 a0001c0001t0014g0235 others(24): Show |
29 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.3292-493A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007659 | |||||||
chr4:110007730 | A | G | 2 | a0001c0001t0028g0237 a0001c0001t0033g0231 |
2 | HG00735.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3292-422A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007730 | |||||||
chr4:110007735 | G | A | 1 | a0001c0001t0040g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3292-417G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007735 | |||||||
chr4:110007756 | G | A | 2 | a0018c0023t0045g0247 a0020c0029t0031g0234 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3292-396G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007756 | |||||||
chr4:110007793 | T | G | 203 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(200): Show |
208 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.3292-359T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007793 | |||||||
chr4:110007807 | C | G | 5 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3292-345C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007807 | |||||||
chr4:110007820 | A | C | 1 | a0005c0005t0007g0278 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3292-332A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007820 | |||||||
chr4:110007972 | G | A | 74 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(71): Show |
77 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.3292-180G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 22/23 | chr4 | 110007972 | |||||||
chr4:110008353 | C | G | 5 | a0001c0001t0020g0011 a0001c0001t0020g0230 a0001c0001t0034g0011 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3370+123C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008353 | |||||||
chr4:110008382 | G | A | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+152G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008382 | |||||||
chr4:110008476 | T | C | 1 | a0002c0002t0009g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3370+246T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008476 | |||||||
chr4:110008497 | G | A | 47 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(44): Show |
48 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.3370+267G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008497 | |||||||
chr4:110008573 | C | T | 44 | a0001c0001t0004g0024 a0001c0001t0004g0316 a0001c0001t0004g0320 others(41): Show |
44 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.3370+343C>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008573 | |||||||
chr4:110008601 | A | G | 5 | a0009c0010t0016g0344 a0009c0010t0016g0345 a0009c0010t0016g0346 others(2): Show |
5 | HG01975.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+371A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008601 | |||||||
chr4:110008657 | C | G | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+427C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008657 | |||||||
chr4:110008928 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3370+698G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008928 | |||||||
chr4:110008938 | A | G | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3370+708A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008938 | |||||||
chr4:110008970 | G | A | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3370+740G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110008970 | |||||||
chr4:110009057 | A | G | 50 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3370+827A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009057 | |||||||
chr4:110009186 | C | G | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+956C>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009186 | |||||||
chr4:110009235 | T | A | 50 | a0001c0001t0004g0024 a0001c0001t0004g0120 a0001c0001t0004g0291 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3370+1005T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009235 | |||||||
chr4:110009520 | A | G | 5 | a0001c0019t0017g0141 a0005c0005t0017g0244 a0015c0018t0017g0063 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3370+1290A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009520 | |||||||
chr4:110009638 | A | G | 202 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(199): Show |
207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3370+1408A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009638 | |||||||
chr4:110009834 | A | G | 1 | a0002c0002t0001g0306 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3371-1368A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009834 | |||||||
chr4:110009949 | T | C | 202 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(199): Show |
207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3371-1253T>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110009949 | |||||||
chr4:110010064 | G | A | 7 | a0001c0001t0007g0007 a0001c0001t0007g0118 a0001c0001t0007g0119 others(4): Show |
8 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3371-1138G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010064 | |||||||
chr4:110010074 | A | G | 1 | a0001c0001t0002g0310 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3371-1128A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010074 | |||||||
chr4:110010084 | G | A | 1 | a0001c0001t0015g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3371-1118G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010084 | |||||||
chr4:110010246 | A | C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0109 |
2 | NA18959.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.3371-956A>C | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010246 | |||||||
chr4:110010279 | A | T | 3 | a0011c0012t0014g0226 a0011c0012t0014g0227 a0011c0012t0014g0228 |
3 | HG01884.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3371-923A>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010279 | |||||||
chr4:110010295 | CTCTA | C | 3 | a0006c0006t0001g0009 a0006c0006t0001g0161 a0006c0006t0001g0217 |
4 | HG03017.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3371-902_3371-899d others(6): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr4 | 110010295 | ||||||
chr4:110010403 | T | G | 1 | a0001c0001t0002g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3371-799T>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010403 | |||||||
chr4:110010407 | A | AT | 25 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(22): Show |
26 | HG01109.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3371-788dupT | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr4 | 110010407 | ||||||
chr4:110010413 | T | TA | 3 | a0001c0001t0004g0347 a0003c0003t0026g0020 a0005c0005t0038g0274 |
3 | NA18975.hp1 NA19002.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3371-789_3371-788i others(3): Show |
EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010413 | |||||||
chr4:110010414 | T | A | 3 | a0001c0001t0004g0347 a0003c0003t0026g0020 a0005c0005t0038g0274 |
3 | NA18975.hp1 NA19002.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3371-788T>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010414 | |||||||
chr4:110010414 | T | TA | 172 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(169): Show |
176 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.3371-781dupA | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr4 | 110010414 | ||||||
chr4:110010630 | A | G | 202 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0001t0003g0088 others(199): Show |
207 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3371-572A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010630 | |||||||
chr4:110010662 | G | A | 1 | a0001c0001t0040g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3371-540G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010662 | |||||||
chr4:110010783 | G | T | 46 | a0003c0003t0005g0002 a0003c0003t0005g0003 a0003c0003t0005g0019 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3371-419G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010783 | |||||||
chr4:110010790 | G | T | 2 | a0018c0023t0045g0247 a0020c0029t0031g0234 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3371-412G>T | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010790 | |||||||
chr4:110010985 | G | A | 3 | a0006c0006t0001g0009 a0006c0006t0001g0161 a0006c0006t0001g0217 |
4 | HG03017.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3371-217G>A | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110010985 | |||||||
chr4:110011048 | A | G | 1 | a0005c0005t0019g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3371-154A>G | EGF | ENSG00000138798.13 | transcript | ENST00000265171.10 | protein_coding | 23/23 | chr4 | 110011048 |