Item | Value |
---|---|
geneid | 57724 |
ensemblid | ENSG00000152223.16 |
hgncid | 29331 |
symbol | EPG5 |
name | ectopic P-granules 5 autophagy tethering factor |
refseq_nuc | NM_020964.3 |
refseq_prot | NP_066015.2 |
ensembl_nuc | ENST00000282041.11 |
ensembl_prot | ENSP00000282041.4 |
mane_status | MANE Select |
chr | chr18 |
start | 45847609 |
end | 45967329 |
strand | - |
ver | v1.2 |
region | chr18:45847609-45967329 |
region5000 | chr18:45842609-45972329 |
regionname0 | EPG5_chr18_45847609_45967329 |
regionname5000 | EPG5_chr18_45842609_45972329 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2579 | 106 | 14 | 22 | 49 | 5 | 15 | 39 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0002 | 0/0 | 2579 | 76 | 14 | 15 | 35 | 3 | 9 | 29 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0003 | 0/0 | 2579 | 26 | 4 | 1 | 16 | 0 | 5 | 16 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0004 | 1/0 | 2579 | 16 | 2 | 7 | 1 | 0 | 5 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0005 | 0/0 | 2579 | 16 | 12 | 1 | 1 | 1 | 1 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0006 | 0/0 | 2579 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0007 | 0/0 | 2579 | 7 | 1 | 1 | 1 | 1 | 3 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0008 | 0/0 | 2579 | 6 | 0 | 2 | 3 | 0 | 1 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0009 | 0/0 | 2579 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0010 | 0/0 | 2579 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0011 | 0/0 | 2579 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0012 | 0/0 | 2579 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0013 | 0/0 | 2579 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0014 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0015 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0016 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0017 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0018 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0019 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0020 | 0/0 | 2579 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0021 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0022 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0023 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0024 | 0/0 | 87 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(82): Show |
chr18 | 45842609 | 45972329 |
a0025 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0026 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0027 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0028 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0029 | 0/0 | 2579 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0030 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
a0031 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | MAEAV others(2574): Show |
chr18 | 45842609 | 45972329 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 7737 | 100 | 14 | 20 | 45 | 5 | 15 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0001c0021 | 0/0 | 7737 | 2 | 0 | 2 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0001c0024 | 0/0 | 7737 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0001c0030 | 0/0 | 7737 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0001c0034 | 0/0 | 7737 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0002c0002 | 0/0 | 7737 | 68 | 13 | 14 | 30 | 2 | 9 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0002c0009 | 0/0 | 7737 | 5 | 0 | 0 | 5 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0002c0033 | 0/0 | 7737 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0002c0038 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0002c0040 | 0/0 | 7737 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0003c0003 | 0/0 | 7737 | 22 | 1 | 1 | 16 | 0 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0003c0013 | 0/0 | 7737 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0003c0044 | 0/0 | 7737 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0004c0005 | 1/0 | 7737 | 11 | 1 | 5 | 1 | 0 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0004c0014 | 0/0 | 7737 | 3 | 1 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0004c0025 | 0/0 | 7737 | 2 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0005c0004 | 0/0 | 7737 | 14 | 10 | 1 | 1 | 1 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0005c0027 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0005c0048 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0006c0011 | 0/0 | 7737 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0006c0012 | 0/0 | 7737 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0006c0037 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0007c0006 | 0/0 | 7737 | 7 | 1 | 1 | 1 | 1 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0008c0008 | 0/0 | 7737 | 6 | 0 | 2 | 3 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0009c0007 | 0/0 | 7737 | 6 | 6 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0010c0010 | 0/0 | 7737 | 4 | 0 | 0 | 4 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0011c0022 | 0/0 | 7737 | 2 | 1 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0011c0039 | 0/0 | 7737 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0012c0020 | 0/0 | 7737 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0013c0026 | 0/0 | 7737 | 2 | 0 | 0 | 0 | 2 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0014c0015 | 0/0 | 7737 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0015c0042 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0015c0043 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0016c0018 | 0/0 | 7737 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0017c0019 | 0/0 | 7737 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0018c0017 | 0/0 | 7737 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0019c0016 | 0/0 | 7737 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0020c0023 | 0/0 | 7737 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0021c0032 | 0/0 | 7737 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0022c0031 | 0/0 | 7737 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0023c0049 | 0/0 | 7737 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0024c0029 | 0/0 | 7737 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0025c0045 | 0/0 | 7737 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0026c0041 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0027c0036 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0028c0028 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0029c0046 | 0/0 | 7737 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0030c0035 | 0/0 | 7737 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 | ||
a0031c0047 | 0/0 | 7737 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGGC others(7732): Show |
chr18 | 45842609 | 45972329 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 12688 | 63 | 7 | 10 | 33 | 4 | 8 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0002 | 0/0 | 12687 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0003 | 0/0 | 12688 | 5 | 1 | 2 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0004 | 0/0 | 12687 | 16 | 4 | 5 | 2 | 1 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0005 | 0/0 | 12694 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0009 | 0/0 | 12689 | 4 | 0 | 1 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0011 | 0/0 | 12690 | 3 | 0 | 2 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12685): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0012 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0032 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0036 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0039 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0040 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0001c0001t0043 | 0/0 | 12687 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0001c0021t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0021t0004 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0001c0024t0001 | 0/0 | 12688 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0030t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0001c0034t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0001 | 0/0 | 12688 | 4 | 2 | 1 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0002 | 0/0 | 12687 | 41 | 1 | 11 | 23 | 1 | 5 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0003 | 0/0 | 12688 | 2 | 0 | 0 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0004 | 0/0 | 12687 | 4 | 2 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0008 | 0/0 | 12688 | 6 | 1 | 0 | 3 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0014 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0017 | 0/0 | 12694 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0024 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0025 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0026 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0027 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0029 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0030 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0031 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0037 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0002t0038 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0009t0002 | 0/0 | 12687 | 5 | 0 | 0 | 5 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0002c0033t0001 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0002c0038t0007 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0002c0040t0002 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0001 | 0/0 | 12688 | 4 | 1 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0002 | 0/0 | 12687 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0003 | 0/0 | 12688 | 12 | 0 | 1 | 9 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0012 | 0/0 | 12689 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0015 | 0/0 | 12687 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0016 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0003c0003t0042 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0003c0013t0001 | 0/0 | 12688 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0003c0044t0003 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0004c0005t0003 | 1/0 | 12688 | 6 | 0 | 3 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0004c0005t0005 | 0/0 | 12694 | 2 | 0 | 1 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0004c0005t0016 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0004c0005t0033 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0004c0005t0034 | 0/0 | 12690 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12685): Show |
chr18 | 45842609 | 45972329 |
a0004c0014t0003 | 0/0 | 12688 | 2 | 1 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0004c0014t0035 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0004c0025t0003 | 0/0 | 12688 | 2 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0003 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0004 | 0/0 | 12687 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0005 | 0/0 | 12694 | 8 | 8 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0009 | 0/0 | 12689 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0015 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0005c0004t0044 | 0/0 | 12689 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0005c0027t0005 | 0/0 | 12694 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0005c0048t0003 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0006c0011t0006 | 0/0 | 12692 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12687): Show |
chr18 | 45842609 | 45972329 |
a0006c0011t0013 | 0/0 | 12693 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12688): Show |
chr18 | 45842609 | 45972329 |
a0006c0012t0006 | 0/0 | 12692 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12687): Show |
chr18 | 45842609 | 45972329 |
a0006c0037t0006 | 0/0 | 12692 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12687): Show |
chr18 | 45842609 | 45972329 |
a0007c0006t0003 | 0/0 | 12688 | 7 | 1 | 1 | 1 | 1 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0008c0008t0001 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0008c0008t0002 | 0/0 | 12687 | 4 | 0 | 1 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0008c0008t0028 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0009c0007t0007 | 0/0 | 12691 | 6 | 6 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0010c0010t0001 | 0/0 | 12688 | 4 | 0 | 0 | 4 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0011c0022t0020 | 0/0 | 12689 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0011c0022t0021 | 0/0 | 12689 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12684): Show |
chr18 | 45842609 | 45972329 |
a0011c0039t0002 | 0/0 | 12687 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0012c0020t0004 | 0/0 | 12687 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0013c0026t0005 | 0/0 | 12694 | 2 | 0 | 0 | 0 | 2 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0014c0015t0014 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0014c0015t0019 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0015c0042t0022 | 0/0 | 12690 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12685): Show |
chr18 | 45842609 | 45972329 |
a0015c0043t0023 | 0/0 | 12692 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12687): Show |
chr18 | 45842609 | 45972329 |
a0016c0018t0001 | 0/0 | 12688 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0017c0019t0006 | 0/0 | 12692 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12687): Show |
chr18 | 45842609 | 45972329 |
a0018c0017t0010 | 0/0 | 12694 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0019c0016t0010 | 0/0 | 12694 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12689): Show |
chr18 | 45842609 | 45972329 |
a0020c0023t0002 | 0/0 | 12687 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
a0021c0032t0041 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0022c0031t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0023c0049t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0024c0029t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0025c0045t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0026c0041t0007 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0027c0036t0013 | 0/0 | 12693 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12688): Show |
chr18 | 45842609 | 45972329 |
a0028c0028t0018 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12686): Show |
chr18 | 45842609 | 45972329 |
a0029c0046t0003 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0030c0035t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12683): Show |
chr18 | 45842609 | 45972329 |
a0031c0047t0002 | 0/0 | 12687 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | ATGTG others(12682): Show |
chr18 | 45842609 | 45972329 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0010 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0011g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0032g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0036g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0039g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0040g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0001t0043g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0021t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0021t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0024t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0024t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0030t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0001c0034t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0008g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0017g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0024g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0025g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0029g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0030g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0031g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0037g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0002t0038g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0009t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0009t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0009t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0009t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0009t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0033t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0038t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0002c0040t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0016g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0003t0042g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0013t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0013t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0003c0044t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0003g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0016g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0033g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0005t0034g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0014t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0014t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0014t0035g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0025t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0004c0025t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0004t0044g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0027t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0005c0048t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0011t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0011t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0011t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0011t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0012t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0012t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0012t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0012t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0006c0037t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0007c0006t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0008c0008t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0008c0008t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0008c0008t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0008c0008t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0008c0008t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0008c0008t0028g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0009c0007t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0009c0007t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0009c0007t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0009c0007t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0009c0007t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0010c0010t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0010c0010t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0010c0010t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0010c0010t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0011c0022t0020g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0011c0022t0021g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0011c0039t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0012c0020t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0012c0020t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0013c0026t0005g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0013c0026t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0014c0015t0014g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0014c0015t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0015c0042t0022g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0015c0043t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0016c0018t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0016c0018t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0017c0019t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0017c0019t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0018c0017t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0018c0017t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0019c0016t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0019c0016t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0020c0023t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0020c0023t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0021c0032t0041g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0022c0031t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0023c0049t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0024c0029t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0025c0045t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0026c0041t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0027c0036t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0028c0028t0018g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0029c0046t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0030c0035t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
a0031c0047t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0280 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00140 | hp1 | a0005 | c0004 | t0003 | g0033 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0066 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00323 | hp1 | a0007 | c0006 | t0003 | g0212 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00323 | hp2 | a0002 | c0033 | t0001 | g0062 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00438 | hp1 | a0001 | c0001 | t0009 | g0217 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00609 | hp1 | a0021 | c0032 | t0041 | g0140 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00609 | hp2 | a0002 | c0002 | t0004 | g0284 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00621 | hp1 | a0002 | c0009 | t0002 | g0279 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00621 | hp2 | a0012 | c0020 | t0004 | g0216 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0252 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0270 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00733 | hp2 | a0004 | c0005 | t0016 | g0108 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00741 | hp1 | a0022 | c0031 | t0001 | g0173 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG00741 | hp2 | a0004 | c0005 | t0003 | g0106 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01074 | hp1 | a0002 | c0002 | t0025 | g0067 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0255 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01106 | hp1 | a0004 | c0025 | t0003 | g0111 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01109 | hp1 | a0002 | c0002 | t0029 | g0227 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01109 | hp2 | a0023 | c0049 | t0001 | g0179 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01169 | hp1 | a0024 | c0029 | t0001 | g0060 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0170 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0273 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01258 | hp2 | a0025 | c0045 | t0001 | g0117 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0182 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0262 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01346 | hp1 | a0001 | c0021 | t0001 | g0136 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01346 | hp2 | a0007 | c0006 | t0003 | g0213 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01358 | hp2 | a0008 | c0008 | t0002 | g0021 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01361 | hp1 | a0004 | c0005 | t0003 | g0085 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01361 | hp2 | a0005 | c0004 | t0009 | g0037 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01496 | hp1 | a0011 | c0022 | t0020 | g0045 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0120 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01516 | hp2 | a0013 | c0026 | t0005 | g0025 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01517 | hp2 | a0013 | c0026 | t0005 | g0024 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01884 | hp1 | a0006 | c0011 | t0006 | g0042 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01884 | hp2 | a0014 | c0015 | t0014 | g0289 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01891 | hp1 | a0015 | c0043 | t0023 | g0047 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01891 | hp2 | a0026 | c0041 | t0007 | g0218 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01928 | hp1 | a0002 | c0040 | t0002 | g0266 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01928 | hp2 | a0003 | c0003 | t0003 | g0190 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01943 | hp1 | a0004 | c0005 | t0003 | g0100 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01975 | hp1 | a0001 | c0021 | t0004 | g0137 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0248 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02055 | hp1 | a0002 | c0038 | t0007 | g0011 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02071 | hp2 | a0008 | c0008 | t0002 | g0023 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02074 | hp1 | a0002 | c0009 | t0002 | g0277 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02074 | hp2 | a0001 | c0001 | t0012 | g0159 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02083 | hp2 | a0002 | c0009 | t0002 | g0278 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02145 | hp1 | a0004 | c0014 | t0003 | g0090 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02145 | hp2 | a0016 | c0018 | t0001 | g0206 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02155 | hp1 | a0012 | c0020 | t0004 | g0171 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02165 | hp1 | a0001 | c0001 | t0036 | g0168 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02257 | hp1 | a0005 | c0004 | t0005 | g0028 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02273 | hp1 | a0004 | c0005 | t0005 | g0109 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02273 | hp2 | a0008 | c0008 | t0028 | g0020 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02280 | hp2 | a0009 | c0007 | t0007 | g0012 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02293 | hp2 | a0001 | c0001 | t0011 | g0181 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02523 | hp2 | a0001 | c0024 | t0001 | g0178 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02572 | hp2 | a0027 | c0036 | t0013 | g0285 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0253 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02602 | hp2 | a0003 | c0044 | t0003 | g0183 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02615 | hp1 | a0002 | c0002 | t0004 | g0229 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02615 | hp2 | a0002 | c0002 | t0031 | g0049 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02622 | hp2 | a0005 | c0004 | t0005 | g0034 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02630 | hp1 | a0006 | c0011 | t0013 | g0043 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02630 | hp2 | a0002 | c0002 | t0024 | g0264 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02647 | hp1 | a0002 | c0002 | t0008 | g0274 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02647 | hp2 | a0002 | c0002 | t0017 | g0228 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02683 | hp1 | a0003 | c0003 | t0016 | g0056 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02683 | hp2 | a0004 | c0005 | t0003 | g0107 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02723 | hp1 | a0018 | c0017 | t0010 | g0223 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02723 | hp2 | a0002 | c0002 | t0014 | g0219 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0184 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02735 | hp2 | a0004 | c0025 | t0003 | g0019 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02809 | hp1 | a0005 | c0004 | t0005 | g0003 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02809 | hp2 | a0006 | c0012 | t0006 | g0220 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02818 | hp1 | a0006 | c0012 | t0006 | g0271 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02818 | hp2 | a0018 | c0017 | t0010 | g0222 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02886 | hp1 | a0015 | c0042 | t0022 | g0044 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02886 | hp2 | a0028 | c0028 | t0018 | g0291 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02897 | hp1 | a0005 | c0027 | t0005 | g0009 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02897 | hp2 | a0006 | c0012 | t0006 | g0226 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02922 | hp1 | a0014 | c0015 | t0019 | g0290 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02922 | hp2 | a0003 | c0013 | t0001 | g0006 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02970 | hp1 | a0009 | c0007 | t0007 | g0008 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02970 | hp2 | a0005 | c0004 | t0005 | g0026 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0263 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03017 | hp2 | a0001 | c0001 | t0043 | g0058 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03041 | hp1 | a0009 | c0007 | t0007 | g0013 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03130 | hp1 | a0005 | c0004 | t0005 | g0003 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03130 | hp2 | a0003 | c0013 | t0001 | g0006 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03139 | hp1 | a0005 | c0004 | t0005 | g0029 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03139 | hp2 | a0002 | c0002 | t0030 | g0050 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03209 | hp1 | a0005 | c0004 | t0005 | g0030 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03209 | hp2 | a0019 | c0016 | t0010 | g0224 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03239 | hp2 | a0007 | c0006 | t0003 | g0210 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03453 | hp1 | a0019 | c0016 | t0010 | g0225 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03453 | hp2 | a0006 | c0011 | t0006 | g0039 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03486 | hp1 | a0016 | c0018 | t0001 | g0205 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03486 | hp2 | a0005 | c0048 | t0003 | g0018 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03490 | hp2 | a0007 | c0006 | t0003 | g0287 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03491 | hp2 | a0004 | c0014 | t0003 | g0092 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03492 | hp1 | a0007 | c0006 | t0003 | g0288 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03516 | hp1 | a0005 | c0004 | t0005 | g0027 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03516 | hp2 | a0002 | c0002 | t0004 | g0054 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03540 | hp1 | a0006 | c0012 | t0006 | g0221 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03579 | hp2 | a0009 | c0007 | t0007 | g0008 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0236 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03704 | hp1 | a0004 | c0005 | t0034 | g0087 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03704 | hp2 | a0002 | c0002 | t0008 | g0065 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03831 | hp1 | a0029 | c0046 | t0003 | g0201 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03927 | hp1 | a0002 | c0002 | t0008 | g0063 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03942 | hp1 | a0004 | c0005 | t0003 | g0105 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0256 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04184 | hp1 | a0003 | c0003 | t0003 | g0188 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0249 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0057 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04204 | hp2 | a0005 | c0004 | t0004 | g0015 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04228 | hp1 | a0008 | c0008 | t0001 | g0035 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0254 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18522 | hp1 | a0002 | c0002 | t0026 | g0234 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18522 | hp2 | a0001 | c0001 | t0032 | g0115 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18747 | hp1 | a0002 | c0002 | t0038 | g0235 | EAS | CHB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18906 | hp1 | a0003 | c0013 | t0001 | g0204 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18939 | hp1 | a0007 | c0006 | t0003 | g0209 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18940 | hp1 | a0030 | c0035 | t0001 | g0134 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18942 | hp2 | a0002 | c0002 | t0027 | g0232 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18944 | hp2 | a0003 | c0003 | t0012 | g0199 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18945 | hp1 | a0031 | c0047 | t0002 | g0267 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18945 | hp2 | a0003 | c0003 | t0003 | g0186 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18947 | hp1 | a0003 | c0003 | t0003 | g0191 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18947 | hp2 | a0001 | c0034 | t0001 | g0089 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18948 | hp1 | a0003 | c0003 | t0003 | g0198 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18948 | hp2 | a0001 | c0030 | t0001 | g0139 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18952 | hp1 | a0008 | c0008 | t0002 | g0036 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18957 | hp1 | a0003 | c0003 | t0003 | g0207 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18960 | hp2 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18963 | hp1 | a0002 | c0002 | t0008 | g0242 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18963 | hp2 | a0001 | c0001 | t0040 | g0141 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18964 | hp1 | a0002 | c0009 | t0002 | g0276 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18966 | hp2 | a0003 | c0003 | t0003 | g0196 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18967 | hp2 | a0002 | c0002 | t0008 | g0243 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18971 | hp1 | a0002 | c0002 | t0008 | g0051 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18971 | hp2 | a0003 | c0003 | t0012 | g0200 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18973 | hp2 | a0001 | c0001 | t0009 | g0155 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18992 | hp1 | a0003 | c0003 | t0015 | g0197 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18994 | hp1 | a0002 | c0009 | t0002 | g0275 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18994 | hp2 | a0001 | c0001 | t0009 | g0146 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18998 | hp1 | a0004 | c0005 | t0005 | g0104 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18999 | hp1 | a0008 | c0008 | t0002 | g0022 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19002 | hp1 | a0011 | c0039 | t0002 | g0241 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19003 | hp1 | a0002 | c0002 | t0004 | g0233 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19003 | hp2 | a0010 | c0010 | t0001 | g0175 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19004 | hp1 | a0010 | c0010 | t0001 | g0131 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19004 | hp2 | a0003 | c0003 | t0003 | g0194 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19006 | hp1 | a0003 | c0003 | t0042 | g0195 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19009 | hp2 | a0001 | c0024 | t0001 | g0164 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19011 | hp2 | a0001 | c0001 | t0039 | g0098 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19030 | hp1 | a0005 | c0004 | t0015 | g0017 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19030 | hp2 | a0009 | c0007 | t0007 | g0014 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19043 | hp1 | a0006 | c0011 | t0006 | g0041 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19043 | hp2 | a0009 | c0007 | t0007 | g0016 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19058 | hp2 | a0020 | c0023 | t0002 | g0258 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19063 | hp1 | a0005 | c0004 | t0001 | g0031 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19065 | hp1 | a0010 | c0010 | t0001 | g0132 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19072 | hp2 | a0003 | c0003 | t0003 | g0189 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19080 | hp1 | a0020 | c0023 | t0002 | g0257 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19080 | hp2 | a0003 | c0003 | t0003 | g0282 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19083 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19083 | hp2 | a0010 | c0010 | t0001 | g0154 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0203 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | ASW | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA20129 | hp2 | a0002 | c0002 | t0037 | g0294 | AFR | ASW | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA20905 | hp1 | a0003 | c0003 | t0003 | g0202 | SAS | GIH | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA20905 | hp2 | a0003 | c0003 | t0002 | g0286 | SAS | GIH | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01123 | hp1 | a0004 | c0014 | t0035 | g0101 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02559 | hp1 | a0017 | c0019 | t0006 | g0083 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG02559 | hp2 | a0005 | c0004 | t0044 | g0032 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0292 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG03471 | hp2 | a0004 | c0005 | t0033 | g0048 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
HG06807 | hp2 | a0006 | c0037 | t0006 | g0040 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA18955 | hp2 | a0003 | c0003 | t0001 | g0192 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA20300 | hp1 | a0011 | c0022 | t0021 | g0046 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA20300 | hp2 | a0007 | c0006 | t0003 | g0211 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
NA21309 | hp2 | a0017 | c0019 | t0006 | g0112 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0010 | REF | REF | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
homoSapiens | grch38p0 | a0004 | c0005 | t0003 | g0093 | REF | REF | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:45867602 | C | A | 1 | a0012 | 2 | HG00621.hp2 HG02155.hp1 |
missense_variant | MODERATE | c.6372G>T | p.Met2124Ile | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 37/44 | 6462/12688 | 6372/7740 | 2124/2579 | chr18 | 45867602 | |||
chr18:45876331 | C | T | 3 | a0011 a0018 a0019 |
6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.5954G>A | p.Arg1985Gln | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/44 | 6044/12688 | 5954/7740 | 1985/2579 | chr18 | 45876331 | |||
chr18:45876332 | G | A | 1 | a0011 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.5953C>T | p.Arg1985Trp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/44 | 6043/12688 | 5953/7740 | 1985/2579 | chr18 | 45876332 | |||
chr18:45879202 | T | C | 1 | a0028 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.5680A>G | p.Ile1894Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/44 | 5770/12688 | 5680/7740 | 1894/2579 | chr18 | 45879202 | |||
chr18:45880124 | T | A | 1 | a0010 | 4 | NA19003.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
missense_variant | MODERATE | c.5618A>T | p.Glu1873Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5708/12688 | 5618/7740 | 1873/2579 | chr18 | 45880124 | |||
chr18:45880151 | C | T | 3 | a0006 a0017 a0027 |
12 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
missense_variant | MODERATE | c.5591G>A | p.Ser1864Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5681/12688 | 5591/7740 | 1864/2579 | chr18 | 45880151 | |||
chr18:45884648 | T | C | 1 | a0020 | 2 | NA19058.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.5273A>G | p.Asn1758Ser | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/44 | 5363/12688 | 5273/7740 | 1758/2579 | chr18 | 45884648 | |||
chr18:45889889 | G | A | 1 | a0026 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.4861C>T | p.Arg1621Trp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/44 | 4951/12688 | 4861/7740 | 1621/2579 | chr18 | 45889889 | |||
chr18:45901110 | G | A | 12 | a0002 a0006 a0009 others(9): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
missense_variant | MODERATE | c.4532C>T | p.Ala1511Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/44 | 4622/12688 | 4532/7740 | 1511/2579 | chr18 | 45901110 | |||
chr18:45915596 | C | T | 1 | a0019 | 2 | HG03209.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.3608G>A | p.Arg1203Gln | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/44 | 3698/12688 | 3608/7740 | 1203/2579 | chr18 | 45915596 | |||
chr18:45916098 | T | C | 1 | a0016 | 2 | HG02145.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.3493A>G | p.Ile1165Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/44 | 3583/12688 | 3493/7740 | 1165/2579 | chr18 | 45916098 | |||
chr18:45916200 | T | C | 1 | a0030 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.3391A>G | p.Ile1131Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/44 | 3481/12688 | 3391/7740 | 1131/2579 | chr18 | 45916200 | |||
chr18:45916574 | G | A | 1 | a0007 | 7 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(4): Show |
missense_variant | MODERATE | c.3248C>T | p.Ser1083Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/44 | 3338/12688 | 3248/7740 | 1083/2579 | chr18 | 45916574 | |||
chr18:45917745 | A | G | 10 | a0001 a0010 a0012 others(7): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
missense_variant | MODERATE | c.3173T>C | p.Val1058Ala | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/44 | 3263/12688 | 3173/7740 | 1058/2579 | chr18 | 45917745 | |||
chr18:45922441 | T | C | 1 | a0015 | 2 | HG01891.hp1 HG02886.hp1 |
missense_variant | MODERATE | c.2998A>G | p.Met1000Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/44 | 3088/12688 | 2998/7740 | 1000/2579 | chr18 | 45922441 | |||
chr18:45922528 | A | C | 1 | a0014 | 2 | HG01884.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.2911T>G | p.Leu971Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/44 | 3001/12688 | 2911/7740 | 971/2579 | chr18 | 45922528 | |||
chr18:45928890 | C | G | 4 | a0003 a0007 a0016 others(1): Show |
36 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(33): Show |
missense_variant | MODERATE | c.2532G>C | p.Glu844Asp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/44 | 2622/12688 | 2532/7740 | 844/2579 | chr18 | 45928890 | |||
chr18:45939636 | A | G | 2 | a0018 a0019 |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
missense_variant | MODERATE | c.2063T>C | p.Phe688Ser | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/44 | 2153/12688 | 2063/7740 | 688/2579 | chr18 | 45939636 | |||
chr18:45944031 | T | C | 1 | a0025 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1766A>G | p.Gln589Arg | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/44 | 1856/12688 | 1766/7740 | 589/2579 | chr18 | 45944031 | |||
chr18:45946731 | C | T | 1 | a0021 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1609G>A | p.Glu537Lys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/44 | 1699/12688 | 1609/7740 | 537/2579 | chr18 | 45946731 | |||
chr18:45949563 | G | A | 1 | a0029 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1418C>T | p.Pro473Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/44 | 1508/12688 | 1418/7740 | 473/2579 | chr18 | 45949563 | |||
chr18:45951220 | C | T | 1 | a0013 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.1271G>A | p.Ser424Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/44 | 1361/12688 | 1271/7740 | 424/2579 | chr18 | 45951220 | |||
chr18:45954632 | T | C | 1 | a0031 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.770A>G | p.Lys257Arg | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 860/12688 | 770/7740 | 257/2579 | chr18 | 45954632 | |||
chr18:45954662 | G | A | 1 | a0008 | 6 | HG01358.hp2 HG02071.hp2 HG02273.hp2 others(3): Show |
missense_variant | MODERATE | c.740C>T | p.Pro247Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 830/12688 | 740/7740 | 247/2579 | chr18 | 45954662 | |||
chr18:45954858 | T | C | 4 | a0005 a0008 a0009 others(1): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
missense_variant | MODERATE | c.544A>G | p.Lys182Glu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 634/12688 | 544/7740 | 182/2579 | chr18 | 45954858 | |||
chr18:45954978 | C | T | 1 | a0022 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.424G>A | p.Glu142Lys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 514/12688 | 424/7740 | 142/2579 | chr18 | 45954978 | |||
chr18:45955139 | A | C | 1 | a0024 | 1 | HG01169.hp1 | stop_gained | HIGH | c.263T>G | p.Leu88* | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 353/12688 | 263/7740 | 88/2579 | chr18 | 45955139 | |||
chr18:45955251 | G | C | 1 | a0023 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.151C>G | p.Leu51Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 241/12688 | 151/7740 | 51/2579 | chr18 | 45955251 | |||
chr18:45955298 | C | T | 2 | a0014 a0028 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.104G>A | p.Ser35Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 194/12688 | 104/7740 | 35/2579 | chr18 | 45955298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:45852586 | A | G | 1 | a0006c0037 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.7621T>C | p.Leu2541Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 7711/12688 | 7621/7740 | 2541/2579 | chr18 | 45852586 | |||
chr18:45857927 | G | A | 1 | a0001c0034 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.7368C>T | p.Leu2456Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/44 | 7458/12688 | 7368/7740 | 2456/2579 | chr18 | 45857927 | |||
chr18:45866897 | C | T | 1 | a0004c0014 | 3 | HG01123.hp1 HG02145.hp1 HG03491.hp2 |
synonymous_variant | LOW | c.6522G>A | p.Pro2174Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/44 | 6612/12688 | 6522/7740 | 2174/2579 | chr18 | 45866897 | |||
chr18:45866903 | G | A | 2 | a0011c0022 a0015c0043 |
3 | HG01496.hp1 HG01891.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.6516C>T | p.Tyr2172Tyr | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/44 | 6606/12688 | 6516/7740 | 2172/2579 | chr18 | 45866903 | |||
chr18:45879182 | A | G | 2 | a0003c0013 a0016c0018 |
5 | HG02145.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.5700T>C | p.Phe1900Phe | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/44 | 5790/12688 | 5700/7740 | 1900/2579 | chr18 | 45879182 | |||
chr18:45880126 | G | A | 1 | a0010c0010 | 4 | NA19003.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
synonymous_variant | LOW | c.5616C>T | p.Thr1872Thr | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5706/12688 | 5616/7740 | 1872/2579 | chr18 | 45880126 | |||
chr18:45880159 | G | A | 1 | a0011c0022 | 2 | HG01496.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.5583C>T | p.Cys1861Cys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5673/12688 | 5583/7740 | 1861/2579 | chr18 | 45880159 | |||
chr18:45880198 | G | C | 1 | a0002c0040 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.5544C>G | p.Pro1848Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5634/12688 | 5544/7740 | 1848/2579 | chr18 | 45880198 | |||
chr18:45884692 | G | A | 1 | a0002c0009 | 5 | HG00621.hp1 HG02074.hp1 HG02083.hp2 others(2): Show |
synonymous_variant | LOW | c.5229C>T | p.Phe1743Phe | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/44 | 5319/12688 | 5229/7740 | 1743/2579 | chr18 | 45884692 | |||
chr18:45901013 | C | T | 1 | a0011c0022 | 2 | HG01496.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.4629G>A | p.Leu1543Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/44 | 4719/12688 | 4629/7740 | 1543/2579 | chr18 | 45901013 | |||
chr18:45910637 | G | A | 12 | a0002c0002 a0002c0009 a0002c0033 others(9): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
synonymous_variant | LOW | c.4089C>T | p.His1363His | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/44 | 4179/12688 | 4089/7740 | 1363/2579 | chr18 | 45910637 | |||
chr18:45916155 | A | G | 3 | a0011c0022 a0015c0042 a0015c0043 |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.3436T>C | p.Leu1146Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/44 | 3526/12688 | 3436/7740 | 1146/2579 | chr18 | 45916155 | |||
chr18:45916543 | G | A | 1 | a0001c0021 | 2 | HG01346.hp1 HG01975.hp1 |
synonymous_variant | LOW | c.3279C>T | p.Ser1093Ser | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/44 | 3369/12688 | 3279/7740 | 1093/2579 | chr18 | 45916543 | |||
chr18:45930715 | G | A | 1 | a0003c0044 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2373C>T | p.Asp791Asp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/44 | 2463/12688 | 2373/7740 | 791/2579 | chr18 | 45930715 | |||
chr18:45943175 | A | G | 1 | a0002c0033 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1929T>C | p.Ile643Ile | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/44 | 2019/12688 | 1929/7740 | 643/2579 | chr18 | 45943175 | |||
chr18:45949520 | G | A | 1 | a0001c0024 | 2 | HG02523.hp2 NA19009.hp2 |
synonymous_variant | LOW | c.1461C>T | p.Pro487Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/44 | 1551/12688 | 1461/7740 | 487/2579 | chr18 | 45949520 | |||
chr18:45949582 | G | A | 1 | a0004c0025 | 2 | HG01106.hp1 HG02735.hp2 |
synonymous_variant | LOW | c.1399C>T | p.Leu467Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/44 | 1489/12688 | 1399/7740 | 467/2579 | chr18 | 45949582 | |||
chr18:45955021 | A | G | 1 | a0001c0030 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.381T>C | p.Asn127Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 471/12688 | 381/7740 | 127/2579 | chr18 | 45955021 | |||
chr18:45955096 | G | A | 1 | a0005c0048 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.306C>T | p.Pro102Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 396/12688 | 306/7740 | 102/2579 | chr18 | 45955096 | |||
chr18:45967222 | C | T | 1 | a0005c0027 | 1 | HG02897.hp1 | synonymous_variant | LOW | c.18G>A | p.Lys6Lys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/44 | 108/12688 | 18/7740 | 6/2579 | chr18 | 45967222 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:45847656 | T | C | 1 | a0021c0032t0041 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4811A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4811 | chr18 | 45847656 | ||||||
chr18:45847658 | G | A | 25 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(22): Show |
85 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4809C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4809 | chr18 | 45847658 | ||||||
chr18:45847953 | G | A | 9 | a0001c0001t0005 a0001c0001t0032 a0002c0002t0017 others(6): Show |
20 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4514C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4514 | chr18 | 45847953 | ||||||
chr18:45847979 | C | T | 1 | a0014c0015t0019 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4488G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4488 | chr18 | 45847979 | ||||||
chr18:45847992 | A | AT | 45 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(42): Show |
122 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*4474dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4474 | chr18 | 45847992 | ||||||
chr18:45848500 | T | C | 1 | a0011c0022t0021 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3967A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3967 | chr18 | 45848500 | ||||||
chr18:45848584 | C | T | 4 | a0011c0022t0020 a0011c0022t0021 a0015c0042t0022 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3883G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3883 | chr18 | 45848584 | ||||||
chr18:45848647 | C | T | 1 | a0001c0001t0039 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3820G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3820 | chr18 | 45848647 | ||||||
chr18:45848971 | T | C | 42 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(39): Show |
119 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3496A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3496 | chr18 | 45848971 | ||||||
chr18:45849061 | G | A | 1 | a0002c0002t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3406C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3406 | chr18 | 45849061 | ||||||
chr18:45849081 | C | CA | 8 | a0001c0001t0009 a0003c0003t0042 a0005c0004t0009 others(5): Show |
11 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3385dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3385 | chr18 | 45849081 | ||||||
chr18:45849081 | CA | C | 23 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0032 others(20): Show |
64 | HG00609.hp2 HG00621.hp2 HG01071.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3385delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3385 | chr18 | 45849081 | ||||||
chr18:45849081 | CAA | C | 15 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0024 others(12): Show |
64 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3384_*3385delTT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3384 | chr18 | 45849081 | ||||||
chr18:45849107 | T | G | 1 | a0002c0002t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3360A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3360 | chr18 | 45849107 | ||||||
chr18:45849218 | T | A | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(77): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*3249A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3249 | chr18 | 45849218 | ||||||
chr18:45849222 | C | T | 1 | a0002c0002t0026 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3245G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3245 | chr18 | 45849222 | ||||||
chr18:45849298 | A | C | 1 | a0002c0002t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3169 | chr18 | 45849298 | ||||||
chr18:45849315 | G | A | 1 | a0008c0008t0028 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3152C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3152 | chr18 | 45849315 | ||||||
chr18:45849335 | C | T | 2 | a0018c0017t0010 a0019c0016t0010 |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3132G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3132 | chr18 | 45849335 | ||||||
chr18:45849372 | A | G | 45 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0032 others(42): Show |
121 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*3095T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3095 | chr18 | 45849372 | ||||||
chr18:45849523 | T | C | 1 | a0002c0002t0031 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2944A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2944 | chr18 | 45849523 | ||||||
chr18:45849607 | A | G | 1 | a0002c0002t0037 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2860 | chr18 | 45849607 | ||||||
chr18:45849741 | C | G | 2 | a0011c0022t0020 a0011c0022t0021 |
2 | HG01496.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2726G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2726 | chr18 | 45849741 | ||||||
chr18:45850001 | C | T | 36 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(33): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2466G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2466 | chr18 | 45850001 | ||||||
chr18:45850174 | G | A | 40 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0032 others(37): Show |
116 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2293C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2293 | chr18 | 45850174 | ||||||
chr18:45850225 | C | A | 40 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0032 others(37): Show |
116 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2242G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2242 | chr18 | 45850225 | ||||||
chr18:45850238 | G | A | 1 | a0002c0002t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2229C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2229 | chr18 | 45850238 | ||||||
chr18:45850357 | C | T | 1 | a0001c0001t0036 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2110G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2110 | chr18 | 45850357 | ||||||
chr18:45850383 | G | A | 3 | a0001c0001t0043 a0003c0003t0016 a0004c0005t0016 |
3 | HG00733.hp2 HG02683.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2084 | chr18 | 45850383 | ||||||
chr18:45850444 | C | A | 40 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0032 others(37): Show |
116 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2023G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2023 | chr18 | 45850444 | ||||||
chr18:45850878 | A | G | 1 | a0002c0002t0024 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 1589 | chr18 | 45850878 | ||||||
chr18:45850951 | C | T | 1 | a0004c0014t0035 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1516G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 1516 | chr18 | 45850951 | ||||||
chr18:45851468 | T | C | 1 | a0005c0004t0044 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 999 | chr18 | 45851468 | ||||||
chr18:45851602 | G | A | 1 | a0002c0002t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 865 | chr18 | 45851602 | ||||||
chr18:45851772 | G | C | 2 | a0002c0002t0030 a0002c0002t0031 |
2 | HG02615.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*695C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 695 | chr18 | 45851772 | ||||||
chr18:45851835 | C | T | 8 | a0001c0001t0005 a0002c0002t0017 a0004c0005t0005 others(5): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*632G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 632 | chr18 | 45851835 | ||||||
chr18:45851885 | C | T | 1 | a0028c0028t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 582 | chr18 | 45851885 | ||||||
chr18:45852068 | G | A | 1 | a0001c0001t0032 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 399 | chr18 | 45852068 | ||||||
chr18:45852197 | C | T | 4 | a0011c0022t0020 a0011c0022t0021 a0015c0042t0022 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*270G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 270 | chr18 | 45852197 | ||||||
chr18:45852280 | A | AAC | 10 | a0001c0001t0011 a0002c0002t0014 a0002c0038t0007 others(7): Show |
17 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*185_*186dupGT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 186 | chr18 | 45852280 | ||||||
chr18:45852280 | A | AACAC | 6 | a0006c0011t0006 a0006c0011t0013 a0006c0012t0006 others(3): Show |
12 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*183_*186dupGTGT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 186 | chr18 | 45852280 | ||||||
chr18:45852280 | A | AACACAC | 8 | a0001c0001t0005 a0002c0002t0017 a0004c0005t0005 others(5): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*181_*186dupGTGTGT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 186 | chr18 | 45852280 | ||||||
chr18:45852301 | A | C | 3 | a0011c0022t0020 a0011c0022t0021 a0015c0042t0022 |
3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*166T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 166 | chr18 | 45852301 | ||||||
chr18:45852303 | A | C | 4 | a0004c0005t0033 a0011c0022t0020 a0011c0022t0021 others(1): Show |
4 | HG01496.hp1 HG02886.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*164T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 164 | chr18 | 45852303 | ||||||
chr18:45852327 | C | T | 44 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0032 others(41): Show |
120 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*140G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 140 | chr18 | 45852327 | ||||||
chr18:45852393 | A | C | 21 | a0001c0001t0005 a0002c0002t0014 a0002c0002t0017 others(18): Show |
43 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*74T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 74 | chr18 | 45852393 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:45852660 | C | T | 28 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0088 others(25): Show |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.7558-11G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45852660 | |||||||
chr18:45852781 | G | A | 1 | a0005c0004t0044g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7558-132C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45852781 | |||||||
chr18:45852854 | G | A | 11 | a0002c0002t0014g0219 a0002c0038t0007g0011 a0009c0007t0007g0008 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.7558-205C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45852854 | |||||||
chr18:45853005 | G | A | 2 | a0001c0001t0001g0061 a0024c0029t0001g0060 |
2 | HG01169.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7558-356C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853005 | |||||||
chr18:45853138 | G | C | 1 | a0008c0008t0002g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.7558-489C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853138 | |||||||
chr18:45853264 | C | G | 11 | a0002c0002t0014g0219 a0002c0038t0007g0011 a0009c0007t0007g0008 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.7558-615G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853264 | |||||||
chr18:45853436 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7558-787T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853436 | |||||||
chr18:45853581 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0167 others(2): Show |
5 | NA18948.hp2 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.7558-932G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853581 | |||||||
chr18:45853582 | C | G | 69 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0032g0115 others(66): Show |
72 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.7558-933G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853582 | |||||||
chr18:45853709 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7558-1060C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853709 | |||||||
chr18:45853787 | G | A | 4 | a0002c0002t0014g0219 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.7558-1138C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853787 | |||||||
chr18:45854000 | A | G | 1 | a0010c0010t0001g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.7558-1351T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854000 | |||||||
chr18:45854013 | C | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.7558-1364G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854013 | |||||||
chr18:45854029 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0169 |
2 | NA19010.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.7558-1380T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854029 | |||||||
chr18:45854190 | T | G | 2 | a0003c0003t0012g0199 a0003c0003t0012g0200 |
2 | NA18944.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.7557+1383A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854190 | |||||||
chr18:45854218 | G | T | 1 | a0005c0004t0044g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7557+1355C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854218 | |||||||
chr18:45854282 | G | A | 1 | a0001c0001t0032g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7557+1291C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854282 | |||||||
chr18:45854338 | T | C | 1 | a0005c0004t0044g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7557+1235A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854338 | |||||||
chr18:45854559 | CA | C | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0161 others(3): Show |
6 | HG01109.hp2 NA18747.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.7557+1013delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854559 | |||||||
chr18:45854642 | T | C | 1 | a0010c0010t0001g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.7557+931A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854642 | |||||||
chr18:45854703 | A | T | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7557+870T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854703 | |||||||
chr18:45854705 | T | A | 2 | a0002c0002t0004g0054 a0002c0002t0004g0229 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7557+868A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854705 | |||||||
chr18:45854791 | T | C | 2 | a0002c0002t0001g0066 a0002c0033t0001g0062 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.7557+782A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854791 | |||||||
chr18:45854926 | C | T | 1 | a0003c0013t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7557+647G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854926 | |||||||
chr18:45854956 | T | C | 76 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(73): Show |
79 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.7557+617A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854956 | |||||||
chr18:45855162 | G | A | 3 | a0002c0002t0002g0248 a0002c0002t0002g0249 a0002c0002t0002g0262 |
3 | HG01261.hp2 HG01981.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.7557+411C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45855162 | |||||||
chr18:45855558 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0138 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7557+15T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45855558 | |||||||
chr18:45855701 | G | A | 3 | a0002c0002t0014g0219 a0014c0015t0014g0289 a0014c0015t0019g0290 |
3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.7443-14C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45855701 | |||||||
chr18:45855768 | C | T | 1 | a0008c0008t0002g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.7443-81G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45855768 | |||||||
chr18:45855773 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.7443-86T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45855773 | |||||||
chr18:45856094 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7443-407A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856094 | |||||||
chr18:45856190 | C | A | 18 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(15): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.7443-503G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856190 | |||||||
chr18:45856256 | T | C | 41 | a0001c0001t0005g0099 a0002c0002t0014g0219 a0002c0002t0017g0228 others(38): Show |
43 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.7443-569A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856256 | |||||||
chr18:45856666 | T | C | 1 | a0010c0010t0001g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.7443-979A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856666 | |||||||
chr18:45856699 | C | T | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7443-1012G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856699 | |||||||
chr18:45856735 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0091 others(14): Show |
17 | HG00438.hp1 HG01081.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.7443-1048T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856735 | |||||||
chr18:45856792 | A | AT | 18 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(15): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.7442+1060dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856792 | |||||||
chr18:45856992 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7442+861C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856992 | |||||||
chr18:45856997 | C | T | 17 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0091 others(14): Show |
17 | HG00438.hp1 HG01081.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.7442+856G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856997 | |||||||
chr18:45857021 | C | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0152 others(6): Show |
12 | HG02083.hp1 HG02523.hp2 HG03834.hp1 others(9): Show |
intron_variant | MODIFIER | c.7442+832G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857021 | |||||||
chr18:45857099 | G | GTTTA | 3 | a0008c0008t0001g0035 a0013c0026t0005g0024 a0013c0026t0005g0025 |
3 | HG01516.hp2 HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.7442+750_7442+753d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857099 | |||||||
chr18:45857099 | GTTTA | G | 75 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(72): Show |
78 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.7442+750_7442+753d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857099 | |||||||
chr18:45857281 | T | C | 70 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(67): Show |
73 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.7442+572A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857281 | |||||||
chr18:45857403 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.7442+450C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857403 | |||||||
chr18:45857529 | C | A | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7442+324G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857529 | |||||||
chr18:45857587 | C | A | 1 | a0015c0042t0022g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7442+266G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857587 | |||||||
chr18:45857661 | A | G | 1 | a0002c0002t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7442+192T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857661 | |||||||
chr18:45857760 | C | T | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7442+93G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857760 | |||||||
chr18:45858191 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.7227-123G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858191 | |||||||
chr18:45858196 | G | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0004g0059 others(4): Show |
7 | HG01175.hp1 HG01243.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.7227-128C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858196 | |||||||
chr18:45858228 | G | A | 1 | a0002c0002t0003g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7227-160C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858228 | |||||||
chr18:45858250 | C | T | 1 | a0002c0002t0002g0238 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.7227-182G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858250 | |||||||
chr18:45858471 | T | A | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7226+95A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858471 | |||||||
chr18:45858871 | A | AT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0079 others(18): Show |
22 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.7010-90dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45858871 | |||||||
chr18:45858873 | T | C | 1 | a0005c0004t0005g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7010-91A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45858873 | |||||||
chr18:45859145 | T | A | 2 | a0002c0002t0004g0054 a0002c0002t0004g0229 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7010-363A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859145 | |||||||
chr18:45859318 | C | T | 1 | a0006c0012t0006g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7010-536G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859318 | |||||||
chr18:45859469 | A | G | 2 | a0013c0026t0005g0024 a0013c0026t0005g0025 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.7009+635T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859469 | |||||||
chr18:45859933 | ATC | A | 7 | a0007c0006t0003g0209 a0007c0006t0003g0210 a0007c0006t0003g0211 others(4): Show |
7 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.7009+169_7009+170d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859933 | |||||||
chr18:45859937 | T | G | 7 | a0007c0006t0003g0209 a0007c0006t0003g0210 a0007c0006t0003g0211 others(4): Show |
7 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.7009+167A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859937 | |||||||
chr18:45859963 | C | T | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7009+141G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859963 | |||||||
chr18:45860521 | G | T | 1 | a0001c0001t0005g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6767-175C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860521 | |||||||
chr18:45860527 | G | A | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-181C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860527 | |||||||
chr18:45860584 | G | A | 3 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 |
3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-238C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860584 | |||||||
chr18:45860597 | ATACT | A | 18 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(15): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6767-255_6767-252d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860597 | |||||||
chr18:45860641 | C | T | 1 | a0006c0011t0013g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6767-295G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860641 | |||||||
chr18:45860703 | G | A | 71 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0032g0115 others(68): Show |
74 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.6767-357C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860703 | |||||||
chr18:45860711 | C | T | 1 | a0002c0002t0002g0238 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.6767-365G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860711 | |||||||
chr18:45860720 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6767-374A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860720 | |||||||
chr18:45860762 | C | T | 3 | a0002c0002t0014g0219 a0014c0015t0014g0289 a0014c0015t0019g0290 |
3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.6767-416G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860762 | |||||||
chr18:45860900 | C | T | 1 | a0004c0014t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6767-554G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860900 | |||||||
chr18:45860907 | G | C | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6767-561C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860907 | |||||||
chr18:45861353 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6767-1007G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861353 | |||||||
chr18:45861435 | T | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.6767-1089A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861435 | |||||||
chr18:45861613 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6767-1267A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861613 | |||||||
chr18:45861793 | G | C | 1 | a0026c0041t0007g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6767-1447C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861793 | |||||||
chr18:45861910 | A | G | 1 | a0003c0044t0003g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6767-1564T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861910 | |||||||
chr18:45862111 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0138 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.6767-1765C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862111 | |||||||
chr18:45862156 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6767-1810A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862156 | |||||||
chr18:45862319 | T | C | 2 | a0002c0002t0030g0050 a0002c0002t0031g0049 |
2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.6767-1973A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862319 | |||||||
chr18:45862366 | C | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-2020G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862366 | |||||||
chr18:45862688 | C | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-2342G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862688 | |||||||
chr18:45862877 | C | T | 1 | a0005c0004t0044g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6767-2531G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862877 | |||||||
chr18:45862920 | T | C | 76 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(73): Show |
79 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.6767-2574A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862920 | |||||||
chr18:45863000 | T | G | 1 | a0006c0012t0006g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6766+2615A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863000 | |||||||
chr18:45863242 | C | G | 2 | a0002c0002t0029g0227 a0015c0042t0022g0044 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6766+2373G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863242 | |||||||
chr18:45863253 | T | C | 3 | a0001c0001t0001g0125 a0001c0021t0001g0136 a0001c0021t0004g0137 |
3 | HG01346.hp1 HG01975.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.6766+2362A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863253 | |||||||
chr18:45863816 | G | C | 1 | a0001c0034t0001g0089 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.6766+1799C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863816 | |||||||
chr18:45863888 | T | G | 1 | a0031c0047t0002g0267 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6766+1727A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863888 | |||||||
chr18:45864067 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0128 |
4 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.6766+1548A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864067 | |||||||
chr18:45864099 | A | C | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6766+1516T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864099 | |||||||
chr18:45864169 | C | A | 1 | a0002c0002t0026g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6766+1446G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864169 | |||||||
chr18:45864197 | C | T | 4 | a0001c0001t0003g0095 a0004c0025t0003g0019 a0004c0025t0003g0111 others(1): Show |
4 | HG01106.hp1 HG02280.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.6766+1418G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864197 | |||||||
chr18:45864332 | C | T | 18 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(15): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6766+1283G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864332 | |||||||
chr18:45864337 | G | C | 7 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.6766+1278C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864337 | |||||||
chr18:45864654 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.6766+961G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864654 | |||||||
chr18:45864892 | T | G | 70 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(67): Show |
73 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.6766+723A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864892 | |||||||
chr18:45864921 | T | C | 16 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0004g0057 others(13): Show |
16 | HG00609.hp2 HG00621.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.6766+694A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864921 | |||||||
chr18:45864989 | C | T | 1 | a0001c0001t0012g0159 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.6766+626G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864989 | |||||||
chr18:45865242 | T | G | 1 | a0002c0002t0029g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6766+373A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865242 | |||||||
chr18:45865267 | G | A | 1 | a0002c0002t0008g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6766+348C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865267 | |||||||
chr18:45865293 | G | A | 18 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(15): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6766+322C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865293 | |||||||
chr18:45865377 | C | T | 72 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(69): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.6766+238G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865377 | |||||||
chr18:45865765 | C | CA | 13 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0081 others(10): Show |
13 | HG00735.hp1 HG01175.hp1 HG01243.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.6622-7dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | |||||||
chr18:45865765 | C | CAAAAAAA others(3): Show |
1 | a0015c0043t0023g0047 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.6622-16_6622-7dupT others(9): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | |||||||
chr18:45865765 | C | CAAAAAAA others(5): Show |
2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.6622-18_6622-7dupT others(11): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | |||||||
chr18:45865765 | CA | C | 72 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0004g0075 others(69): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
splice_region_variant&intron_variant | LOW | c.6622-7delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | |||||||
chr18:45865851 | G | C | 72 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(69): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.6622-92C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865851 | |||||||
chr18:45866006 | A | G | 2 | a0002c0002t0029g0227 a0015c0042t0022g0044 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6622-247T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866006 | |||||||
chr18:45866122 | C | CT | 112 | a0001c0001t0001g0097 a0001c0001t0002g0174 a0001c0001t0005g0099 others(109): Show |
117 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.6622-364dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866122 | |||||||
chr18:45866177 | T | C | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6622-418A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866177 | |||||||
chr18:45866183 | G | A | 7 | a0002c0038t0007g0011 a0009c0007t0007g0008 a0009c0007t0007g0012 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6622-424C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866183 | |||||||
chr18:45866322 | T | C | 10 | a0002c0002t0002g0245 a0002c0002t0002g0247 a0002c0002t0002g0250 others(7): Show |
10 | HG00639.hp2 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.6621+476A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866322 | |||||||
chr18:45866364 | G | A | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6621+434C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866364 | |||||||
chr18:45866467 | C | T | 1 | a0001c0024t0001g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6621+331G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866467 | |||||||
chr18:45866541 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6621+257A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866541 | |||||||
chr18:45866769 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.6621+29A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866769 | |||||||
chr18:45867257 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.6412-250G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 37/43 | chr18 | 45867257 | |||||||
chr18:45867497 | G | A | 1 | a0002c0002t0004g0284 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6411+66C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 37/43 | chr18 | 45867497 | |||||||
chr18:45868324 | C | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.6226-576G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868324 | |||||||
chr18:45868339 | C | CTT | 7 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.6226-593_6226-592d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868339 | |||||||
chr18:45868390 | C | T | 1 | a0003c0003t0003g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.6226-642G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868390 | |||||||
chr18:45868391 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6226-643C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868391 | |||||||
chr18:45868400 | C | T | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6226-652G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868400 | |||||||
chr18:45868423 | C | T | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6226-675G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868423 | |||||||
chr18:45868424 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6226-676C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868424 | |||||||
chr18:45868660 | C | T | 18 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(15): Show |
19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6226-912G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868660 | |||||||
chr18:45868665 | G | A | 1 | a0008c0008t0002g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.6226-917C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868665 | |||||||
chr18:45868671 | T | C | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6226-923A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868671 | |||||||
chr18:45868935 | G | A | 68 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0002c0002t0002g0002 others(65): Show |
71 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.6226-1187C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868935 | |||||||
chr18:45868954 | C | T | 1 | a0002c0002t0029g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6226-1206G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868954 | |||||||
chr18:45869047 | T | A | 1 | a0005c0004t0015g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6226-1299A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869047 | |||||||
chr18:45869054 | C | CA | 19 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0079 others(16): Show |
20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.6226-1307dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869054 | |||||||
chr18:45869183 | T | C | 7 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.6225+1384A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869183 | |||||||
chr18:45869266 | G | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0074 others(72): Show |
78 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.6225+1301C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869266 | |||||||
chr18:45869353 | T | C | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6225+1214A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869353 | |||||||
chr18:45869741 | T | A | 1 | a0015c0043t0023g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6225+826A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869741 | |||||||
chr18:45869928 | TA | T | 82 | a0001c0001t0001g0125 a0001c0001t0001g0149 a0001c0001t0001g0157 others(79): Show |
85 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.6225+638delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869928 | |||||||
chr18:45870082 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6225+485G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870082 | |||||||
chr18:45870104 | T | A | 7 | a0002c0002t0017g0228 a0005c0004t0005g0003 a0005c0004t0005g0026 others(4): Show |
8 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.6225+463A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870104 | |||||||
chr18:45870242 | T | A | 1 | a0001c0001t0039g0098 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6225+325A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870242 | |||||||
chr18:45870386 | T | C | 73 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(70): Show |
76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.6225+181A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870386 | |||||||
chr18:45870393 | G | A | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6225+174C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870393 | |||||||
chr18:45870776 | T | C | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-34A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870776 | |||||||
chr18:45870779 | G | T | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-37C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870779 | |||||||
chr18:45870780 | G | T | 1 | a0005c0004t0005g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6050-38C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870780 | |||||||
chr18:45870788 | T | TA | 7 | a0002c0038t0007g0011 a0009c0007t0007g0008 a0009c0007t0007g0012 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6050-47dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870788 | |||||||
chr18:45870788 | TA | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.6050-47delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870788 | |||||||
chr18:45871002 | C | T | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6050-260G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871002 | |||||||
chr18:45871419 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.6050-677G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871419 | |||||||
chr18:45871431 | T | C | 5 | a0001c0001t0001g0165 a0011c0022t0020g0045 a0011c0022t0021g0046 others(2): Show |
5 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6050-689A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871431 | |||||||
chr18:45871537 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6050-795A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871537 | |||||||
chr18:45871645 | T | A | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-903A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871645 | |||||||
chr18:45871646 | G | C | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-904C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871646 | |||||||
chr18:45871647 | G | T | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-905C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871647 | |||||||
chr18:45871651 | A | T | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-909T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871651 | |||||||
chr18:45871653 | T | G | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-911A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871653 | |||||||
chr18:45871655 | A | G | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-913T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871655 | |||||||
chr18:45871658 | C | T | 1 | a0002c0002t0008g0243 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-916G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871658 | |||||||
chr18:45871891 | A | AG | 14 | a0002c0002t0002g0245 a0002c0002t0002g0247 a0002c0002t0002g0250 others(11): Show |
14 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.6050-1150_6050-114 others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871891 | |||||||
chr18:45871892 | C | G | 14 | a0002c0002t0002g0245 a0002c0002t0002g0247 a0002c0002t0002g0250 others(11): Show |
14 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.6050-1150G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871892 | |||||||
chr18:45871966 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.6050-1224C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871966 | |||||||
chr18:45872074 | A | AT | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6050-1333dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872074 | |||||||
chr18:45872331 | T | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.6050-1589A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872331 | |||||||
chr18:45872499 | T | A | 1 | a0004c0014t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6050-1757A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872499 | |||||||
chr18:45872502 | G | A | 2 | a0004c0014t0003g0090 a0004c0014t0035g0101 |
2 | HG01123.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.6050-1760C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872502 | |||||||
chr18:45872602 | G | A | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6050-1860C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872602 | |||||||
chr18:45872831 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6050-2089C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872831 | |||||||
chr18:45872971 | C | T | 3 | a0002c0002t0014g0219 a0014c0015t0014g0289 a0014c0015t0019g0290 |
3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.6050-2229G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872971 | |||||||
chr18:45872972 | G | C | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6050-2230C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872972 | |||||||
chr18:45874059 | C | T | 2 | a0002c0002t0029g0227 a0015c0042t0022g0044 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6049+2177G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874059 | |||||||
chr18:45874198 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0126 |
3 | HG00639.hp1 HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6049+2038A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874198 | |||||||
chr18:45874236 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0123 others(3): Show |
6 | HG00280.hp1 HG00741.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049+2000C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874236 | |||||||
chr18:45874350 | A | T | 2 | a0001c0001t0001g0143 a0001c0001t0039g0098 |
2 | NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.6049+1886T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874350 | |||||||
chr18:45874363 | CA | C | 7 | a0002c0002t0002g0238 a0002c0002t0002g0268 a0008c0008t0002g0021 others(4): Show |
7 | HG01358.hp2 HG02071.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.6049+1872delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874363 | |||||||
chr18:45874365 | A | G | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | NA18968.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.6049+1871T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874365 | |||||||
chr18:45874658 | G | A | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6049+1578C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874658 | |||||||
chr18:45874821 | T | C | 15 | a0001c0001t0003g0133 a0001c0001t0005g0099 a0002c0002t0017g0228 others(12): Show |
16 | HG00735.hp1 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.6049+1415A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874821 | |||||||
chr18:45874889 | C | T | 1 | a0003c0003t0016g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.6049+1347G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874889 | |||||||
chr18:45875088 | G | C | 2 | a0013c0026t0005g0024 a0013c0026t0005g0025 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.6049+1148C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875088 | |||||||
chr18:45875221 | G | C | 1 | a0004c0005t0003g0107 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.6049+1015C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875221 | |||||||
chr18:45875264 | C | A | 72 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0032g0115 others(69): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.6049+972G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875264 | |||||||
chr18:45875461 | T | C | 16 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0004g0059 others(13): Show |
16 | HG00609.hp2 HG00621.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.6049+775A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875461 | |||||||
chr18:45875597 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6049+639G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875597 | |||||||
chr18:45875667 | A | C | 1 | a0002c0002t0003g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.6049+569T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875667 | |||||||
chr18:45875764 | A | G | 7 | a0002c0038t0007g0011 a0009c0007t0007g0008 a0009c0007t0007g0012 others(4): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6049+472T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875764 | |||||||
chr18:45875863 | T | A | 3 | a0002c0002t0029g0227 a0015c0042t0022g0044 a0015c0043t0023g0047 |
3 | HG01109.hp1 HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6049+373A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875863 | |||||||
chr18:45875992 | G | C | 6 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0018c0017t0010g0222 others(3): Show |
6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049+244C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875992 | |||||||
chr18:45876035 | C | T | 1 | a0001c0001t0032g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6049+201G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45876035 | |||||||
chr18:45876062 | GA | G | 6 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0018c0017t0010g0222 others(3): Show |
6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049+173delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45876062 | |||||||
chr18:45876110 | C | T | 37 | a0001c0001t0005g0099 a0002c0002t0014g0219 a0002c0002t0017g0228 others(34): Show |
39 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.6049+126G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45876110 | |||||||
chr18:45876546 | A | C | 6 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0018c0017t0010g0222 others(3): Show |
6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5943-204T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876546 | |||||||
chr18:45876588 | T | C | 11 | a0002c0002t0014g0219 a0002c0038t0007g0011 a0009c0007t0007g0008 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.5943-246A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876588 | |||||||
chr18:45876710 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5943-368C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876710 | |||||||
chr18:45876780 | A | C | 8 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(5): Show |
8 | HG01496.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.5943-438T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876780 | |||||||
chr18:45876846 | C | T | 72 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(69): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.5943-504G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876846 | |||||||
chr18:45876874 | C | A | 1 | a0002c0002t0002g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5943-532G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876874 | |||||||
chr18:45877031 | G | A | 1 | a0002c0002t0029g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5943-689C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877031 | |||||||
chr18:45877297 | T | C | 1 | a0001c0001t0004g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5943-955A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877297 | |||||||
chr18:45877355 | G | T | 1 | a0001c0001t0009g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5943-1013C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877355 | |||||||
chr18:45877639 | A | G | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5942+737T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877639 | |||||||
chr18:45877691 | T | C | 76 | a0001c0001t0002g0174 a0001c0001t0002g0187 a0001c0001t0012g0159 others(73): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.5942+685A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877691 | |||||||
chr18:45877702 | G | A | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5942+674C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877702 | |||||||
chr18:45877886 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.5942+490G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877886 | |||||||
chr18:45878505 | G | A | 3 | a0001c0001t0003g0095 a0004c0025t0003g0019 a0004c0025t0003g0111 |
3 | HG01106.hp1 HG02280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.5870-57C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878505 | |||||||
chr18:45878593 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0126 |
3 | HG00639.hp1 HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5870-145A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878593 | |||||||
chr18:45878620 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.5870-172G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878620 | |||||||
chr18:45878720 | C | T | 6 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0018c0017t0010g0222 others(3): Show |
6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5870-272G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878720 | |||||||
chr18:45879306 | C | A | 4 | a0002c0002t0002g0246 a0002c0002t0002g0251 a0002c0002t0008g0051 others(1): Show |
4 | NA18945.hp1 NA18971.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.5668-92G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879306 | |||||||
chr18:45879395 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5668-181A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879395 | |||||||
chr18:45879398 | T | C | 30 | a0001c0001t0005g0099 a0002c0002t0014g0219 a0002c0002t0017g0228 others(27): Show |
32 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.5668-184A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879398 | |||||||
chr18:45879399 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5668-185C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879399 | |||||||
chr18:45879453 | C | T | 1 | a0002c0040t0002g0266 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.5668-239G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879453 | |||||||
chr18:45879454 | G | A | 1 | a0002c0002t0002g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5668-240C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879454 | |||||||
chr18:45879516 | C | G | 14 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(11): Show |
15 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.5668-302G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879516 | |||||||
chr18:45879589 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5668-375C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879589 | |||||||
chr18:45879778 | C | T | 1 | a0022c0031t0001g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5667+297G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879778 | |||||||
chr18:45880025 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5667+50C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45880025 | |||||||
chr18:45880302 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5519-79G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880302 | |||||||
chr18:45880530 | G | C | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5519-307C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880530 | |||||||
chr18:45880786 | T | A | 15 | a0001c0001t0005g0099 a0002c0002t0017g0228 a0004c0005t0005g0104 others(12): Show |
16 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.5519-563A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880786 | |||||||
chr18:45880872 | G | A | 1 | a0010c0010t0001g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.5519-649C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880872 | |||||||
chr18:45880928 | C | T | 2 | a0003c0003t0012g0199 a0003c0003t0012g0200 |
2 | NA18944.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.5519-705G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880928 | |||||||
chr18:45881039 | C | T | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5519-816G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881039 | |||||||
chr18:45881042 | A | T | 12 | a0002c0002t0014g0219 a0009c0007t0007g0008 a0009c0007t0007g0012 others(9): Show |
13 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.5519-819T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881042 | |||||||
chr18:45881162 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5519-939A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881162 | |||||||
chr18:45881186 | T | G | 9 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0005c0048t0003g0018 others(6): Show |
9 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.5519-963A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881186 | |||||||
chr18:45881400 | T | C | 2 | a0002c0002t0004g0054 a0002c0002t0004g0229 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5518+874A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881400 | |||||||
chr18:45881698 | T | C | 2 | a0014c0015t0014g0289 a0014c0015t0019g0290 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5518+576A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881698 | |||||||
chr18:45881855 | C | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5518+419G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881855 | |||||||
chr18:45882048 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5518+226G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45882048 | |||||||
chr18:45882757 | C | T | 1 | a0001c0034t0001g0089 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5305-270G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882757 | |||||||
chr18:45882884 | G | T | 1 | a0006c0012t0006g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5305-397C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882884 | |||||||
chr18:45882921 | A | G | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5305-434T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882921 | |||||||
chr18:45882964 | G | A | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5305-477C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882964 | |||||||
chr18:45883012 | C | CA | 80 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(77): Show |
84 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.5305-526dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883012 | |||||||
chr18:45883012 | C | CAA | 7 | a0002c0002t0001g0292 a0002c0002t0002g0240 a0002c0002t0002g0256 others(4): Show |
7 | HG02818.hp1 HG03471.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.5305-527_5305-526d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883012 | |||||||
chr18:45883012 | C | CAAAAA | 8 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(5): Show |
8 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5305-530_5305-526d others(7): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883012 | |||||||
chr18:45883015 | A | C | 1 | a0001c0001t0043g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5305-528T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883015 | |||||||
chr18:45883031 | A | AG | 9 | a0001c0001t0001g0074 a0001c0001t0001g0097 a0001c0001t0001g0158 others(6): Show |
9 | HG01175.hp2 HG01243.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.5305-545dupC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883031 | |||||||
chr18:45883031 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.5305-544T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883031 | |||||||
chr18:45883069 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.5305-582C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883069 | |||||||
chr18:45883347 | A | G | 1 | a0002c0002t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5305-860T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883347 | |||||||
chr18:45883361 | A | C | 3 | a0002c0002t0004g0054 a0002c0002t0004g0229 a0002c0002t0026g0234 |
3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5305-874T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883361 | |||||||
chr18:45883461 | C | CTT | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.5305-976_5305-975d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883461 | |||||||
chr18:45883461 | CT | C | 14 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.5305-975delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883461 | |||||||
chr18:45883491 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5305-1004G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883491 | |||||||
chr18:45883507 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5305-1020A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883507 | |||||||
chr18:45883614 | G | GT | 59 | a0001c0001t0003g0116 a0002c0002t0001g0292 a0002c0002t0002g0002 others(56): Show |
61 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.5304+1002dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883614 | |||||||
chr18:45883614 | G | GTT | 9 | a0001c0001t0003g0177 a0002c0002t0002g0239 a0002c0038t0007g0011 others(6): Show |
9 | HG02055.hp1 HG02280.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.5304+1001_5304+100 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883614 | |||||||
chr18:45883614 | GT | G | 24 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0005g0003 others(21): Show |
25 | HG00140.hp1 HG00323.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.5304+1002delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883614 | |||||||
chr18:45883619 | T | TTG | 22 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0143 others(19): Show |
22 | HG00735.hp1 HG01109.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.5304+997_5304+998i others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883619 | |||||||
chr18:45883620 | T | TG | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.5304+996_5304+997i others(3): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883620 | |||||||
chr18:45883621 | T | G | 5 | a0004c0005t0033g0048 a0005c0004t0004g0015 a0005c0004t0009g0037 others(2): Show |
5 | HG01361.hp2 HG02071.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5304+996A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883621 | |||||||
chr18:45883622 | T | G | 20 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0005g0003 others(17): Show |
21 | HG00140.hp1 HG01358.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.5304+995A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883622 | |||||||
chr18:45883629 | T | G | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5304+988A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883629 | |||||||
chr18:45883630 | T | G | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5304+987A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883630 | |||||||
chr18:45883631 | T | G | 2 | a0001c0021t0001g0136 a0001c0021t0004g0137 |
2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.5304+986A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883631 | |||||||
chr18:45883635 | T | G | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5304+982A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883635 | |||||||
chr18:45883659 | G | GT | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5304+957dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883659 | |||||||
chr18:45883694 | A | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5304+923T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883694 | |||||||
chr18:45884521 | A | G | 1 | a0003c0003t0003g0282 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.5304+96T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45884521 | |||||||
chr18:45884860 | C | A | 1 | a0003c0003t0003g0186 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5110-49G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45884860 | |||||||
chr18:45884946 | A | C | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5110-135T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45884946 | |||||||
chr18:45885060 | C | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-249G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885060 | |||||||
chr18:45885063 | G | A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0161 others(2): Show |
5 | HG01109.hp2 NA18747.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.5110-252C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885063 | |||||||
chr18:45885359 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-548A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885359 | |||||||
chr18:45885379 | A | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5110-568T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885379 | |||||||
chr18:45885675 | C | T | 3 | a0005c0004t0005g0030 a0005c0004t0005g0034 a0027c0036t0013g0285 |
3 | HG02572.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5110-864G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885675 | |||||||
chr18:45886185 | G | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-1374C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886185 | |||||||
chr18:45886186 | C | G | 1 | a0003c0003t0003g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5110-1375G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886186 | |||||||
chr18:45886343 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5109+1408C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886343 | |||||||
chr18:45886369 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.5109+1382T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886369 | |||||||
chr18:45886520 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.5109+1231A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886520 | |||||||
chr18:45886568 | C | T | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5109+1183G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886568 | |||||||
chr18:45886571 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+1180A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886571 | |||||||
chr18:45886585 | C | T | 77 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(74): Show |
80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.5109+1166G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886585 | |||||||
chr18:45886763 | A | G | 1 | a0001c0001t0009g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5109+988T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886763 | |||||||
chr18:45886805 | C | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+946G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886805 | |||||||
chr18:45886912 | C | T | 1 | a0002c0002t0002g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5109+839G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886912 | |||||||
chr18:45886953 | G | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+798C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886953 | |||||||
chr18:45887170 | C | T | 1 | a0002c0002t0002g0237 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5109+581G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45887170 | |||||||
chr18:45887519 | G | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+232C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45887519 | |||||||
chr18:45888038 | T | C | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4953-131A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888038 | |||||||
chr18:45888108 | T | C | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4953-201A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888108 | |||||||
chr18:45888116 | G | C | 1 | a0002c0002t0008g0065 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4953-209C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888116 | |||||||
chr18:45888182 | C | T | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4953-275G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888182 | |||||||
chr18:45888191 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0161 others(2): Show |
5 | HG01109.hp2 NA18747.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.4953-284G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888191 | |||||||
chr18:45888256 | C | T | 2 | a0002c0002t0002g0248 a0002c0002t0002g0249 |
2 | HG01981.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4953-349G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888256 | |||||||
chr18:45888313 | A | AT | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4953-407dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888313 | |||||||
chr18:45888317 | A | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4953-410T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888317 | |||||||
chr18:45888327 | G | A | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4953-420C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888327 | |||||||
chr18:45888846 | GT | G | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4953-940delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888846 | |||||||
chr18:45888982 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4952+816G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888982 | |||||||
chr18:45889423 | T | C | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4952+375A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889423 | |||||||
chr18:45889482 | G | A | 1 | a0002c0002t0026g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4952+316C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889482 | |||||||
chr18:45889614 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4952+184C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889614 | |||||||
chr18:45889630 | T | G | 1 | a0005c0004t0003g0033 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4952+168A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889630 | |||||||
chr18:45889992 | C | T | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4810-52G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45889992 | |||||||
chr18:45890169 | C | T | 2 | a0001c0021t0001g0136 a0001c0021t0004g0137 |
2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.4810-229G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890169 | |||||||
chr18:45890381 | G | T | 1 | a0001c0001t0009g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4810-441C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890381 | |||||||
chr18:45890580 | T | TA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4810-641dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890580 | |||||||
chr18:45890717 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4810-777A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890717 | |||||||
chr18:45890799 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.4810-859T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890799 | |||||||
chr18:45891047 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4810-1107A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891047 | |||||||
chr18:45891142 | T | C | 2 | a0012c0020t0004g0171 a0012c0020t0004g0216 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.4810-1202A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891142 | |||||||
chr18:45891163 | C | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-1223G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891163 | |||||||
chr18:45891170 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0038 others(41): Show |
47 | HG00609.hp1 HG01109.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.4810-1230C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891170 | |||||||
chr18:45891236 | C | T | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4810-1296G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891236 | |||||||
chr18:45891376 | G | A | 2 | a0005c0004t0005g0030 a0005c0004t0005g0034 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4810-1436C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891376 | |||||||
chr18:45891498 | C | CA | 27 | a0001c0001t0001g0078 a0002c0002t0002g0256 a0002c0002t0004g0284 others(24): Show |
27 | HG00609.hp2 HG00621.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.4810-1559dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891498 | |||||||
chr18:45891498 | CA | C | 18 | a0001c0001t0001g0161 a0002c0002t0001g0068 a0002c0002t0002g0002 others(15): Show |
21 | HG00733.hp1 HG01081.hp2 NA18747.hp2 others(18): Show |
intron_variant | MODIFIER | c.4810-1559delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891498 | |||||||
chr18:45891962 | C | T | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4810-2022G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891962 | |||||||
chr18:45892070 | A | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.4810-2130T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892070 | |||||||
chr18:45892088 | G | A | 2 | a0002c0002t0030g0050 a0002c0002t0031g0049 |
2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4810-2148C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892088 | |||||||
chr18:45892181 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4810-2241C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892181 | |||||||
chr18:45892191 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4810-2251G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892191 | |||||||
chr18:45892209 | C | CA | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-2270dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892209 | |||||||
chr18:45892302 | T | A | 2 | a0001c0001t0004g0057 a0001c0001t0004g0082 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4810-2362A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892302 | |||||||
chr18:45892359 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-2419A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892359 | |||||||
chr18:45892427 | T | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0160 a0001c0001t0002g0187 others(2): Show |
5 | HG04199.hp2 NA18973.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.4810-2487A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892427 | |||||||
chr18:45892548 | T | A | 1 | a0004c0025t0003g0019 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4810-2608A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892548 | |||||||
chr18:45892613 | C | T | 2 | a0007c0006t0003g0211 a0007c0006t0003g0212 |
2 | HG00323.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4810-2673G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892613 | |||||||
chr18:45892670 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.4810-2730G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892670 | |||||||
chr18:45892708 | C | T | 65 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(62): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.4810-2768G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892708 | |||||||
chr18:45892752 | A | G | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4810-2812T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892752 | |||||||
chr18:45892867 | T | C | 1 | a0002c0002t0002g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4810-2927A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892867 | |||||||
chr18:45893024 | T | C | 5 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.4810-3084A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893024 | |||||||
chr18:45893164 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4810-3224A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893164 | |||||||
chr18:45893254 | T | A | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4810-3314A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893254 | |||||||
chr18:45893410 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4810-3470G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893410 | |||||||
chr18:45893458 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.4810-3518T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893458 | |||||||
chr18:45893505 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4810-3565T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893505 | |||||||
chr18:45893551 | T | TA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.4810-3612dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893551 | |||||||
chr18:45893654 | A | G | 4 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4810-3714T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893654 | |||||||
chr18:45893792 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.4810-3852A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893792 | |||||||
chr18:45893909 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4810-3969C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893909 | |||||||
chr18:45894034 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4810-4094C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894034 | |||||||
chr18:45894275 | C | G | 85 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(82): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.4810-4335G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894275 | |||||||
chr18:45894430 | G | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4810-4490C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894430 | |||||||
chr18:45894476 | A | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-4536T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894476 | |||||||
chr18:45894479 | T | A | 2 | a0001c0001t0004g0057 a0002c0009t0002g0275 |
2 | HG04204.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.4810-4539A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894479 | |||||||
chr18:45894502 | C | T | 2 | a0004c0005t0003g0106 a0004c0005t0034g0087 |
2 | HG00741.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.4810-4562G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894502 | |||||||
chr18:45894712 | G | A | 75 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(72): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.4809+4692C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894712 | |||||||
chr18:45894830 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4809+4574A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894830 | |||||||
chr18:45894858 | G | A | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4809+4546C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894858 | |||||||
chr18:45894958 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4809+4446G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894958 | |||||||
chr18:45895023 | G | A | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4809+4381C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895023 | |||||||
chr18:45895067 | G | A | 1 | a0015c0042t0022g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4809+4337C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895067 | |||||||
chr18:45895077 | C | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.4809+4327G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895077 | |||||||
chr18:45895306 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4809+4098C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895306 | |||||||
chr18:45895424 | T | C | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4809+3980A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895424 | |||||||
chr18:45895437 | C | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4809+3967G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895437 | |||||||
chr18:45895444 | GA | G | 86 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(83): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.4809+3959delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895444 | |||||||
chr18:45895587 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+3817A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895587 | |||||||
chr18:45895772 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4809+3632C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895772 | |||||||
chr18:45895842 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4809+3562T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895842 | |||||||
chr18:45896043 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4809+3361T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896043 | |||||||
chr18:45896137 | C | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4809+3267G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896137 | |||||||
chr18:45896145 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4809+3259T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896145 | |||||||
chr18:45896155 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4809+3249A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896155 | |||||||
chr18:45896156 | A | G | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+3248T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896156 | |||||||
chr18:45896178 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4809+3226A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896178 | |||||||
chr18:45896363 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4809+3041C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896363 | |||||||
chr18:45896421 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.4809+2983C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896421 | |||||||
chr18:45896499 | A | G | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+2905T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896499 | |||||||
chr18:45896631 | ACCTCCTG others(12): Show |
A | 1 | a0001c0001t0003g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4809+2754_4809+277 others(23): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896631 | |||||||
chr18:45896706 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4809+2698C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896706 | |||||||
chr18:45896827 | G | A | 1 | a0031c0047t0002g0267 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4809+2577C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896827 | |||||||
chr18:45896836 | C | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4809+2568G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896836 | |||||||
chr18:45896839 | G | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+2565C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896839 | |||||||
chr18:45897063 | A | G | 2 | a0001c0001t0001g0150 a0010c0010t0001g0154 |
2 | NA18968.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.4809+2341T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897063 | |||||||
chr18:45897259 | T | G | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4809+2145A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897259 | |||||||
chr18:45897285 | T | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4809+2119A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897285 | |||||||
chr18:45897428 | G | A | 4 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4809+1976C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897428 | |||||||
chr18:45897431 | T | C | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4809+1973A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897431 | |||||||
chr18:45897442 | T | TA | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4809+1961_4809+196 others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897442 | |||||||
chr18:45897447 | T | C | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4809+1957A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897447 | |||||||
chr18:45897475 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4809+1929A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897475 | |||||||
chr18:45897497 | T | G | 2 | a0014c0015t0014g0289 a0014c0015t0019g0290 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4809+1907A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897497 | |||||||
chr18:45897513 | C | T | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4809+1891G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897513 | |||||||
chr18:45897640 | G | A | 2 | a0002c0002t0002g0259 a0002c0002t0002g0260 |
2 | NA18968.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4809+1764C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897640 | |||||||
chr18:45897712 | T | C | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4809+1692A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897712 | |||||||
chr18:45897793 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4809+1611T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897793 | |||||||
chr18:45898138 | T | C | 2 | a0005c0004t0004g0015 a0005c0004t0009g0037 |
2 | HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4809+1266A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898138 | |||||||
chr18:45898209 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+1195A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898209 | |||||||
chr18:45898246 | C | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4809+1158G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898246 | |||||||
chr18:45898277 | G | A | 3 | a0003c0003t0003g0194 a0003c0003t0003g0196 a0003c0003t0042g0195 |
3 | NA18966.hp2 NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.4809+1127C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898277 | |||||||
chr18:45898603 | A | G | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4809+801T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898603 | |||||||
chr18:45898823 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4809+581G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898823 | |||||||
chr18:45898848 | C | T | 2 | a0014c0015t0014g0289 a0014c0015t0019g0290 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4809+556G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898848 | |||||||
chr18:45898865 | G | A | 1 | a0005c0004t0005g0003 | 2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4809+539C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898865 | |||||||
chr18:45898892 | C | A | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4809+512G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898892 | |||||||
chr18:45898977 | T | A | 1 | a0002c0009t0002g0279 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4809+427A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898977 | |||||||
chr18:45899018 | G | A | 87 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(84): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.4809+386C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45899018 | |||||||
chr18:45899099 | T | C | 75 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(72): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.4809+305A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45899099 | |||||||
chr18:45899339 | T | C | 2 | a0001c0001t0004g0072 a0002c0038t0007g0011 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4809+65A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45899339 | |||||||
chr18:45899798 | T | C | 1 | a0002c0002t0002g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4647-232A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899798 | |||||||
chr18:45899855 | G | C | 1 | a0003c0003t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4647-289C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899855 | |||||||
chr18:45899903 | T | C | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4647-337A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899903 | |||||||
chr18:45899975 | C | G | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4647-409G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899975 | |||||||
chr18:45900102 | T | C | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4647-536A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900102 | |||||||
chr18:45900103 | G | A | 1 | a0002c0002t0030g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4647-537C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900103 | |||||||
chr18:45900105 | T | C | 1 | a0008c0008t0001g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4647-539A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900105 | |||||||
chr18:45900130 | T | C | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4647-564A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900130 | |||||||
chr18:45900404 | C | CA | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.4646+591dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900404 | |||||||
chr18:45900404 | C | CAA | 8 | a0001c0001t0001g0153 a0001c0001t0001g0169 a0002c0002t0002g0268 others(5): Show |
8 | HG01192.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.4646+590_4646+591d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900404 | |||||||
chr18:45900495 | C | T | 78 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(75): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.4646+501G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900495 | |||||||
chr18:45900564 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4646+432C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900564 | |||||||
chr18:45900590 | C | T | 5 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4646+406G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900590 | |||||||
chr18:45900806 | C | A | 91 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(88): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.4646+190G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900806 | |||||||
chr18:45900818 | G | A | 1 | a0019c0016t0010g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4646+178C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900818 | |||||||
chr18:45900856 | A | C | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4646+140T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900856 | |||||||
chr18:45900961 | A | G | 91 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(88): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.4646+35T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900961 | |||||||
chr18:45901268 | T | G | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4475-101A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901268 | |||||||
chr18:45901290 | G | C | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4475-123C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901290 | |||||||
chr18:45901405 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4475-238G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901405 | |||||||
chr18:45901625 | G | A | 1 | a0002c0002t0008g0242 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4475-458C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901625 | |||||||
chr18:45901649 | T | G | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4475-482A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901649 | |||||||
chr18:45901765 | C | CCA | 13 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(10): Show |
16 | HG00609.hp2 HG00741.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.4475-600_4475-599d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | |||||||
chr18:45901765 | C | CCACA | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.4475-602_4475-599d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | |||||||
chr18:45901765 | C | CCACACA | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4475-604_4475-599d others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | |||||||
chr18:45901765 | C | CCACACAC others(1): Show |
3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4475-606_4475-599d others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | |||||||
chr18:45901765 | CCA | C | 5 | a0002c0002t0002g0262 a0002c0002t0014g0219 a0006c0012t0006g0220 others(2): Show |
5 | HG01261.hp2 HG01891.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.4475-600_4475-599d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | |||||||
chr18:45901765 | CCACA | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0152 others(6): Show |
13 | HG02083.hp1 HG02523.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.4475-602_4475-599d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | |||||||
chr18:45901790 | C | CAT | 5 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0160 others(2): Show |
6 | HG00438.hp2 HG00639.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.4475-624_4475-623i others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901790 | |||||||
chr18:45901790 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0038 others(107): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.4475-623G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901790 | |||||||
chr18:45901803 | G | C | 1 | a0001c0001t0032g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4475-636C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901803 | |||||||
chr18:45901833 | T | G | 1 | a0001c0001t0005g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4475-666A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901833 | |||||||
chr18:45901920 | T | C | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4475-753A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901920 | |||||||
chr18:45901959 | T | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4475-792A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901959 | |||||||
chr18:45902128 | T | C | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4475-961A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902128 | |||||||
chr18:45902138 | A | G | 1 | a0005c0004t0003g0033 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4475-971T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902138 | |||||||
chr18:45902280 | C | T | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4475-1113G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902280 | |||||||
chr18:45902295 | T | G | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4475-1128A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902295 | |||||||
chr18:45902681 | CTCTTA | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0176 a0001c0030t0001g0139 |
3 | NA18948.hp2 NA18967.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.4474+1287_4474+129 others(9): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902681 | |||||||
chr18:45902743 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0094 others(36): Show |
42 | HG00609.hp1 HG01109.hp2 HG02074.hp2 others(39): Show |
intron_variant | MODIFIER | c.4474+1230C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902743 | |||||||
chr18:45903021 | G | A | 5 | a0002c0002t0002g0055 a0002c0002t0002g0238 a0002c0002t0002g0268 others(2): Show |
5 | NA18940.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.4474+952C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903021 | |||||||
chr18:45903059 | T | A | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4474+914A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903059 | |||||||
chr18:45903078 | G | A | 5 | a0001c0001t0001g0129 a0009c0007t0007g0008 a0009c0007t0007g0013 others(2): Show |
6 | HG02109.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4474+895C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903078 | |||||||
chr18:45903113 | AT | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4474+859delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903113 | |||||||
chr18:45903184 | C | T | 1 | a0004c0014t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4474+789G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903184 | |||||||
chr18:45903186 | T | C | 1 | a0001c0001t0043g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4474+787A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903186 | |||||||
chr18:45903213 | C | A | 18 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0122 others(15): Show |
18 | HG00609.hp1 HG02074.hp2 HG04199.hp2 others(15): Show |
intron_variant | MODIFIER | c.4474+760G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903213 | |||||||
chr18:45903360 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4474+613C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903360 | |||||||
chr18:45903414 | G | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4474+559C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903414 | |||||||
chr18:45903487 | T | G | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4474+486A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903487 | |||||||
chr18:45903514 | G | A | 1 | a0002c0002t0002g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4474+459C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903514 | |||||||
chr18:45904160 | T | G | 2 | a0001c0001t0005g0099 a0001c0001t0032g0115 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4330-43A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904160 | |||||||
chr18:45904326 | T | C | 10 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(7): Show |
10 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.4330-209A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904326 | |||||||
chr18:45904376 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4330-259G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904376 | |||||||
chr18:45904552 | G | A | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4330-435C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904552 | |||||||
chr18:45904630 | G | A | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4330-513C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904630 | |||||||
chr18:45904701 | C | A | 4 | a0001c0001t0004g0215 a0001c0001t0009g0217 a0012c0020t0004g0171 others(1): Show |
4 | HG00438.hp1 HG00621.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.4330-584G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904701 | |||||||
chr18:45904737 | TA | T | 91 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(88): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.4330-621delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904737 | |||||||
chr18:45905054 | A | G | 80 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(77): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.4330-937T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905054 | |||||||
chr18:45905184 | T | C | 1 | a0015c0043t0023g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4330-1067A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905184 | |||||||
chr18:45905384 | A | G | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4330-1267T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905384 | |||||||
chr18:45905558 | C | A | 2 | a0014c0015t0014g0289 a0014c0015t0019g0290 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4330-1441G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905558 | |||||||
chr18:45905745 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4330-1628T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905745 | |||||||
chr18:45905975 | C | T | 1 | a0026c0041t0007g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4330-1858G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905975 | |||||||
chr18:45905996 | G | C | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4330-1879C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905996 | |||||||
chr18:45906009 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | NA18964.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.4330-1892T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906009 | |||||||
chr18:45906168 | C | A | 1 | a0003c0003t0003g0186 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4329+1790G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906168 | |||||||
chr18:45906173 | C | T | 5 | a0005c0004t0005g0003 a0005c0004t0005g0026 a0005c0004t0005g0027 others(2): Show |
6 | HG02257.hp1 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4329+1785G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906173 | |||||||
chr18:45906319 | A | G | 1 | a0002c0009t0002g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4329+1639T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906319 | |||||||
chr18:45906394 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0138 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.4329+1564G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906394 | |||||||
chr18:45906655 | AT | A | 16 | a0001c0001t0001g0102 a0001c0001t0001g0149 a0001c0001t0001g0157 others(13): Show |
16 | HG01884.hp1 HG01981.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.4329+1302delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906655 | |||||||
chr18:45906670 | T | A | 1 | a0002c0002t0002g0238 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4329+1288A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906670 | |||||||
chr18:45906679 | G | GTC | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4329+1277_4329+127 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906679 | |||||||
chr18:45906815 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.4329+1143G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906815 | |||||||
chr18:45906888 | T | G | 1 | a0008c0008t0002g0022 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4329+1070A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906888 | |||||||
chr18:45906937 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4329+1021A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906937 | |||||||
chr18:45907281 | A | G | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4329+677T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907281 | |||||||
chr18:45907350 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0081 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.4329+608T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907350 | |||||||
chr18:45907406 | G | T | 1 | a0004c0005t0016g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4329+552C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907406 | |||||||
chr18:45907408 | C | A | 1 | a0004c0005t0016g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4329+550G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907408 | |||||||
chr18:45907453 | G | A | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4329+505C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907453 | |||||||
chr18:45907514 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4329+444G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907514 | |||||||
chr18:45907548 | C | G | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4329+410G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907548 | |||||||
chr18:45907611 | T | C | 75 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(72): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.4329+347A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907611 | |||||||
chr18:45907658 | A | G | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4329+300T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907658 | |||||||
chr18:45907704 | T | C | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4329+254A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907704 | |||||||
chr18:45907761 | C | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4329+197G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907761 | |||||||
chr18:45907920 | TA | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
124 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.4329+37delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907920 | |||||||
chr18:45907920 | TAA | T | 6 | a0001c0001t0001g0069 a0001c0001t0001g0130 a0001c0001t0001g0135 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4329+36_4329+37del others(2): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907920 | |||||||
chr18:45908107 | G | A | 4 | a0001c0001t0011g0151 a0001c0001t0011g0181 a0001c0001t0011g0182 others(1): Show |
4 | HG01109.hp2 HG01261.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.4206-26C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45908107 | |||||||
chr18:45908874 | G | A | 90 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(87): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4206-793C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45908874 | |||||||
chr18:45908948 | C | CA | 12 | a0002c0002t0002g0283 a0005c0004t0015g0017 a0005c0048t0003g0018 others(9): Show |
12 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.4206-868dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45908948 | |||||||
chr18:45909138 | T | C | 1 | a0002c0002t0031g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4206-1057A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909138 | |||||||
chr18:45909301 | A | G | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4205+1220T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909301 | |||||||
chr18:45909329 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4205+1192G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909329 | |||||||
chr18:45909389 | T | C | 1 | a0015c0042t0022g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4205+1132A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909389 | |||||||
chr18:45909445 | G | C | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4205+1076C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909445 | |||||||
chr18:45909451 | G | A | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4205+1070C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909451 | |||||||
chr18:45909682 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0167 |
2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4205+839A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909682 | |||||||
chr18:45909692 | A | C | 1 | a0001c0001t0040g0141 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4205+829T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909692 | |||||||
chr18:45909742 | G | A | 1 | a0002c0002t0025g0067 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4205+779C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909742 | |||||||
chr18:45909752 | T | C | 4 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4205+769A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909752 | |||||||
chr18:45909922 | T | C | 1 | a0012c0020t0004g0216 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4205+599A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909922 | |||||||
chr18:45910135 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0167 others(2): Show |
5 | NA18948.hp2 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.4205+386C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45910135 | |||||||
chr18:45910189 | A | G | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4205+332T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45910189 | |||||||
chr18:45910447 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4205+74A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45910447 | |||||||
chr18:45910762 | G | C | 1 | a0002c0002t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3984-20C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45910762 | |||||||
chr18:45910983 | C | T | 1 | a0020c0023t0002g0257 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3984-241G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45910983 | |||||||
chr18:45911073 | ATC | A | 2 | a0003c0013t0001g0006 a0005c0004t0015g0017 |
3 | HG02922.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3984-333_3984-332d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911073 | |||||||
chr18:45911075 | C | A | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3984-333G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911075 | |||||||
chr18:45911076 | T | C | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3984-334A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911076 | |||||||
chr18:45911078 | T | C | 3 | a0003c0013t0001g0006 a0005c0004t0015g0017 a0005c0048t0003g0018 |
4 | HG02922.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3984-336A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | |||||||
chr18:45911078 | T | TACACACA others(3): Show |
2 | a0009c0007t0007g0014 a0009c0007t0007g0016 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3984-346_3984-337d others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | |||||||
chr18:45911078 | T | TCTATAC | 19 | a0005c0004t0001g0031 a0005c0004t0004g0015 a0005c0004t0005g0003 others(16): Show |
20 | HG01358.hp2 HG01361.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3984-337_3984-336i others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | |||||||
chr18:45911078 | TAC | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.3984-338_3984-337d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | |||||||
chr18:45911078 | TACAC | T | 3 | a0001c0001t0001g0126 a0001c0001t0005g0099 a0002c0002t0002g0265 |
3 | HG00639.hp1 HG02055.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.3984-340_3984-337d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | |||||||
chr18:45911080 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3984-338G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911080 | |||||||
chr18:45911104 | C | T | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3984-362G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911104 | |||||||
chr18:45911106 | C | CAT | 5 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG01243.hp2 HG02071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3984-365_3984-364i others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911106 | |||||||
chr18:45911106 | C | T | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3984-364G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911106 | |||||||
chr18:45911108 | C | T | 37 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0114 others(34): Show |
38 | HG01243.hp2 HG01358.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.3984-366G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911108 | |||||||
chr18:45911110 | C | CACACACA others(1): Show |
4 | a0002c0002t0017g0228 a0006c0012t0006g0221 a0006c0012t0006g0226 others(1): Show |
4 | HG02647.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3984-369_3984-368i others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | |||||||
chr18:45911110 | C | CACACATA others(1): Show |
4 | a0002c0002t0014g0219 a0002c0002t0029g0227 a0006c0012t0006g0220 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3984-369_3984-368i others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | |||||||
chr18:45911110 | C | CAT | 33 | a0002c0038t0007g0011 a0003c0003t0001g0203 a0003c0003t0002g0286 others(30): Show |
33 | HG00323.hp1 HG00733.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.3984-370_3984-369d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | |||||||
chr18:45911110 | C | CATAT | 23 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 others(20): Show |
23 | HG01928.hp2 HG02622.hp1 HG02723.hp1 others(20): Show |
intron_variant | MODIFIER | c.3984-372_3984-369d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | |||||||
chr18:45911110 | C | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0061 others(107): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.3984-368G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | |||||||
chr18:45911129 | A | AT | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3984-388dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911129 | |||||||
chr18:45911153 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3984-411C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911153 | |||||||
chr18:45911289 | G | GT | 26 | a0001c0001t0004g0059 a0002c0002t0002g0230 a0003c0003t0003g0190 others(23): Show |
27 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.3984-548dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911289 | |||||||
chr18:45911363 | G | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3984-621C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911363 | |||||||
chr18:45911388 | C | T | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3984-646G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911388 | |||||||
chr18:45911462 | A | AT | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3984-721dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911462 | |||||||
chr18:45911464 | T | A | 1 | a0008c0008t0002g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3984-722A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911464 | |||||||
chr18:45911509 | G | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3984-767C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911509 | |||||||
chr18:45911544 | G | A | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3983+746C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911544 | |||||||
chr18:45911572 | G | A | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3983+718C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911572 | |||||||
chr18:45911626 | A | G | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3983+664T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911626 | |||||||
chr18:45911924 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3983+366C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911924 | |||||||
chr18:45911926 | G | A | 1 | a0006c0012t0006g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3983+364C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911926 | |||||||
chr18:45912099 | C | T | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG01943.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3983+191G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45912099 | |||||||
chr18:45912156 | CAGAG | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.3983+130_3983+133d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45912156 | |||||||
chr18:45912520 | T | C | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3817-64A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912520 | |||||||
chr18:45912673 | A | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3817-217T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912673 | |||||||
chr18:45912787 | A | G | 1 | a0002c0002t0008g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3817-331T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912787 | |||||||
chr18:45912895 | C | A | 2 | a0002c0002t0002g0256 a0002c0002t0002g0263 |
2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3817-439G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912895 | |||||||
chr18:45913065 | C | T | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.3817-609G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913065 | |||||||
chr18:45913090 | CA | C | 102 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(99): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.3816+615delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913090 | |||||||
chr18:45913194 | C | T | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3816+512G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913194 | |||||||
chr18:45913265 | C | T | 1 | a0002c0002t0003g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3816+441G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913265 | |||||||
chr18:45913363 | G | A | 2 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3816+343C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913363 | |||||||
chr18:45913622 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3816+84T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913622 | |||||||
chr18:45913624 | A | G | 15 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0147 others(12): Show |
15 | HG01109.hp2 HG02165.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.3816+82T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913624 | |||||||
chr18:45913912 | C | A | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3694-84G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45913912 | |||||||
chr18:45914138 | C | T | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3694-310G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914138 | |||||||
chr18:45914149 | A | G | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3694-321T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914149 | |||||||
chr18:45914220 | G | A | 2 | a0001c0001t0001g0150 a0010c0010t0001g0154 |
2 | NA18968.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.3694-392C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914220 | |||||||
chr18:45914376 | C | T | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3694-548G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914376 | |||||||
chr18:45914451 | G | T | 78 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(75): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.3694-623C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914451 | |||||||
chr18:45914513 | C | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3694-685G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914513 | |||||||
chr18:45914765 | C | T | 7 | a0002c0002t0002g0230 a0002c0002t0002g0259 a0002c0002t0002g0260 others(4): Show |
7 | HG00733.hp1 NA18968.hp1 NA19006.hp2 others(4): Show |
intron_variant | MODIFIER | c.3693+746G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914765 | |||||||
chr18:45914776 | G | A | 2 | a0001c0001t0005g0099 a0001c0001t0032g0115 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3693+735C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914776 | |||||||
chr18:45914875 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3693+636C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914875 | |||||||
chr18:45914876 | G | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3693+635C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914876 | |||||||
chr18:45914905 | A | G | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3693+606T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914905 | |||||||
chr18:45914970 | TA | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3693+540delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914970 | |||||||
chr18:45914970 | TAA | T | 13 | a0001c0001t0001g0102 a0001c0001t0001g0147 a0001c0001t0004g0073 others(10): Show |
13 | HG00323.hp2 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.3693+539_3693+540d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914970 | |||||||
chr18:45915004 | C | T | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.3693+507G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915004 | |||||||
chr18:45915045 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3693+466C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915045 | |||||||
chr18:45915072 | A | G | 90 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(87): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3693+439T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915072 | |||||||
chr18:45915096 | T | C | 1 | a0001c0001t0011g0151 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3693+415A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915096 | |||||||
chr18:45915111 | T | C | 12 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.3693+400A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915111 | |||||||
chr18:45915147 | G | A | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3693+364C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915147 | |||||||
chr18:45915255 | G | A | 1 | a0001c0001t0005g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3693+256C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915255 | |||||||
chr18:45915299 | T | A | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.3693+212A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915299 | |||||||
chr18:45915392 | T | C | 1 | a0001c0001t0039g0098 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3693+119A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915392 | |||||||
chr18:45915425 | T | G | 1 | a0012c0020t0004g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3693+86A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915425 | |||||||
chr18:45915451 | G | T | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3693+60C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915451 | |||||||
chr18:45915802 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3583-181G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/43 | chr18 | 45915802 | |||||||
chr18:45915997 | C | G | 1 | a0003c0003t0003g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3582+12G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/43 | chr18 | 45915997 | |||||||
chr18:45916226 | G | A | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3385-20C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/43 | chr18 | 45916226 | |||||||
chr18:45916415 | T | C | 1 | a0003c0003t0003g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3384+23A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/43 | chr18 | 45916415 | |||||||
chr18:45916728 | A | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3240-146T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45916728 | |||||||
chr18:45916798 | G | A | 26 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0086 others(23): Show |
26 | HG00099.hp1 HG01081.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.3240-216C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45916798 | |||||||
chr18:45916865 | C | T | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3240-283G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45916865 | |||||||
chr18:45917022 | G | A | 15 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0053 others(12): Show |
18 | HG00733.hp1 NA18951.hp2 NA18966.hp1 others(15): Show |
intron_variant | MODIFIER | c.3240-440C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917022 | |||||||
chr18:45917102 | G | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3240-520C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917102 | |||||||
chr18:45917151 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3239+528T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917151 | |||||||
chr18:45917188 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3239+491G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917188 | |||||||
chr18:45917225 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3239+454A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917225 | |||||||
chr18:45917272 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3239+407A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917272 | |||||||
chr18:45917541 | G | A | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3239+138C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917541 | |||||||
chr18:45917643 | T | C | 1 | a0005c0004t0001g0031 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3239+36A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917643 | |||||||
chr18:45917972 | G | A | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3099-153C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45917972 | |||||||
chr18:45918091 | G | A | 5 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3099-272C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918091 | |||||||
chr18:45918130 | C | T | 75 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(72): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.3099-311G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918130 | |||||||
chr18:45918329 | G | A | 1 | a0005c0004t0009g0037 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3099-510C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918329 | |||||||
chr18:45918403 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3099-584G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918403 | |||||||
chr18:45918561 | C | T | 104 | a0001c0001t0001g0123 a0002c0002t0001g0066 a0002c0002t0001g0068 others(101): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.3099-742G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918561 | |||||||
chr18:45918564 | A | T | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3099-745T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918564 | |||||||
chr18:45919042 | C | T | 1 | a0002c0002t0004g0284 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3099-1223G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919042 | |||||||
chr18:45919177 | C | T | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.3099-1358G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919177 | |||||||
chr18:45919336 | A | C | 1 | a0009c0007t0007g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3099-1517T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919336 | |||||||
chr18:45919431 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3099-1612C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919431 | |||||||
chr18:45919439 | A | G | 1 | a0002c0002t0008g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3099-1620T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919439 | |||||||
chr18:45919459 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3099-1640A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919459 | |||||||
chr18:45919514 | G | GT | 37 | a0001c0001t0004g0082 a0001c0001t0004g0119 a0001c0021t0001g0136 others(34): Show |
38 | HG00140.hp1 HG00621.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.3099-1696dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919514 | |||||||
chr18:45919573 | C | T | 3 | a0002c0002t0004g0054 a0002c0002t0004g0229 a0002c0002t0026g0234 |
3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3099-1754G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919573 | |||||||
chr18:45919576 | A | C | 3 | a0002c0002t0004g0054 a0002c0002t0004g0229 a0002c0002t0026g0234 |
3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3099-1757T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919576 | |||||||
chr18:45919584 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3099-1765G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919584 | |||||||
chr18:45919597 | C | T | 70 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(67): Show |
73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.3099-1778G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919597 | |||||||
chr18:45919653 | C | T | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3099-1834G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919653 | |||||||
chr18:45919705 | G | T | 4 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3099-1886C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919705 | |||||||
chr18:45920081 | G | A | 5 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3098+2260C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920081 | |||||||
chr18:45920089 | G | A | 2 | a0012c0020t0004g0171 a0012c0020t0004g0216 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.3098+2252C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920089 | |||||||
chr18:45920102 | A | G | 3 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 |
3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3098+2239T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920102 | |||||||
chr18:45920317 | T | G | 2 | a0001c0001t0001g0152 a0001c0001t0009g0146 |
2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3098+2024A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920317 | |||||||
chr18:45920442 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3098+1899C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920442 | |||||||
chr18:45920575 | G | A | 1 | a0004c0014t0003g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3098+1766C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920575 | |||||||
chr18:45921333 | A | T | 2 | a0014c0015t0014g0289 a0014c0015t0019g0290 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3098+1008T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921333 | |||||||
chr18:45921503 | T | C | 2 | a0003c0003t0003g0207 a0003c0003t0003g0208 |
2 | NA18957.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3098+838A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921503 | |||||||
chr18:45921779 | A | C | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3098+562T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921779 | |||||||
chr18:45921801 | A | G | 124 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(121): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.3098+540T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921801 | |||||||
chr18:45921811 | A | G | 103 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(100): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.3098+530T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921811 | |||||||
chr18:45921939 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG02083.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3098+402A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921939 | |||||||
chr18:45921963 | T | TGAA | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3098+377_3098+378i others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921963 | |||||||
chr18:45921963 | TA | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0102 others(8): Show |
11 | HG02735.hp2 HG03834.hp2 HG06807.hp1 others(8): Show |
intron_variant | MODIFIER | c.3098+377delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921963 | |||||||
chr18:45922071 | C | T | 1 | a0003c0013t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3098+270G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45922071 | |||||||
chr18:45922090 | A | G | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3098+251T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45922090 | |||||||
chr18:45922224 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.3098+117C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45922224 | |||||||
chr18:45922697 | A | G | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2839-97T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922697 | |||||||
chr18:45922762 | T | C | 127 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(124): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.2839-162A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922762 | |||||||
chr18:45922901 | T | C | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2839-301A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922901 | |||||||
chr18:45922978 | T | G | 1 | a0002c0002t0027g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2838+290A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922978 | |||||||
chr18:45923074 | T | C | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2838+194A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45923074 | |||||||
chr18:45923190 | A | G | 1 | a0002c0002t0002g0244 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2838+78T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45923190 | |||||||
chr18:45923697 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2719-310C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923697 | |||||||
chr18:45923769 | C | T | 3 | a0003c0003t0003g0194 a0003c0003t0003g0196 a0003c0003t0042g0195 |
3 | NA18966.hp2 NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2719-382G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923769 | |||||||
chr18:45923771 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2719-384C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923771 | |||||||
chr18:45923891 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2719-504C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923891 | |||||||
chr18:45924026 | CA | C | 12 | a0001c0001t0001g0114 a0001c0001t0001g0158 a0002c0009t0002g0276 others(9): Show |
12 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2719-640delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924026 | |||||||
chr18:45924041 | A | G | 9 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2719-654T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924041 | |||||||
chr18:45924108 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2719-721A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924108 | |||||||
chr18:45924173 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2719-786T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924173 | |||||||
chr18:45924274 | C | T | 5 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2719-887G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924274 | |||||||
chr18:45924392 | T | C | 1 | a0001c0001t0004g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2719-1005A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924392 | |||||||
chr18:45924393 | A | T | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2719-1006T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924393 | |||||||
chr18:45924456 | T | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0118 others(19): Show |
23 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.2719-1069A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924456 | |||||||
chr18:45924812 | C | T | 70 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(67): Show |
73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2718+926G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924812 | |||||||
chr18:45924813 | G | A | 1 | a0001c0001t0005g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2718+925C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924813 | |||||||
chr18:45924942 | A | G | 1 | a0005c0004t0015g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2718+796T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924942 | |||||||
chr18:45925011 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2718+727A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925011 | |||||||
chr18:45925231 | G | A | 70 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0002 others(67): Show |
73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2718+507C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925231 | |||||||
chr18:45925293 | A | G | 100 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0001g0292 others(97): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2718+445T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925293 | |||||||
chr18:45925508 | G | A | 1 | a0006c0011t0006g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2718+230C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925508 | |||||||
chr18:45925592 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2718+146G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925592 | |||||||
chr18:45926141 | A | G | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2554-239T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926141 | |||||||
chr18:45926331 | G | C | 2 | a0006c0012t0006g0271 a0015c0043t0023g0047 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2554-429C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926331 | |||||||
chr18:45926464 | A | C | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2554-562T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926464 | |||||||
chr18:45926514 | A | T | 5 | a0002c0002t0002g0055 a0002c0002t0002g0238 a0002c0002t0002g0268 others(2): Show |
5 | NA18940.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2554-612T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926514 | |||||||
chr18:45926727 | C | G | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2554-825G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926727 | |||||||
chr18:45926816 | G | GA | 288 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.2554-915dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926816 | |||||||
chr18:45926962 | G | A | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2554-1060C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926962 | |||||||
chr18:45927035 | C | CT | 62 | a0001c0001t0001g0103 a0001c0001t0040g0141 a0001c0021t0001g0136 others(59): Show |
65 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.2554-1134dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927035 | |||||||
chr18:45927035 | C | CTT | 6 | a0002c0002t0002g0283 a0002c0009t0002g0275 a0018c0017t0010g0222 others(3): Show |
6 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2554-1135_2554-113 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927035 | |||||||
chr18:45927094 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2554-1192C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927094 | |||||||
chr18:45927146 | C | T | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2554-1244G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927146 | |||||||
chr18:45927193 | C | T | 6 | a0002c0002t0002g0052 a0002c0002t0002g0237 a0002c0002t0002g0269 others(3): Show |
6 | NA18747.hp1 NA18941.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2554-1291G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927193 | |||||||
chr18:45927203 | G | GT | 7 | a0001c0001t0001g0144 a0001c0001t0004g0057 a0001c0001t0004g0070 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2554-1302dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927203 | |||||||
chr18:45927214 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2554-1312G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927214 | |||||||
chr18:45927241 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2554-1339C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927241 | |||||||
chr18:45927257 | T | C | 1 | a0002c0002t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2554-1355A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927257 | |||||||
chr18:45927291 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2554-1389C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927291 | |||||||
chr18:45927299 | G | A | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2554-1397C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927299 | |||||||
chr18:45927405 | T | C | 35 | a0003c0003t0001g0185 a0003c0003t0001g0192 a0003c0003t0001g0193 others(32): Show |
36 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.2553+1464A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927405 | |||||||
chr18:45927507 | C | T | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2553+1362G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927507 | |||||||
chr18:45927513 | C | T | 116 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.2553+1356G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927513 | |||||||
chr18:45927591 | T | TACAC | 3 | a0018c0017t0010g0222 a0019c0016t0010g0224 a0019c0016t0010g0225 |
3 | HG02818.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2553+1277_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | |||||||
chr18:45927591 | TATAC | T | 9 | a0002c0002t0029g0227 a0002c0038t0007g0011 a0009c0007t0007g0008 others(6): Show |
10 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2553+1274_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | |||||||
chr18:45927591 | TATACAC | T | 4 | a0002c0002t0017g0228 a0002c0002t0030g0050 a0002c0009t0002g0276 others(1): Show |
4 | HG02647.hp2 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2553+1272_2553+127 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | |||||||
chr18:45927591 | TATACACA others(1): Show |
T | 57 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(54): Show |
60 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2553+1270_2553+127 others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | |||||||
chr18:45927591 | TATACACA others(5): Show |
T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2553+1266_2553+127 others(16): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | |||||||
chr18:45927592 | A | G | 6 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2553+1277T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927592 | |||||||
chr18:45927593 | T | C | 10 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2553+1276A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | T | TAC | 40 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0094 others(37): Show |
41 | HG00323.hp1 HG00323.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.2553+1274_2553+127 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | T | TACAC | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0061 others(74): Show |
80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2553+1272_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | T | TACACAC | 41 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0081 others(38): Show |
42 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2553+1270_2553+127 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | T | TACACACA others(1): Show |
10 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0167 others(7): Show |
10 | HG00609.hp1 HG01346.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2553+1268_2553+127 others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | T | TATAC | 19 | a0005c0004t0001g0031 a0005c0004t0004g0015 a0005c0004t0005g0003 others(16): Show |
20 | HG01358.hp2 HG01361.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2553+1275_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | T | TATACAC | 3 | a0005c0004t0003g0033 a0005c0004t0015g0017 a0008c0008t0002g0023 |
3 | HG00140.hp1 HG02071.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2553+1275_2553+127 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927593 | TACACACA others(5): Show |
T | 1 | a0030c0035t0001g0134 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2553+1264_2553+127 others(16): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | |||||||
chr18:45927594 | A | G | 1 | a0009c0007t0007g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2553+1275T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927594 | |||||||
chr18:45927596 | A | G | 8 | a0002c0002t0029g0227 a0009c0007t0007g0008 a0009c0007t0007g0013 others(5): Show |
9 | HG01109.hp1 HG01496.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2553+1273T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927596 | |||||||
chr18:45927598 | A | G | 4 | a0002c0002t0017g0228 a0002c0002t0030g0050 a0002c0009t0002g0276 others(1): Show |
4 | HG02647.hp2 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2553+1271T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927598 | |||||||
chr18:45927600 | A | G | 57 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(54): Show |
60 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2553+1269T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927600 | |||||||
chr18:45927604 | A | G | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2553+1265T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927604 | |||||||
chr18:45927613 | C | CAT | 5 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+1255_2553+125 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927613 | |||||||
chr18:45927871 | T | G | 89 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(86): Show |
93 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.2553+998A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927871 | |||||||
chr18:45927935 | T | C | 2 | a0001c0001t0001g0161 a0023c0049t0001g0179 |
2 | HG01109.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2553+934A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927935 | |||||||
chr18:45927959 | C | T | 1 | a0001c0001t0004g0071 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2553+910G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927959 | |||||||
chr18:45927962 | G | C | 1 | a0002c0002t0003g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2553+907C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927962 | |||||||
chr18:45928053 | G | T | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2553+816C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928053 | |||||||
chr18:45928189 | G | C | 5 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+680C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928189 | |||||||
chr18:45928213 | C | CA | 89 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(86): Show |
93 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.2553+655dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928213 | |||||||
chr18:45928312 | A | G | 2 | a0005c0004t0005g0030 a0005c0004t0005g0034 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2553+557T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928312 | |||||||
chr18:45928632 | G | A | 5 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+237C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928632 | |||||||
chr18:45928641 | A | G | 81 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(78): Show |
85 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.2553+228T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928641 | |||||||
chr18:45928822 | A | C | 5 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+47T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928822 | |||||||
chr18:45928833 | T | TA | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2553+35_2553+36ins others(1): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928833 | |||||||
chr18:45928834 | G | A | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2553+35C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928834 | |||||||
chr18:45929079 | A | G | 84 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(81): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.2413-70T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929079 | |||||||
chr18:45929178 | G | A | 1 | a0001c0034t0001g0089 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2413-169C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929178 | |||||||
chr18:45929273 | C | T | 6 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2413-264G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929273 | |||||||
chr18:45929434 | T | C | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2413-425A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929434 | |||||||
chr18:45929486 | A | G | 1 | a0003c0003t0003g0282 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2413-477T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929486 | |||||||
chr18:45930008 | A | C | 1 | a0029c0046t0003g0201 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2412+668T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930008 | |||||||
chr18:45930091 | T | C | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2412+585A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930091 | |||||||
chr18:45930204 | T | C | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2412+472A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930204 | |||||||
chr18:45930212 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2412+464C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930212 | |||||||
chr18:45930472 | A | G | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2412+204T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930472 | |||||||
chr18:45930596 | A | G | 2 | a0006c0012t0006g0271 a0015c0043t0023g0047 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2412+80T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930596 | |||||||
chr18:45931477 | A | G | 2 | a0003c0003t0003g0188 a0003c0003t0003g0202 |
2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2258-647T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931477 | |||||||
chr18:45931495 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2258-665G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931495 | |||||||
chr18:45931559 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2258-729G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931559 | |||||||
chr18:45931618 | T | G | 77 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(74): Show |
81 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2258-788A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931618 | |||||||
chr18:45931698 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2258-868C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931698 | |||||||
chr18:45931766 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2258-936G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931766 | |||||||
chr18:45931767 | G | A | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2258-937C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931767 | |||||||
chr18:45932110 | C | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2258-1280G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932110 | |||||||
chr18:45932115 | G | A | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2258-1285C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932115 | |||||||
chr18:45932226 | A | C | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2258-1396T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932226 | |||||||
chr18:45932638 | T | C | 1 | a0005c0004t0005g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2258-1808A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932638 | |||||||
chr18:45932740 | T | TA | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2258-1911dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932740 | |||||||
chr18:45932745 | A | G | 1 | a0004c0025t0003g0019 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2258-1915T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932745 | |||||||
chr18:45932795 | C | T | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2258-1965G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932795 | |||||||
chr18:45932968 | CT | C | 35 | a0003c0003t0001g0185 a0003c0003t0001g0192 a0003c0003t0001g0193 others(32): Show |
36 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.2257+1840delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932968 | |||||||
chr18:45933167 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2257+1642G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933167 | |||||||
chr18:45933296 | G | A | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2257+1513C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933296 | |||||||
chr18:45933314 | G | A | 1 | a0002c0002t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2257+1495C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933314 | |||||||
chr18:45933405 | A | G | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2257+1404T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933405 | |||||||
chr18:45933431 | C | T | 1 | a0003c0003t0003g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2257+1378G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933431 | |||||||
chr18:45933669 | C | CA | 56 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0078 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.2257+1139dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933669 | |||||||
chr18:45933832 | G | A | 3 | a0002c0002t0004g0054 a0002c0002t0004g0229 a0002c0002t0026g0234 |
3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2257+977C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933832 | |||||||
chr18:45933877 | G | A | 153 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(150): Show |
159 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(156): Show |
intron_variant | MODIFIER | c.2257+932C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933877 | |||||||
chr18:45933974 | C | T | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2257+835G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933974 | |||||||
chr18:45933975 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2257+834C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933975 | |||||||
chr18:45934027 | C | T | 79 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(76): Show |
83 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2257+782G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934027 | |||||||
chr18:45934055 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2257+754C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934055 | |||||||
chr18:45934142 | A | G | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2257+667T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934142 | |||||||
chr18:45934157 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2257+652G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934157 | |||||||
chr18:45934266 | G | C | 1 | a0005c0004t0005g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2257+543C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934266 | |||||||
chr18:45934344 | C | T | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2257+465G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934344 | |||||||
chr18:45934765 | A | G | 5 | a0002c0009t0002g0275 a0002c0009t0002g0276 a0002c0009t0002g0277 others(2): Show |
5 | HG00621.hp1 HG02074.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.2257+44T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934765 | |||||||
chr18:45934784 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2257+25G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934784 | |||||||
chr18:45935010 | T | C | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2100-44A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935010 | |||||||
chr18:45935086 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2100-120A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935086 | |||||||
chr18:45935411 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
5 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-445C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935411 | |||||||
chr18:45935496 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2100-530G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935496 | |||||||
chr18:45935550 | A | G | 1 | a0002c0002t0002g0239 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2100-584T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935550 | |||||||
chr18:45935592 | CTACTAAG others(11): Show |
C | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2100-644_2100-627d others(20): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935592 | |||||||
chr18:45935610 | G | GC | 63 | a0003c0003t0001g0185 a0003c0003t0001g0192 a0003c0003t0001g0193 others(60): Show |
65 | HG00140.hp1 HG00323.hp1 HG01346.hp2 others(62): Show |
intron_variant | MODIFIER | c.2100-645_2100-644i others(3): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935610 | |||||||
chr18:45935673 | C | G | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-707G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935673 | |||||||
chr18:45935681 | G | T | 1 | a0024c0029t0001g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2100-715C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935681 | |||||||
chr18:45936142 | T | C | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2100-1176A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936142 | |||||||
chr18:45936341 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2100-1375G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936341 | |||||||
chr18:45936353 | T | A | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2100-1387A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936353 | |||||||
chr18:45936399 | T | C | 1 | a0015c0043t0023g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2100-1433A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936399 | |||||||
chr18:45936455 | CG | C | 80 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(77): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2100-1490delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936455 | |||||||
chr18:45936507 | C | A | 80 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(77): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2100-1541G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936507 | |||||||
chr18:45936568 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2100-1602T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936568 | |||||||
chr18:45936576 | A | C | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2100-1610T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936576 | |||||||
chr18:45936623 | G | A | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-1657C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936623 | |||||||
chr18:45936683 | T | C | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2100-1717A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936683 | |||||||
chr18:45936720 | C | CA | 72 | a0001c0001t0001g0061 a0002c0002t0001g0292 a0002c0002t0001g0293 others(69): Show |
75 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.2100-1755dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936720 | |||||||
chr18:45936784 | T | TA | 74 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0230 others(71): Show |
77 | HG00140.hp1 HG00323.hp1 HG01109.hp1 others(74): Show |
intron_variant | MODIFIER | c.2100-1819dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936784 | |||||||
chr18:45936784 | T | TAA | 67 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(64): Show |
70 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.2100-1820_2100-181 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936784 | |||||||
chr18:45936811 | G | A | 1 | a0002c0002t0002g0237 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2100-1845C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936811 | |||||||
chr18:45936915 | G | C | 80 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(77): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2100-1949C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936915 | |||||||
chr18:45937007 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2100-2041A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937007 | |||||||
chr18:45937065 | G | A | 113 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(110): Show |
118 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.2100-2099C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937065 | |||||||
chr18:45937110 | C | T | 1 | a0002c0002t0002g0237 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2100-2144G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937110 | |||||||
chr18:45937227 | CAT | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0086 others(5): Show |
11 | HG01169.hp2 HG01361.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2100-2263_2100-226 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937227 | |||||||
chr18:45937233 | TATACAC | T | 10 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0006c0011t0006g0039 others(7): Show |
10 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2100-2273_2100-226 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937233 | |||||||
chr18:45937235 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0009g0146 a0001c0024t0001g0164 |
3 | NA18980.hp2 NA18994.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2100-2269A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | T | TAC | 17 | a0001c0001t0001g0123 a0001c0001t0004g0082 a0005c0004t0001g0031 others(14): Show |
17 | HG00140.hp1 HG01358.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.2100-2271_2100-227 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | T | TACAC | 3 | a0005c0004t0005g0003 a0013c0026t0005g0024 a0013c0026t0005g0025 |
3 | HG01516.hp2 HG01517.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2100-2273_2100-227 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TAC | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0069 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2100-2271_2100-227 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACAC | T | 22 | a0001c0001t0001g0143 a0001c0001t0001g0161 a0001c0001t0003g0095 others(19): Show |
22 | HG00323.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2100-2273_2100-227 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACAC | T | 12 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(9): Show |
12 | HG02572.hp2 HG02886.hp2 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2100-2275_2100-227 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(1): Show |
T | 6 | a0002c0002t0001g0066 a0002c0002t0008g0063 a0002c0033t0001g0062 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100-2277_2100-227 others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(7): Show |
T | 1 | a0002c0002t0002g0262 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2100-2283_2100-227 others(18): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(9): Show |
T | 4 | a0002c0002t0030g0050 a0002c0002t0031g0049 a0011c0022t0020g0045 others(1): Show |
4 | HG01496.hp1 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2100-2285_2100-227 others(20): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(11): Show |
T | 61 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(58): Show |
64 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2100-2287_2100-227 others(22): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(13): Show |
T | 9 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 others(6): Show |
10 | HG02280.hp2 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-2289_2100-227 others(24): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(15): Show |
T | 5 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-2291_2100-227 others(26): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937235 | TACACACA others(19): Show |
T | 1 | a0002c0009t0002g0275 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2100-2295_2100-227 others(30): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | |||||||
chr18:45937237 | C | T | 5 | a0003c0003t0003g0189 a0003c0013t0001g0006 a0003c0013t0001g0204 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2100-2271G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937237 | |||||||
chr18:45937239 | C | T | 18 | a0003c0003t0001g0185 a0003c0003t0001g0192 a0003c0003t0001g0193 others(15): Show |
18 | HG01346.hp2 HG01928.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.2100-2273G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937239 | |||||||
chr18:45937241 | C | T | 9 | a0003c0003t0001g0203 a0003c0003t0003g0194 a0003c0003t0003g0196 others(6): Show |
9 | HG03239.hp2 HG03471.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.2100-2275G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937241 | |||||||
chr18:45937243 | C | T | 2 | a0027c0036t0013g0285 a0028c0028t0018g0291 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2100-2277G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937243 | |||||||
chr18:45937245 | C | T | 4 | a0003c0003t0003g0186 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2100-2279G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937245 | |||||||
chr18:45937251 | C | T | 1 | a0002c0002t0002g0262 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2100-2285G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937251 | |||||||
chr18:45937253 | C | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2100-2287G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937253 | |||||||
chr18:45937255 | C | T | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2100-2289G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937255 | |||||||
chr18:45937257 | C | T | 9 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 others(6): Show |
10 | HG02280.hp2 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-2291G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937257 | |||||||
chr18:45937259 | C | T | 5 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-2293G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937259 | |||||||
chr18:45937263 | C | T | 1 | a0002c0009t0002g0275 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2100-2297G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937263 | |||||||
chr18:45937279 | T | C | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-2313A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937279 | |||||||
chr18:45937295 | T | A | 80 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(77): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2099+2305A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937295 | |||||||
chr18:45937320 | T | TTA | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2099+2278_2099+227 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937320 | |||||||
chr18:45937327 | T | TATATACA others(11): Show |
2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2099+2255_2099+227 others(22): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937327 | |||||||
chr18:45937331 | T | C | 1 | a0030c0035t0001g0134 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2099+2269A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937331 | |||||||
chr18:45937349 | T | TACACATA others(11): Show |
2 | a0001c0001t0001g0169 a0001c0001t0036g0168 |
2 | HG02165.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2099+2233_2099+225 others(22): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937349 | |||||||
chr18:45937371 | C | T | 80 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(77): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2099+2229G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937371 | |||||||
chr18:45937374 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2099+2226T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937374 | |||||||
chr18:45937399 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2099+2201G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937399 | |||||||
chr18:45937415 | T | C | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2099+2185A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937415 | |||||||
chr18:45937470 | G | A | 66 | a0001c0001t0009g0217 a0002c0002t0002g0002 a0002c0002t0002g0007 others(63): Show |
69 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.2099+2130C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937470 | |||||||
chr18:45937586 | T | G | 2 | a0006c0012t0006g0271 a0015c0043t0023g0047 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2099+2014A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937586 | |||||||
chr18:45937670 | G | C | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2099+1930C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937670 | |||||||
chr18:45937800 | C | T | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.2099+1800G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937800 | |||||||
chr18:45937902 | T | C | 5 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2099+1698A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937902 | |||||||
chr18:45938039 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2099+1561G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938039 | |||||||
chr18:45938162 | G | A | 2 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2099+1438C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938162 | |||||||
chr18:45938182 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2099+1418G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938182 | |||||||
chr18:45938420 | C | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2099+1180G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938420 | |||||||
chr18:45938423 | C | T | 1 | a0003c0003t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2099+1177G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938423 | |||||||
chr18:45938461 | C | CA | 79 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(76): Show |
83 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2099+1138dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938461 | |||||||
chr18:45938615 | A | G | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2099+985T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938615 | |||||||
chr18:45938627 | C | G | 1 | a0005c0004t0015g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2099+973G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938627 | |||||||
chr18:45938651 | T | C | 5 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2099+949A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938651 | |||||||
chr18:45938784 | C | T | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2099+816G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938784 | |||||||
chr18:45938785 | G | A | 6 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2099+815C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938785 | |||||||
chr18:45938985 | G | A | 2 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2099+615C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938985 | |||||||
chr18:45939028 | A | T | 1 | a0004c0014t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2099+572T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939028 | |||||||
chr18:45939313 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2099+287A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939313 | |||||||
chr18:45939408 | G | A | 1 | a0008c0008t0002g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2099+192C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939408 | |||||||
chr18:45939475 | A | G | 114 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(111): Show |
119 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.2099+125T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939475 | |||||||
chr18:45939807 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0172 |
2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1944-52G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45939807 | |||||||
chr18:45939859 | C | T | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1944-104G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45939859 | |||||||
chr18:45940012 | G | A | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1944-257C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940012 | |||||||
chr18:45940113 | G | C | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1944-358C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940113 | |||||||
chr18:45940203 | C | T | 4 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944-448G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940203 | |||||||
chr18:45940248 | G | A | 84 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(81): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1944-493C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940248 | |||||||
chr18:45940299 | C | T | 1 | a0001c0001t0004g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1944-544G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940299 | |||||||
chr18:45940313 | C | T | 1 | a0009c0007t0007g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1944-558G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940313 | |||||||
chr18:45940334 | C | T | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1944-579G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940334 | |||||||
chr18:45940463 | C | T | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1944-708G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940463 | |||||||
chr18:45940493 | AT | A | 6 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944-739delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940493 | |||||||
chr18:45940620 | A | G | 6 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944-865T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940620 | |||||||
chr18:45940629 | G | A | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1944-874C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940629 | |||||||
chr18:45940902 | G | C | 29 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0081 others(26): Show |
29 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1944-1147C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940902 | |||||||
chr18:45941001 | G | C | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1944-1246C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941001 | |||||||
chr18:45941285 | G | A | 1 | a0005c0004t0015g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1944-1530C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941285 | |||||||
chr18:45941309 | G | A | 37 | a0001c0001t0002g0187 a0002c0002t0003g0184 a0003c0003t0001g0185 others(34): Show |
38 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1944-1554C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941309 | |||||||
chr18:45941639 | T | C | 6 | a0007c0006t0003g0210 a0007c0006t0003g0211 a0007c0006t0003g0212 others(3): Show |
6 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1943+1522A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941639 | |||||||
chr18:45941946 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1943+1215C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941946 | |||||||
chr18:45941993 | G | A | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+1168C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941993 | |||||||
chr18:45942019 | T | C | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+1142A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942019 | |||||||
chr18:45942094 | A | G | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+1067T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942094 | |||||||
chr18:45942118 | G | A | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1943+1043C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942118 | |||||||
chr18:45942258 | C | T | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1943+903G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942258 | |||||||
chr18:45942280 | T | C | 1 | a0008c0008t0002g0023 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1943+881A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942280 | |||||||
chr18:45942385 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1943+776A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942385 | |||||||
chr18:45942393 | A | G | 1 | a0002c0002t0038g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1943+768T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942393 | |||||||
chr18:45942465 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1943+696A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942465 | |||||||
chr18:45942480 | G | A | 1 | a0002c0002t0002g0269 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1943+681C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942480 | |||||||
chr18:45942524 | AC | A | 37 | a0001c0001t0002g0187 a0002c0002t0003g0184 a0003c0003t0001g0185 others(34): Show |
38 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1943+636delG | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942524 | |||||||
chr18:45942535 | G | A | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+626C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942535 | |||||||
chr18:45942557 | C | T | 1 | a0002c0002t0002g0269 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1943+604G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942557 | |||||||
chr18:45942558 | G | A | 1 | a0004c0025t0003g0019 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1943+603C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942558 | |||||||
chr18:45942766 | A | G | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1943+395T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942766 | |||||||
chr18:45943107 | T | C | 1 | a0006c0012t0006g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1943+54A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45943107 | |||||||
chr18:45943139 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1943+22C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45943139 | |||||||
chr18:45943346 | G | A | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1793-35C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943346 | |||||||
chr18:45943475 | G | T | 1 | a0015c0042t0022g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1793-164C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943475 | |||||||
chr18:45943499 | A | G | 1 | a0001c0001t0040g0141 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1793-188T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943499 | |||||||
chr18:45943520 | T | G | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1793-209A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943520 | |||||||
chr18:45943605 | A | G | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1793-294T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943605 | |||||||
chr18:45943606 | C | T | 1 | a0006c0011t0013g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1793-295G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943606 | |||||||
chr18:45943609 | G | A | 2 | a0001c0021t0001g0136 a0001c0021t0004g0137 |
2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1793-298C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943609 | |||||||
chr18:45943732 | T | A | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1792+273A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943732 | |||||||
chr18:45943794 | G | A | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1792+211C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943794 | |||||||
chr18:45943853 | A | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1792+152T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943853 | |||||||
chr18:45944179 | C | A | 26 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(23): Show |
27 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.1678-60G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944179 | |||||||
chr18:45944273 | G | T | 2 | a0002c0002t0017g0228 a0006c0012t0006g0226 |
2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1678-154C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944273 | |||||||
chr18:45944332 | A | G | 23 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(20): Show |
24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1678-213T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944332 | |||||||
chr18:45944426 | T | C | 1 | a0027c0036t0013g0285 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1678-307A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944426 | |||||||
chr18:45944483 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1678-364C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944483 | |||||||
chr18:45944511 | T | C | 2 | a0013c0026t0005g0024 a0013c0026t0005g0025 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1678-392A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944511 | |||||||
chr18:45944674 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1678-555C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944674 | |||||||
chr18:45944687 | G | A | 90 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(87): Show |
94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1678-568C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944687 | |||||||
chr18:45944727 | G | C | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1678-608C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944727 | |||||||
chr18:45944741 | C | T | 1 | a0005c0004t0015g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1678-622G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944741 | |||||||
chr18:45944879 | G | A | 1 | a0002c0002t0002g0263 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1678-760C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944879 | |||||||
chr18:45945479 | G | T | 1 | a0015c0042t0022g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1677+1184C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945479 | |||||||
chr18:45945608 | C | T | 1 | a0026c0041t0007g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1677+1055G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945608 | |||||||
chr18:45945772 | T | C | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1677+891A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945772 | |||||||
chr18:45945845 | G | A | 67 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(64): Show |
70 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.1677+818C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945845 | |||||||
chr18:45945852 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1677+811C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945852 | |||||||
chr18:45945854 | G | A | 9 | a0003c0003t0003g0194 a0003c0003t0003g0196 a0003c0003t0003g0198 others(6): Show |
9 | NA18944.hp2 NA18948.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+809C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945854 | |||||||
chr18:45946081 | C | A | 151 | a0001c0001t0001g0038 a0001c0001t0002g0187 a0002c0002t0001g0292 others(148): Show |
157 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.1677+582G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946081 | |||||||
chr18:45946097 | T | C | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1677+566A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946097 | |||||||
chr18:45946321 | A | C | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1677+342T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946321 | |||||||
chr18:45946333 | C | T | 1 | a0005c0004t0005g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1677+330G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946333 | |||||||
chr18:45946532 | A | G | 2 | a0001c0001t0004g0119 a0001c0001t0004g0120 |
2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1677+131T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946532 | |||||||
chr18:45946806 | T | C | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1572-38A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45946806 | |||||||
chr18:45947012 | C | T | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1572-244G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947012 | |||||||
chr18:45947131 | G | C | 1 | a0002c0002t0024g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1572-363C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947131 | |||||||
chr18:45947285 | T | C | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572-517A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947285 | |||||||
chr18:45947393 | A | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1572-625T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947393 | |||||||
chr18:45947406 | C | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1572-638G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947406 | |||||||
chr18:45947435 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0138 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572-667C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947435 | |||||||
chr18:45947441 | C | G | 2 | a0001c0001t0001g0118 a0025c0045t0001g0117 |
2 | HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1572-673G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947441 | |||||||
chr18:45947506 | C | T | 3 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 |
3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1572-738G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947506 | |||||||
chr18:45947775 | CT | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0128 a0006c0011t0006g0039 others(4): Show |
7 | HG00140.hp2 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1571+727delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947775 | |||||||
chr18:45947814 | G | A | 1 | a0001c0001t0032g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1571+689C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947814 | |||||||
chr18:45947835 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1571+668G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947835 | |||||||
chr18:45947935 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1571+568G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947935 | |||||||
chr18:45948015 | T | G | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1571+488A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948015 | |||||||
chr18:45948167 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1571+336C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948167 | |||||||
chr18:45948283 | A | G | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1571+220T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948283 | |||||||
chr18:45948382 | A | C | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1571+121T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948382 | |||||||
chr18:45948396 | A | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1571+107T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948396 | |||||||
chr18:45948741 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1498-165G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/43 | chr18 | 45948741 | |||||||
chr18:45949417 | C | T | 4 | a0006c0011t0006g0039 a0006c0011t0006g0041 a0006c0011t0006g0042 others(1): Show |
4 | HG01884.hp1 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+67G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/43 | chr18 | 45949417 | |||||||
chr18:45949449 | C | T | 3 | a0005c0004t0005g0026 a0005c0004t0005g0027 a0005c0004t0005g0028 |
3 | HG02257.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1497+35G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/43 | chr18 | 45949449 | |||||||
chr18:45949869 | C | T | 1 | a0003c0003t0003g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1390-278G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949869 | |||||||
chr18:45949884 | A | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1390-293T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949884 | |||||||
chr18:45949966 | T | C | 1 | a0001c0001t0032g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1390-375A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949966 | |||||||
chr18:45949977 | A | T | 31 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(28): Show |
33 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.1390-386T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949977 | |||||||
chr18:45950016 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(66): Show |
72 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1390-425A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950016 | |||||||
chr18:45950124 | C | T | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-533G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950124 | |||||||
chr18:45950153 | T | C | 1 | a0003c0003t0003g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1390-562A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950153 | |||||||
chr18:45950184 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1390-593G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950184 | |||||||
chr18:45950239 | T | C | 1 | a0017c0019t0006g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1390-648A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950239 | |||||||
chr18:45950377 | C | T | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389+725G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950377 | |||||||
chr18:45950378 | G | A | 6 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+724C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950378 | |||||||
chr18:45950491 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1389+611C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950491 | |||||||
chr18:45950504 | C | T | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1389+598G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950504 | |||||||
chr18:45950614 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1389+488G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950614 | |||||||
chr18:45950759 | A | G | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389+343T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950759 | |||||||
chr18:45950935 | G | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1389+167C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950935 | |||||||
chr18:45950966 | AAAG | A | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1389+133_1389+135d others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950966 | |||||||
chr18:45951275 | T | C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01169.hp1 HG01243.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253-37A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951275 | |||||||
chr18:45951283 | T | C | 1 | a0002c0002t0002g0265 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1253-45A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951283 | |||||||
chr18:45951344 | G | A | 2 | a0002c0009t0002g0275 a0002c0009t0002g0276 |
2 | NA18964.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1253-106C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951344 | |||||||
chr18:45951385 | T | G | 1 | a0003c0003t0003g0208 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1253-147A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951385 | |||||||
chr18:45951398 | C | T | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1253-160G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951398 | |||||||
chr18:45951399 | A | C | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1253-161T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951399 | |||||||
chr18:45951436 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1253-198A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951436 | |||||||
chr18:45951461 | AT | A | 86 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(83): Show |
89 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1253-224delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951461 | |||||||
chr18:45951461 | ATTT | A | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1253-226_1253-224d others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951461 | |||||||
chr18:45951510 | A | G | 30 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(27): Show |
31 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1253-272T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951510 | |||||||
chr18:45951527 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA18957.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1253-289A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951527 | |||||||
chr18:45951545 | G | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(66): Show |
72 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1253-307C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951545 | |||||||
chr18:45951674 | A | G | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1253-436T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951674 | |||||||
chr18:45951675 | T | C | 1 | a0006c0011t0013g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1253-437A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951675 | |||||||
chr18:45951735 | A | G | 1 | a0003c0044t0003g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1253-497T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951735 | |||||||
chr18:45951736 | G | C | 1 | a0002c0040t0002g0266 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1253-498C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951736 | |||||||
chr18:45951902 | A | G | 60 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(57): Show |
63 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1252+498T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951902 | |||||||
chr18:45951903 | A | G | 60 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(57): Show |
63 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1252+497T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951903 | |||||||
chr18:45952769 | G | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1009-126C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45952769 | |||||||
chr18:45952940 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1009-297C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45952940 | |||||||
chr18:45952956 | G | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1009-313C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45952956 | |||||||
chr18:45953027 | G | T | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1009-384C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953027 | |||||||
chr18:45953117 | G | A | 1 | a0006c0012t0006g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1009-474C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953117 | |||||||
chr18:45953129 | C | T | 1 | a0005c0004t0015g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1009-486G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953129 | |||||||
chr18:45953152 | G | A | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009-509C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953152 | |||||||
chr18:45953254 | C | A | 85 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(82): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1009-611G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953254 | |||||||
chr18:45953498 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1009-855A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953498 | |||||||
chr18:45953904 | ACT | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1008+488_1008+489d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953904 | |||||||
chr18:45953955 | T | C | 71 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(68): Show |
74 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1008+439A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953955 | |||||||
chr18:45954077 | T | C | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1008+317A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45954077 | |||||||
chr18:45954327 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1008+67G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45954327 | |||||||
chr18:45954346 | A | G | 1 | a0018c0017t0010g0222 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1008+48T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45954346 | |||||||
chr18:45955398 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64-60T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955398 | |||||||
chr18:45955537 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-199C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955537 | |||||||
chr18:45955551 | T | C | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-213A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955551 | |||||||
chr18:45955617 | A | G | 1 | a0025c0045t0001g0117 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.64-279T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955617 | |||||||
chr18:45955661 | G | A | 64 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(61): Show |
67 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-323C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955661 | |||||||
chr18:45955673 | A | G | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-335T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955673 | |||||||
chr18:45955782 | T | C | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-444A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955782 | |||||||
chr18:45955883 | A | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-545T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955883 | |||||||
chr18:45956018 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-680C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956018 | |||||||
chr18:45956019 | G | A | 1 | a0015c0043t0023g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-681C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956019 | |||||||
chr18:45956074 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-736G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956074 | |||||||
chr18:45956090 | A | T | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-752T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956090 | |||||||
chr18:45956294 | C | T | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-956G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956294 | |||||||
chr18:45956336 | C | A | 1 | a0004c0005t0033g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-998G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956336 | |||||||
chr18:45956368 | A | T | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1030T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956368 | |||||||
chr18:45956461 | A | AT | 6 | a0003c0003t0001g0203 a0003c0013t0001g0006 a0003c0013t0001g0204 others(3): Show |
7 | HG02145.hp1 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1124dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956461 | |||||||
chr18:45956461 | A | ATTTAT | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1124_64-1123ins others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956461 | |||||||
chr18:45956465 | T | A | 81 | a0001c0001t0001g0079 a0002c0002t0001g0292 a0002c0002t0001g0293 others(78): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.64-1127A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956465 | |||||||
chr18:45956469 | T | A | 3 | a0002c0002t0008g0051 a0019c0016t0010g0224 a0019c0016t0010g0225 |
3 | HG03209.hp2 HG03453.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.64-1131A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956469 | |||||||
chr18:45956469 | T | C | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1131A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956469 | |||||||
chr18:45956480 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1142C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956480 | |||||||
chr18:45956518 | G | A | 1 | a0002c0002t0002g0268 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.64-1180C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956518 | |||||||
chr18:45956545 | C | T | 85 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(82): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-1207G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956545 | |||||||
chr18:45956607 | A | G | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-1269T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956607 | |||||||
chr18:45956608 | C | A | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1270G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956608 | |||||||
chr18:45956726 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1388C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956726 | |||||||
chr18:45956775 | C | T | 1 | a0001c0001t0003g0116 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.64-1437G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956775 | |||||||
chr18:45956882 | A | T | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-1544T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956882 | |||||||
chr18:45956899 | T | TA | 115 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(112): Show |
120 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.64-1562dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956899 | |||||||
chr18:45956913 | T | C | 1 | a0002c0002t0017g0228 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-1575A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956913 | |||||||
chr18:45957144 | C | T | 5 | a0009c0007t0007g0008 a0009c0007t0007g0012 a0009c0007t0007g0013 others(2): Show |
6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1806G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957144 | |||||||
chr18:45957179 | T | C | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-1841A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957179 | |||||||
chr18:45957203 | A | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1865T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957203 | |||||||
chr18:45957287 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1949A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957287 | |||||||
chr18:45957309 | T | C | 28 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(25): Show |
30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1971A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957309 | |||||||
chr18:45957363 | A | T | 5 | a0008c0008t0002g0021 a0008c0008t0002g0022 a0008c0008t0002g0023 others(2): Show |
5 | HG01358.hp2 HG02071.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-2025T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957363 | |||||||
chr18:45957419 | A | G | 11 | a0002c0002t0001g0066 a0002c0002t0001g0068 a0002c0002t0002g0064 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-2081T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957419 | |||||||
chr18:45957601 | G | A | 4 | a0001c0001t0032g0115 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2263C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957601 | |||||||
chr18:45957821 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-2483A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957821 | |||||||
chr18:45957825 | A | G | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-2487T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957825 | |||||||
chr18:45958185 | A | T | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.64-2847T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958185 | |||||||
chr18:45958366 | A | C | 32 | a0001c0001t0002g0187 a0002c0002t0003g0184 a0003c0003t0001g0185 others(29): Show |
32 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.64-3028T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958366 | |||||||
chr18:45958369 | C | A | 2 | a0001c0001t0001g0169 a0001c0001t0036g0168 |
2 | HG02165.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.64-3031G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958369 | |||||||
chr18:45958425 | C | T | 1 | a0001c0034t0001g0089 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-3087G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958425 | |||||||
chr18:45958439 | A | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3101T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958439 | |||||||
chr18:45958444 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3106A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958444 | |||||||
chr18:45958469 | G | GGACA | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-3135_64-3132dup others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958469 | |||||||
chr18:45958575 | G | A | 1 | a0008c0008t0002g0036 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.64-3237C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958575 | |||||||
chr18:45958709 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3371C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958709 | |||||||
chr18:45958843 | T | C | 6 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-3505A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958843 | |||||||
chr18:45958870 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3532A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958870 | |||||||
chr18:45959008 | A | C | 1 | a0005c0048t0003g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-3670T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959008 | |||||||
chr18:45959008 | A | T | 6 | a0005c0004t0015g0017 a0009c0007t0007g0008 a0009c0007t0007g0012 others(3): Show |
7 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3670T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959008 | |||||||
chr18:45959009 | A | T | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3671T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959009 | |||||||
chr18:45959010 | G | GGGGGTT | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3673_64-3672ins others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959010 | |||||||
chr18:45959040 | C | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0121 others(12): Show |
16 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-3702G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959040 | |||||||
chr18:45959057 | A | G | 1 | a0005c0004t0004g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64-3719T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959057 | |||||||
chr18:45959060 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64-3722T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959060 | |||||||
chr18:45959230 | A | T | 1 | a0004c0005t0034g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64-3892T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959230 | |||||||
chr18:45959275 | A | C | 4 | a0018c0017t0010g0222 a0018c0017t0010g0223 a0019c0016t0010g0224 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-3937T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959275 | |||||||
chr18:45959290 | G | A | 2 | a0003c0003t0003g0207 a0003c0003t0003g0208 |
2 | NA18957.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.64-3952C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959290 | |||||||
chr18:45959324 | G | A | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3986C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959324 | |||||||
chr18:45959339 | T | C | 3 | a0002c0002t0017g0228 a0002c0002t0029g0227 a0006c0012t0006g0226 |
3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.64-4001A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959339 | |||||||
chr18:45959363 | GGGCCA | G | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-4030_64-4026del others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959363 | |||||||
chr18:45959368 | A | G | 113 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(110): Show |
118 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.64-4030T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959368 | |||||||
chr18:45959386 | C | A | 1 | a0001c0001t0004g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.64-4048G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959386 | |||||||
chr18:45959418 | AG | A | 5 | a0002c0002t0014g0219 a0006c0012t0006g0220 a0006c0012t0006g0221 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4081delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959418 | |||||||
chr18:45959532 | G | C | 10 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-4194C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959532 | |||||||
chr18:45959658 | C | CTAAA | 69 | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0001g0074 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-4324_64-4321dup others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | |||||||
chr18:45959658 | CTAAA | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0038 others(115): Show |
124 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.64-4324_64-4321del others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | |||||||
chr18:45959658 | CTAAATAA others(1): Show |
C | 10 | a0002c0002t0002g0230 a0002c0002t0002g0231 a0002c0002t0002g0283 others(7): Show |
11 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-4328_64-4321del others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | |||||||
chr18:45959658 | CTAAATAA others(5): Show |
C | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-4332_64-4321del others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | |||||||
chr18:45959703 | G | A | 85 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(82): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-4365C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959703 | |||||||
chr18:45959705 | T | C | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-4367A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959705 | |||||||
chr18:45959836 | G | A | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-4498C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959836 | |||||||
chr18:45959948 | T | C | 7 | a0005c0004t0015g0017 a0005c0048t0003g0018 a0009c0007t0007g0008 others(4): Show |
8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4610A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959948 | |||||||
chr18:45960023 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-4685T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960023 | |||||||
chr18:45960240 | A | G | 1 | a0002c0002t0004g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64-4902T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960240 | |||||||
chr18:45960425 | C | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0142 others(34): Show |
40 | HG00609.hp1 HG01109.hp2 HG02074.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-5087G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960425 | |||||||
chr18:45960526 | T | TA | 31 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(28): Show |
33 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-5189dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960526 | |||||||
chr18:45960533 | C | T | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-5195G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960533 | |||||||
chr18:45960583 | A | G | 68 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(65): Show |
71 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-5245T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960583 | |||||||
chr18:45960590 | TGATA | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-5256_64-5253del others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960590 | |||||||
chr18:45960715 | T | C | 3 | a0014c0015t0014g0289 a0014c0015t0019g0290 a0028c0028t0018g0291 |
3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-5377A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960715 | |||||||
chr18:45960720 | T | G | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-5382A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960720 | |||||||
chr18:45961289 | C | T | 27 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(24): Show |
28 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.63+5888G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961289 | |||||||
chr18:45961290 | C | T | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5887G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961290 | |||||||
chr18:45961635 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.63+5542G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961635 | |||||||
chr18:45961858 | C | CA | 46 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0172 others(43): Show |
47 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+5318dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961858 | |||||||
chr18:45962031 | T | A | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5146A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962031 | |||||||
chr18:45962067 | GT | G | 65 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0002g0002 others(62): Show |
68 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.63+5109delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962067 | |||||||
chr18:45962108 | G | A | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5069C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962108 | |||||||
chr18:45962142 | A | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5035T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962142 | |||||||
chr18:45962209 | A | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+4968T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962209 | |||||||
chr18:45962322 | T | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+4855A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962322 | |||||||
chr18:45962348 | T | C | 31 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(28): Show |
33 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.63+4829A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962348 | |||||||
chr18:45962527 | C | T | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+4650G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962527 | |||||||
chr18:45962598 | C | T | 116 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(113): Show |
121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+4579G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962598 | |||||||
chr18:45962821 | T | C | 1 | a0002c0002t0002g0270 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+4356A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962821 | |||||||
chr18:45962823 | G | A | 59 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0052 others(56): Show |
62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.63+4354C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962823 | |||||||
chr18:45963018 | T | A | 1 | a0002c0002t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+4159A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963018 | |||||||
chr18:45963058 | G | A | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+4119C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963058 | |||||||
chr18:45963060 | C | T | 2 | a0002c0009t0002g0275 a0002c0009t0002g0276 |
2 | NA18964.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.63+4117G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963060 | |||||||
chr18:45963067 | T | G | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+4110A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963067 | |||||||
chr18:45963254 | C | T | 1 | a0004c0005t0003g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+3923G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963254 | |||||||
chr18:45963262 | T | G | 1 | a0002c0002t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+3915A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963262 | |||||||
chr18:45963273 | C | T | 34 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0078 others(31): Show |
34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.63+3904G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963273 | |||||||
chr18:45963334 | A | G | 2 | a0001c0001t0001g0061 a0024c0029t0001g0060 |
2 | HG01169.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.63+3843T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963334 | |||||||
chr18:45963359 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.63+3818T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963359 | |||||||
chr18:45963372 | G | C | 37 | a0001c0001t0002g0187 a0002c0002t0003g0184 a0003c0003t0001g0185 others(34): Show |
38 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.63+3805C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963372 | |||||||
chr18:45963409 | G | C | 21 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(18): Show |
22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+3768C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963409 | |||||||
chr18:45963442 | G | A | 1 | a0005c0004t0009g0037 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.63+3735C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963442 | |||||||
chr18:45963453 | G | A | 3 | a0001c0001t0004g0180 a0001c0001t0011g0181 a0001c0001t0011g0182 |
3 | HG01261.hp1 HG02293.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.63+3724C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963453 | |||||||
chr18:45963465 | C | T | 6 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3712G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963465 | |||||||
chr18:45963613 | T | G | 2 | a0011c0022t0020g0045 a0011c0022t0021g0046 |
2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.63+3564A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963613 | |||||||
chr18:45963665 | T | G | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3512A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963665 | |||||||
chr18:45963719 | A | G | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3458T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963719 | |||||||
chr18:45963727 | T | A | 85 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(82): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+3450A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963727 | |||||||
chr18:45963794 | A | G | 1 | a0001c0001t0043g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.63+3383T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963794 | |||||||
chr18:45963798 | T | A | 1 | a0002c0002t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+3379A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963798 | |||||||
chr18:45963872 | G | C | 1 | a0005c0004t0009g0037 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.63+3305C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963872 | |||||||
chr18:45963898 | G | A | 154 | a0001c0001t0001g0038 a0001c0001t0002g0187 a0002c0002t0001g0292 others(151): Show |
160 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(157): Show |
intron_variant | MODIFIER | c.63+3279C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963898 | |||||||
chr18:45964031 | C | T | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3146G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964031 | |||||||
chr18:45964115 | T | C | 4 | a0001c0001t0001g0214 a0001c0001t0004g0215 a0001c0001t0009g0217 others(1): Show |
4 | HG00438.hp1 HG00621.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3062A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964115 | |||||||
chr18:45964191 | T | TTC | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2985_63+2986ins others(2): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964191 | |||||||
chr18:45964209 | A | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2968T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964209 | |||||||
chr18:45964239 | T | G | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2938A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964239 | |||||||
chr18:45964270 | G | A | 85 | a0001c0001t0001g0038 a0002c0002t0001g0292 a0002c0002t0001g0293 others(82): Show |
88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+2907C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964270 | |||||||
chr18:45964302 | T | A | 1 | a0002c0002t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+2875A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964302 | |||||||
chr18:45964552 | C | G | 1 | a0001c0001t0004g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63+2625G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964552 | |||||||
chr18:45964555 | T | C | 2 | a0006c0012t0006g0271 a0015c0043t0023g0047 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+2622A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964555 | |||||||
chr18:45964827 | C | G | 1 | a0003c0003t0016g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+2350G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964827 | |||||||
chr18:45964874 | A | C | 1 | a0002c0002t0002g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.63+2303T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964874 | |||||||
chr18:45964907 | CG | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2269delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964907 | |||||||
chr18:45964910 | G | A | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2267C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964910 | |||||||
chr18:45965001 | T | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2176A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965001 | |||||||
chr18:45965051 | A | G | 1 | a0002c0002t0004g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+2126T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965051 | |||||||
chr18:45965110 | T | G | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+2067A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965110 | |||||||
chr18:45965140 | TC | T | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2036delG | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965140 | |||||||
chr18:45965145 | T | A | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2032A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965145 | |||||||
chr18:45965223 | CACTT | C | 27 | a0005c0004t0001g0031 a0005c0004t0003g0033 a0005c0004t0004g0015 others(24): Show |
28 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.63+1950_63+1953del others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965223 | |||||||
chr18:45965303 | A | G | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1874T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965303 | |||||||
chr18:45965308 | G | T | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1869C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965308 | |||||||
chr18:45965320 | G | T | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1857C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965320 | |||||||
chr18:45965346 | C | T | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1831G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965346 | |||||||
chr18:45965458 | G | A | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+1719C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965458 | |||||||
chr18:45965773 | G | T | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+1404C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965773 | |||||||
chr18:45965940 | T | C | 3 | a0002c0002t0002g0272 a0002c0002t0002g0273 a0002c0002t0008g0274 |
3 | HG01071.hp2 HG01192.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.63+1237A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965940 | |||||||
chr18:45966053 | T | C | 2 | a0005c0004t0015g0017 a0005c0048t0003g0018 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.63+1124A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966053 | |||||||
chr18:45966094 | T | C | 5 | a0002c0009t0002g0275 a0002c0009t0002g0276 a0002c0009t0002g0277 others(2): Show |
5 | HG00621.hp1 HG02074.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+1083A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966094 | |||||||
chr18:45966098 | C | T | 1 | a0002c0002t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+1079G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966098 | |||||||
chr18:45966150 | A | C | 1 | a0002c0002t0002g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.63+1027T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966150 | |||||||
chr18:45966244 | C | T | 1 | a0002c0002t0008g0051 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+933G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966244 | |||||||
chr18:45966265 | G | C | 22 | a0004c0025t0003g0019 a0005c0004t0001g0031 a0005c0004t0003g0033 others(19): Show |
23 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+912C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966265 | |||||||
chr18:45966324 | C | T | 3 | a0002c0002t0030g0050 a0002c0002t0031g0049 a0004c0005t0033g0048 |
3 | HG02615.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.63+853G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966324 | |||||||
chr18:45966375 | C | CA | 32 | a0001c0001t0001g0281 a0002c0002t0002g0280 a0002c0002t0002g0283 others(29): Show |
33 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.63+801dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966375 | |||||||
chr18:45966391 | A | T | 4 | a0011c0022t0020g0045 a0011c0022t0021g0046 a0015c0042t0022g0044 others(1): Show |
4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+786T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966391 | |||||||
chr18:45966421 | T | C | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+756A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966421 | |||||||
chr18:45966442 | A | ATGTATAT others(21): Show |
6 | a0001c0001t0001g0038 a0006c0011t0006g0039 a0006c0011t0006g0041 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+707_63+734dupCA others(26): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966442 | |||||||
chr18:45966457 | CATATGTA others(11): Show |
C | 2 | a0007c0006t0003g0287 a0007c0006t0003g0288 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.63+702_63+719delAT others(16): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966457 | |||||||
chr18:45966543 | T | C | 4 | a0009c0007t0007g0008 a0014c0015t0014g0289 a0014c0015t0019g0290 others(1): Show |
5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+634A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966543 | |||||||
chr18:45966569 | C | T | 28 | a0004c0025t0003g0019 a0005c0004t0001g0031 a0005c0004t0003g0033 others(25): Show |
29 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.63+608G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966569 | |||||||
chr18:45966716 | G | A | 1 | a0028c0028t0018g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+461C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966716 | |||||||
chr18:45966727 | A | T | 1 | a0002c0038t0007g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+450T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966727 | |||||||
chr18:45966988 | G | C | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0037g0294 |
3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+189C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966988 |