Item | Value |
---|---|
geneid | 57493 |
ensemblid | ENSG00000173706.15 |
hgncid | 29227 |
symbol | HEG1 |
name | heart development protein with EGF like domains 1 |
refseq_nuc | NM_020733.2 |
refseq_prot | NP_065784.1 |
ensembl_nuc | ENST00000311127.9 |
ensembl_prot | ENSP00000311502.3 |
mane_status | MANE Select |
chr | chr3 |
start | 124965710 |
end | 125055997 |
strand | - |
ver | v1.2 |
region | chr3:124965710-125055997 |
region5000 | chr3:124960710-125060997 |
regionname0 | HEG1_chr3_124965710_125055997 |
regionname5000 | HEG1_chr3_124960710_125060997 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1381 | 106 | 8 | 21 | 52 | 3 | 21 | 41 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0002 | 0/0 | 1387 | 60 | 10 | 3 | 42 | 0 | 5 | 34 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0003 | 1/0 | 1381 | 29 | 6 | 2 | 16 | 1 | 3 | 13 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0004 | 0/0 | 1387 | 22 | 9 | 4 | 9 | 0 | 0 | 5 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0005 | 0/0 | 1381 | 16 | 4 | 3 | 7 | 1 | 1 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0006 | 0/0 | 1381 | 13 | 5 | 3 | 3 | 0 | 2 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0007 | 0/0 | 1386 | 11 | 1 | 2 | 8 | 0 | 0 | 7 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1381): Show |
chr3 | 124960710 | 125060997 |
a0008 | 0/0 | 1381 | 10 | 2 | 5 | 3 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0009 | 0/0 | 1380 | 9 | 0 | 2 | 7 | 0 | 0 | 5 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1375): Show |
chr3 | 124960710 | 125060997 |
a0010 | 0/0 | 1381 | 7 | 0 | 5 | 0 | 0 | 2 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0011 | 0/0 | 1381 | 6 | 1 | 4 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0012 | 0/0 | 1382 | 6 | 1 | 0 | 4 | 1 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1377): Show |
chr3 | 124960710 | 125060997 |
a0013 | 0/0 | 1387 | 5 | 0 | 2 | 2 | 1 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0014 | 0/0 | 1388 | 4 | 0 | 3 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1383): Show |
chr3 | 124960710 | 125060997 |
a0015 | 0/0 | 1380 | 4 | 1 | 0 | 3 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1375): Show |
chr3 | 124960710 | 125060997 |
a0016 | 0/0 | 1381 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0017 | 0/0 | 1382 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1377): Show |
chr3 | 124960710 | 125060997 |
a0018 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0019 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0020 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0021 | 0/0 | 1381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0022 | 0/0 | 1381 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0023 | 0/0 | 1388 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1383): Show |
chr3 | 124960710 | 125060997 |
a0024 | 0/0 | 1381 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0025 | 0/0 | 1381 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0026 | 0/0 | 1380 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1375): Show |
chr3 | 124960710 | 125060997 |
a0027 | 0/0 | 1381 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0028 | 0/0 | 1381 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0029 | 0/0 | 1381 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0030 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0031 | 0/0 | 1381 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0032 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0033 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0034 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1375): Show |
chr3 | 124960710 | 125060997 |
a0035 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0036 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0037 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0038 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0039 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0040 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0041 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0042 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0043 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0044 | 0/0 | 1381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0045 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0046 | 0/0 | 1381 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1376): Show |
chr3 | 124960710 | 125060997 |
a0047 | 0/0 | 1387 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0048 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0049 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
a0050 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | MASPR others(1382): Show |
chr3 | 124960710 | 125060997 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4143 | 48 | 5 | 7 | 32 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0001c0002 | 0/1 | 4143 | 48 | 1 | 11 | 18 | 3 | 14 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0001c0010 | 0/0 | 4143 | 6 | 0 | 1 | 2 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0001c0020 | 0/0 | 4143 | 3 | 2 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0001c0085 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0003 | 0/0 | 4161 | 27 | 1 | 1 | 22 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0005 | 0/0 | 4161 | 15 | 3 | 1 | 11 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0014 | 0/0 | 4161 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0028 | 0/0 | 4161 | 2 | 0 | 0 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0033 | 0/0 | 4161 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0035 | 0/0 | 4161 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0044 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0048 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0049 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0071 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0074 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0081 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0002c0082 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0003c0004 | 0/0 | 4143 | 24 | 6 | 1 | 16 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0003c0034 | 1/0 | 4143 | 2 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0003c0045 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0003c0067 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0003c0068 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0004c0007 | 0/0 | 4161 | 13 | 5 | 3 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0004c0038 | 0/0 | 4161 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0004c0039 | 0/0 | 4161 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0004c0040 | 0/0 | 4161 | 2 | 1 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0004c0042 | 0/0 | 4161 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0004c0089 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0005c0006 | 0/0 | 4143 | 15 | 3 | 3 | 7 | 1 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0005c0086 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0006c0011 | 0/0 | 4143 | 6 | 3 | 2 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0006c0015 | 0/0 | 4143 | 5 | 0 | 1 | 3 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0006c0076 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0006c0077 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0007c0012 | 0/0 | 4158 | 5 | 0 | 0 | 5 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4153): Show |
chr3 | 124960710 | 125060997 | ||
a0007c0013 | 0/0 | 4158 | 5 | 0 | 2 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4153): Show |
chr3 | 124960710 | 125060997 | ||
a0007c0060 | 0/0 | 4158 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4153): Show |
chr3 | 124960710 | 125060997 | ||
a0008c0009 | 0/0 | 4143 | 7 | 2 | 3 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0008c0027 | 0/0 | 4143 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0009c0016 | 0/0 | 4140 | 4 | 0 | 0 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0009c0022 | 0/0 | 4140 | 3 | 0 | 2 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0009c0056 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0009c0062 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0010c0008 | 0/0 | 4143 | 7 | 0 | 5 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0011c0018 | 0/0 | 4143 | 4 | 1 | 2 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0011c0041 | 0/0 | 4143 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0012c0019 | 0/0 | 4146 | 4 | 0 | 0 | 4 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4141): Show |
chr3 | 124960710 | 125060997 | ||
a0012c0030 | 0/0 | 4146 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4141): Show |
chr3 | 124960710 | 125060997 | ||
a0013c0017 | 0/0 | 4161 | 4 | 0 | 2 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0013c0087 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0014c0053 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4159): Show |
chr3 | 124960710 | 125060997 | ||
a0014c0054 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4159): Show |
chr3 | 124960710 | 125060997 | ||
a0014c0055 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4159): Show |
chr3 | 124960710 | 125060997 | ||
a0014c0097 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4159): Show |
chr3 | 124960710 | 125060997 | ||
a0015c0021 | 0/0 | 4140 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0015c0057 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0016c0025 | 0/0 | 4143 | 3 | 1 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0017c0029 | 0/0 | 4146 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4141): Show |
chr3 | 124960710 | 125060997 | ||
a0017c0052 | 0/0 | 4146 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4141): Show |
chr3 | 124960710 | 125060997 | ||
a0018c0037 | 0/0 | 4143 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0018c0088 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0019c0026 | 0/0 | 4143 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0020c0043 | 0/0 | 4143 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0020c0096 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0021c0023 | 0/0 | 4143 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0022c0024 | 0/0 | 4143 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0023c0031 | 0/0 | 4164 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4159): Show |
chr3 | 124960710 | 125060997 | ||
a0024c0032 | 0/0 | 4143 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0025c0036 | 0/0 | 4143 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0026c0058 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0026c0059 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0027c0046 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0027c0047 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0028c0090 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0029c0075 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0030c0080 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0031c0093 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0032c0064 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0033c0072 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0034c0061 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4135): Show |
chr3 | 124960710 | 125060997 | ||
a0035c0066 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0036c0069 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0037c0050 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0038c0079 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0039c0095 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0040c0065 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0041c0051 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0042c0091 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0043c0092 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0044c0084 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0045c0073 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0046c0063 | 0/0 | 4143 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4138): Show |
chr3 | 124960710 | 125060997 | ||
a0047c0078 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0048c0094 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0049c0083 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 | ||
a0050c0070 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ATGGC others(4156): Show |
chr3 | 124960710 | 125060997 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0004 | 0/0 | 9195 | 6 | 0 | 0 | 6 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0006 | 0/0 | 9196 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0007 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0008 | 0/0 | 9197 | 7 | 0 | 1 | 6 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0010 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0011 | 0/0 | 9202 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0012 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0018 | 0/0 | 9196 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0023 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0027 | 0/0 | 9195 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0029 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0042 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0044 | 0/0 | 9203 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0045 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0047 | 0/0 | 9203 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0059 | 0/0 | 9197 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0061 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0062 | 0/0 | 9195 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0070 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0077 | 0/0 | 9202 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0092 | 0/0 | 9201 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0093 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0095 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0097 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0098 | 0/0 | 9204 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0099 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0100 | 0/0 | 9203 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0101 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0113 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0126 | 0/0 | 9197 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0001c0001t0127 | 0/0 | 9197 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0001 | 0/1 | 9201 | 13 | 0 | 3 | 5 | 0 | 4 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0005 | 0/0 | 9194 | 7 | 1 | 4 | 1 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0016 | 0/0 | 9202 | 5 | 0 | 1 | 3 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0024 | 0/0 | 9202 | 4 | 0 | 0 | 1 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0032 | 0/0 | 9201 | 3 | 0 | 0 | 0 | 0 | 3 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0033 | 0/0 | 9203 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0038 | 0/0 | 9195 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0049 | 0/0 | 9201 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0050 | 0/0 | 9201 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0051 | 0/0 | 9201 | 2 | 0 | 1 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0052 | 0/0 | 9202 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0072 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0103 | 0/0 | 9202 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0104 | 0/0 | 9201 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0105 | 0/0 | 9203 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0106 | 0/0 | 9202 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0112 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0002t0145 | 0/0 | 9203 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0010t0001 | 0/0 | 9201 | 4 | 0 | 0 | 2 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0010t0033 | 0/0 | 9203 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0010t0107 | 0/0 | 9201 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0001c0020t0012 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0001c0020t0029 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0001c0020t0041 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0001c0085t0132 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0002 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0003 | 0/0 | 9222 | 11 | 0 | 0 | 11 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0006 | 0/0 | 9214 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0007 | 0/0 | 9221 | 6 | 0 | 0 | 4 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0015 | 0/0 | 9220 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0046 | 0/0 | 9219 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9214): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0074 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0078 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0082 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0003t0089 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0004 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0009 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0010 | 0/0 | 9222 | 4 | 3 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0011 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0012 | 0/0 | 9221 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0027 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0028 | 0/0 | 9215 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0042 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0043 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0005t0135 | 0/0 | 9212 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9207): Show |
chr3 | 124960710 | 125060997 |
a0002c0014t0006 | 0/0 | 9214 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0002c0014t0015 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0002c0014t0075 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0014t0120 | 0/0 | 9214 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0002c0014t0121 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0002c0028t0020 | 0/0 | 9220 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0002c0028t0080 | 0/0 | 9222 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0033t0023 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0033t0094 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0035t0001 | 0/0 | 9219 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9214): Show |
chr3 | 124960710 | 125060997 |
a0002c0044t0023 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0048t0029 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0002c0049t0087 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0071t0083 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0002c0074t0071 | 0/0 | 9219 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9214): Show |
chr3 | 124960710 | 125060997 |
a0002c0081t0116 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0002c0082t0069 | 0/0 | 9220 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0002 | 0/0 | 9203 | 10 | 1 | 0 | 9 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0003 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0009 | 0/0 | 9203 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0014 | 0/0 | 9197 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0020 | 0/0 | 9202 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0021 | 0/0 | 9202 | 3 | 0 | 0 | 2 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0025 | 0/0 | 9197 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0039 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0040 | 0/0 | 9204 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0003c0004t0081 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0003c0034t0030 | 0/0 | 9200 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9195): Show |
chr3 | 124960710 | 125060997 |
a0003c0034t0064 | 1/0 | 9195 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0003c0045t0039 | 0/0 | 9203 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0003c0067t0019 | 0/0 | 9204 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0003c0068t0084 | 0/0 | 9203 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0013 | 0/0 | 9215 | 3 | 1 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0014 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0025 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0055 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0060 | 0/0 | 9213 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0123 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0125 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0129 | 0/0 | 9213 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0136 | 0/0 | 9212 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9207): Show |
chr3 | 124960710 | 125060997 |
a0004c0007t0137 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0038t0013 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0038t0131 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0039t0017 | 0/0 | 9213 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0040t0028 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0040t0059 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0004c0042t0004 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0042t0134 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0004c0089t0026 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0002 | 0/0 | 9203 | 3 | 0 | 1 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0003 | 0/0 | 9204 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0004 | 0/0 | 9195 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0009 | 0/0 | 9203 | 3 | 1 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0014 | 0/0 | 9197 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0019 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0022 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0054 | 0/0 | 9196 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0088 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0005c0006t0118 | 0/0 | 9196 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0005c0086t0090 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0006c0011t0010 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0006c0011t0011 | 0/0 | 9202 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0006c0011t0022 | 0/0 | 9204 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0006c0011t0086 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0006c0015t0005 | 0/0 | 9194 | 2 | 0 | 1 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0006c0015t0049 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0006c0015t0050 | 0/0 | 9201 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0006c0015t0115 | 0/0 | 9201 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9196): Show |
chr3 | 124960710 | 125060997 |
a0006c0076t0091 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0006c0077t0073 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0007c0012t0013 | 0/0 | 9212 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9207): Show |
chr3 | 124960710 | 125060997 |
a0007c0012t0017 | 0/0 | 9210 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9205): Show |
chr3 | 124960710 | 125060997 |
a0007c0013t0004 | 0/0 | 9210 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9205): Show |
chr3 | 124960710 | 125060997 |
a0007c0013t0006 | 0/0 | 9211 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9206): Show |
chr3 | 124960710 | 125060997 |
a0007c0013t0014 | 0/0 | 9212 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9207): Show |
chr3 | 124960710 | 125060997 |
a0007c0013t0058 | 0/0 | 9211 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9206): Show |
chr3 | 124960710 | 125060997 |
a0007c0013t0124 | 0/0 | 9210 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9205): Show |
chr3 | 124960710 | 125060997 |
a0007c0060t0139 | 0/0 | 9211 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9206): Show |
chr3 | 124960710 | 125060997 |
a0008c0009t0004 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0008c0009t0011 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0008c0009t0018 | 0/0 | 9196 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0008c0009t0026 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0008c0009t0061 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0008c0009t0138 | 0/0 | 9196 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0008c0027t0005 | 0/0 | 9194 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0008c0027t0140 | 0/0 | 9195 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0008c0027t0144 | 0/0 | 9194 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0009c0016t0005 | 0/0 | 9191 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9186): Show |
chr3 | 124960710 | 125060997 |
a0009c0016t0038 | 0/0 | 9192 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9187): Show |
chr3 | 124960710 | 125060997 |
a0009c0016t0141 | 0/0 | 9190 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9185): Show |
chr3 | 124960710 | 125060997 |
a0009c0016t0142 | 0/0 | 9192 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9187): Show |
chr3 | 124960710 | 125060997 |
a0009c0022t0004 | 0/0 | 9192 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9187): Show |
chr3 | 124960710 | 125060997 |
a0009c0022t0008 | 0/0 | 9194 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0009c0022t0062 | 0/0 | 9192 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9187): Show |
chr3 | 124960710 | 125060997 |
a0009c0056t0143 | 0/0 | 9191 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9186): Show |
chr3 | 124960710 | 125060997 |
a0009c0062t0014 | 0/0 | 9194 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0010c0008t0004 | 0/0 | 9195 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0010c0008t0027 | 0/0 | 9195 | 2 | 0 | 1 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0010c0008t0034 | 0/0 | 9196 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0010c0008t0036 | 0/0 | 9195 | 3 | 0 | 3 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0011c0018t0034 | 0/0 | 9196 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0011c0018t0055 | 0/0 | 9195 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0011c0018t0056 | 0/0 | 9197 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0011c0041t0035 | 0/0 | 9196 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0012c0019t0001 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0012c0019t0052 | 0/0 | 9205 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9200): Show |
chr3 | 124960710 | 125060997 |
a0012c0019t0102 | 0/0 | 9204 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0012c0019t0114 | 0/0 | 9205 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9200): Show |
chr3 | 124960710 | 125060997 |
a0012c0030t0048 | 0/0 | 9204 | 2 | 1 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0013c0017t0028 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0013c0017t0041 | 0/0 | 9220 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0013c0017t0045 | 0/0 | 9220 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0013c0017t0096 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
a0013c0087t0021 | 0/0 | 9220 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0014c0053t0001 | 0/0 | 9222 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0014c0054t0110 | 0/0 | 9222 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9217): Show |
chr3 | 124960710 | 125060997 |
a0014c0055t0002 | 0/0 | 9224 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9219): Show |
chr3 | 124960710 | 125060997 |
a0014c0097t0015 | 0/0 | 9223 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9218): Show |
chr3 | 124960710 | 125060997 |
a0015c0021t0006 | 0/0 | 9193 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9188): Show |
chr3 | 124960710 | 125060997 |
a0015c0021t0054 | 0/0 | 9193 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9188): Show |
chr3 | 124960710 | 125060997 |
a0015c0057t0128 | 0/0 | 9192 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9187): Show |
chr3 | 124960710 | 125060997 |
a0016c0025t0025 | 0/0 | 9197 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0016c0025t0130 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0017c0029t0007 | 0/0 | 9206 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9201): Show |
chr3 | 124960710 | 125060997 |
a0017c0029t0020 | 0/0 | 9205 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9200): Show |
chr3 | 124960710 | 125060997 |
a0017c0052t0020 | 0/0 | 9205 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9200): Show |
chr3 | 124960710 | 125060997 |
a0018c0037t0063 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0018c0037t0109 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0018c0088t0010 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0019c0026t0053 | 0/0 | 9194 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0019c0026t0117 | 0/0 | 9194 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0020c0043t0063 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0020c0043t0064 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0020c0096t0006 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0021c0023t0031 | 0/0 | 9202 | 3 | 3 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0022c0024t0037 | 0/0 | 9197 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0023c0031t0012 | 0/0 | 9224 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9219): Show |
chr3 | 124960710 | 125060997 |
a0023c0031t0043 | 0/0 | 9225 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9220): Show |
chr3 | 124960710 | 125060997 |
a0024c0032t0026 | 0/0 | 9196 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9191): Show |
chr3 | 124960710 | 125060997 |
a0024c0032t0065 | 0/0 | 9211 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9206): Show |
chr3 | 124960710 | 125060997 |
a0025c0036t0030 | 0/0 | 9200 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9195): Show |
chr3 | 124960710 | 125060997 |
a0026c0058t0057 | 0/0 | 9192 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9187): Show |
chr3 | 124960710 | 125060997 |
a0026c0059t0058 | 0/0 | 9193 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9188): Show |
chr3 | 124960710 | 125060997 |
a0027c0046t0019 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0027c0047t0108 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0028c0090t0119 | 0/0 | 9197 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0029c0075t0076 | 0/0 | 9204 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0030c0080t0085 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0031c0093t0014 | 0/0 | 9197 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0032c0064t0067 | 0/0 | 9211 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9206): Show |
chr3 | 124960710 | 125060997 |
a0033c0072t0026 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9209): Show |
chr3 | 124960710 | 125060997 |
a0034c0061t0035 | 0/0 | 9193 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9188): Show |
chr3 | 124960710 | 125060997 |
a0035c0066t0068 | 0/0 | 9208 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9203): Show |
chr3 | 124960710 | 125060997 |
a0036c0069t0111 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0037c0050t0022 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0038c0079t0079 | 0/0 | 9202 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9197): Show |
chr3 | 124960710 | 125060997 |
a0039c0095t0057 | 0/0 | 9195 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9190): Show |
chr3 | 124960710 | 125060997 |
a0040c0065t0066 | 0/0 | 9210 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9205): Show |
chr3 | 124960710 | 125060997 |
a0041c0051t0023 | 0/0 | 9203 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9198): Show |
chr3 | 124960710 | 125060997 |
a0042c0091t0122 | 0/0 | 9197 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9192): Show |
chr3 | 124960710 | 125060997 |
a0043c0092t0133 | 0/0 | 9213 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0044c0084t0019 | 0/0 | 9204 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9199): Show |
chr3 | 124960710 | 125060997 |
a0045c0073t0056 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9210): Show |
chr3 | 124960710 | 125060997 |
a0046c0063t0005 | 0/0 | 9194 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9189): Show |
chr3 | 124960710 | 125060997 |
a0047c0078t0015 | 0/0 | 9220 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9215): Show |
chr3 | 124960710 | 125060997 |
a0048c0094t0004 | 0/0 | 9213 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9208): Show |
chr3 | 124960710 | 125060997 |
a0049c0083t0046 | 0/0 | 9219 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9214): Show |
chr3 | 124960710 | 125060997 |
a0050c0070t0012 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | ACTCC others(9216): Show |
chr3 | 124960710 | 125060997 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0008g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0010g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0018g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0018g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0018g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0023g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0027g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0029g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0042g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0044g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0044g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0045g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0047g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0047g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0059g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0061g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0062g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0070g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0077g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0092g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0093g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0095g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0097g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0098g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0099g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0100g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0101g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0113g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0126g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0001t0127g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0016g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0016g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0016g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0016g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0024g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0024g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0024g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0024g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0032g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0032g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0033g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0033g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0038g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0038g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0049g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0050g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0051g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0051g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0052g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0072g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0103g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0104g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0105g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0106g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0112g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0002t0145g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0010t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0010t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0010t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0010t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0010t0033g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0010t0107g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0020t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0020t0029g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0020t0041g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0001c0085t0132g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0007g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0015g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0015g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0046g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0074g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0078g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0082g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0003t0089g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0010g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0012g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0027g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0028g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0028g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0042g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0043g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0005t0135g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0014t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0014t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0014t0075g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0014t0120g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0014t0121g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0028t0020g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0028t0080g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0033t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0033t0094g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0035t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0035t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0044t0023g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0048t0029g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0049t0087g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0071t0083g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0074t0071g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0081t0116g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0002c0082t0069g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0014g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0020g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0021g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0021g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0021g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0025g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0039g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0040g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0040g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0004t0081g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0034t0030g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0034t0064g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0045t0039g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0067t0019g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0003c0068t0084g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0013g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0013g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0014g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0025g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0055g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0060g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0060g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0123g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0125g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0129g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0136g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0007t0137g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0038t0013g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0038t0131g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0039t0017g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0039t0017g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0040t0028g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0040t0059g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0042t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0042t0134g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0004c0089t0026g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0009g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0014g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0019g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0022g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0054g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0088g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0006t0118g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0005c0086t0090g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0011t0010g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0011t0011g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0011t0011g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0011t0022g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0011t0086g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0015t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0015t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0015t0049g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0015t0050g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0015t0115g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0076t0091g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0006c0077t0073g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0012t0013g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0012t0013g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0012t0017g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0013t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0013t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0013t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0013t0058g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0013t0124g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0007c0060t0139g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0011g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0018g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0018g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0026g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0061g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0009t0138g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0027t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0027t0140g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0008c0027t0144g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0016t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0016t0038g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0016t0141g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0016t0142g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0022t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0022t0008g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0022t0062g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0056t0143g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0009c0062t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0027g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0027g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0034g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0036g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0036g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0010c0008t0036g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0011c0018t0034g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0011c0018t0034g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0011c0018t0055g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0011c0018t0056g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0011c0041t0035g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0011c0041t0035g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0012c0019t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0012c0019t0052g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0012c0019t0102g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0012c0019t0114g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0012c0030t0048g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0012c0030t0048g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0013c0017t0028g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0013c0017t0041g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0013c0017t0045g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0013c0017t0096g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0013c0087t0021g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0014c0053t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0014c0054t0110g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0014c0055t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0014c0097t0015g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0015c0021t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0015c0021t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0015c0021t0054g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0015c0057t0128g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0016c0025t0025g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0016c0025t0130g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0017c0029t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0017c0029t0020g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0017c0052t0020g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0018c0037t0063g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0018c0037t0109g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0018c0088t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0019c0026t0053g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0019c0026t0053g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0019c0026t0117g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0020c0043t0063g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0020c0043t0064g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0020c0096t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0021c0023t0031g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0021c0023t0031g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0021c0023t0031g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0022c0024t0037g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0022c0024t0037g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0023c0031t0012g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0023c0031t0043g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0024c0032t0026g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0024c0032t0065g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0025c0036t0030g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0025c0036t0030g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0026c0058t0057g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0026c0059t0058g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0027c0046t0019g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0027c0047t0108g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0028c0090t0119g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0029c0075t0076g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0030c0080t0085g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0031c0093t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0032c0064t0067g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0033c0072t0026g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0034c0061t0035g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0035c0066t0068g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0036c0069t0111g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0037c0050t0022g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0038c0079t0079g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0039c0095t0057g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0040c0065t0066g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0041c0051t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0042c0091t0122g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0043c0092t0133g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0044c0084t0019g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0045c0073t0056g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0046c0063t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0047c0078t0015g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0048c0094t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0049c0083t0046g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
a0050c0070t0012g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0087 | t0021 | g0091 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00099 | hp2 | a0001 | c0002 | t0051 | g0137 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00140 | hp1 | a0001 | c0002 | t0106 | g0095 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00140 | hp2 | a0003 | c0004 | t0021 | g0135 | EUR | GBR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00323 | hp1 | a0005 | c0006 | t0054 | g0247 | EUR | FIN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00323 | hp2 | a0023 | c0031 | t0012 | g0033 | EUR | FIN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00438 | hp1 | a0003 | c0004 | t0002 | g0057 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0248 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00544 | hp1 | a0006 | c0015 | t0049 | g0059 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00544 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00558 | hp1 | a0007 | c0013 | t0058 | g0228 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00558 | hp2 | a0009 | c0056 | t0143 | g0209 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00597 | hp1 | a0006 | c0015 | t0005 | g0285 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00597 | hp2 | a0004 | c0007 | t0060 | g0333 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00609 | hp1 | a0001 | c0001 | t0006 | g0280 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00609 | hp2 | a0003 | c0004 | t0003 | g0105 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00621 | hp1 | a0002 | c0048 | t0029 | g0025 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00621 | hp2 | a0002 | c0005 | t0043 | g0148 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00639 | hp1 | a0028 | c0090 | t0119 | g0348 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00639 | hp2 | a0001 | c0020 | t0029 | g0015 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00642 | hp1 | a0006 | c0011 | t0011 | g0125 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0290 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00673 | hp2 | a0002 | c0003 | t0003 | g0127 | EAS | CHS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00733 | hp1 | a0005 | c0006 | t0118 | g0295 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00733 | hp2 | a0010 | c0008 | t0027 | g0234 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00735 | hp1 | a0005 | c0006 | t0002 | g0179 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00735 | hp2 | a0016 | c0025 | t0025 | g0009 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00738 | hp1 | a0003 | c0068 | t0084 | g0197 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00738 | hp2 | a0010 | c0008 | t0036 | g0238 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00741 | hp1 | a0011 | c0018 | t0034 | g0327 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG00741 | hp2 | a0010 | c0008 | t0034 | g0233 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01071 | hp1 | a0006 | c0015 | t0005 | g0267 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01071 | hp2 | a0008 | c0009 | t0061 | g0319 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01074 | hp2 | a0016 | c0025 | t0025 | g0009 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01081 | hp1 | a0001 | c0002 | t0049 | g0055 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01081 | hp2 | a0009 | c0022 | t0008 | g0231 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01099 | hp1 | a0008 | c0009 | t0004 | g0328 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01099 | hp2 | a0001 | c0002 | t0016 | g0152 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01106 | hp1 | a0001 | c0001 | t0061 | g0288 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01106 | hp2 | a0005 | c0006 | t0009 | g0142 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01109 | hp1 | a0006 | c0011 | t0010 | g0194 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01109 | hp2 | a0002 | c0005 | t0010 | g0166 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01167 | hp1 | a0001 | c0002 | t0104 | g0180 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01167 | hp2 | a0011 | c0041 | t0035 | g0311 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01168 | hp1 | a0010 | c0008 | t0036 | g0240 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0291 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01169 | hp1 | a0010 | c0008 | t0036 | g0239 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01169 | hp2 | a0011 | c0041 | t0035 | g0309 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01192 | hp1 | a0001 | c0001 | t0127 | g0299 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01192 | hp2 | a0001 | c0085 | t0132 | g0287 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01243 | hp1 | a0004 | c0007 | t0013 | g0305 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01243 | hp2 | a0001 | c0001 | t0100 | g0096 | AMR | PUR | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01255 | hp1 | a0029 | c0075 | t0076 | g0182 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01255 | hp2 | a0013 | c0017 | t0028 | g0282 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01256 | hp1 | a0001 | c0002 | t0051 | g0138 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01256 | hp2 | a0008 | c0009 | t0138 | g0346 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0300 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01261 | hp2 | a0011 | c0018 | t0034 | g0321 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01346 | hp1 | a0004 | c0007 | t0129 | g0345 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01346 | hp2 | a0002 | c0035 | t0001 | g0155 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01358 | hp2 | a0001 | c0001 | t0044 | g0104 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01361 | hp1 | a0023 | c0031 | t0043 | g0039 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01361 | hp2 | a0008 | c0027 | t0144 | g0326 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01433 | hp1 | a0009 | c0022 | t0004 | g0230 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01433 | hp2 | a0017 | c0029 | t0007 | g0036 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01496 | hp1 | a0008 | c0027 | t0140 | g0329 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01496 | hp2 | a0004 | c0007 | t0014 | g0308 | AMR | CLM | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01517 | hp1 | a0012 | c0030 | t0048 | g0037 | EUR | IBS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01517 | hp2 | a0011 | c0018 | t0055 | g0318 | EUR | IBS | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01884 | hp1 | a0004 | c0007 | t0013 | g0312 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0082 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01891 | hp1 | a0002 | c0081 | t0116 | g0244 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01891 | hp2 | a0030 | c0080 | t0085 | g0087 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01928 | hp1 | a0007 | c0013 | t0014 | g0212 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01975 | hp1 | a0014 | c0053 | t0001 | g0034 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01975 | hp2 | a0004 | c0039 | t0017 | g0323 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01981 | hp1 | a0003 | c0004 | t0020 | g0063 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG01981 | hp2 | a0007 | c0013 | t0006 | g0227 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02004 | hp1 | a0014 | c0055 | t0002 | g0041 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02004 | hp2 | a0002 | c0003 | t0006 | g0284 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02027 | hp1 | a0003 | c0004 | t0002 | g0171 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02027 | hp2 | a0005 | c0006 | t0019 | g0111 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02055 | hp1 | a0024 | c0032 | t0065 | g0012 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02055 | hp2 | a0018 | c0037 | t0063 | g0254 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02056 | hp1 | a0001 | c0002 | t0038 | g0250 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02056 | hp2 | a0005 | c0006 | t0003 | g0112 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02074 | hp1 | a0001 | c0001 | t0099 | g0141 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02074 | hp2 | a0002 | c0003 | t0015 | g0072 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02080 | hp1 | a0002 | c0003 | t0007 | g0101 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02080 | hp2 | a0001 | c0001 | t0018 | g0252 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02083 | hp1 | a0004 | c0007 | t0136 | g0317 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02083 | hp2 | a0009 | c0016 | t0005 | g0221 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02132 | hp1 | a0031 | c0093 | t0014 | g0325 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02132 | hp2 | a0025 | c0036 | t0030 | g0068 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02135 | hp1 | a0004 | c0038 | t0131 | g0301 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02135 | hp2 | a0001 | c0002 | t0038 | g0243 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02148 | hp1 | a0001 | c0001 | t0059 | g0260 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02148 | hp2 | a0001 | c0002 | t0005 | g0253 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02155 | hp1 | a0005 | c0006 | t0014 | g0268 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02155 | hp2 | a0004 | c0007 | t0060 | g0332 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02165 | hp1 | a0001 | c0001 | t0042 | g0098 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02165 | hp2 | a0005 | c0006 | t0009 | g0048 | EAS | CDX | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02257 | hp1 | a0032 | c0064 | t0067 | g0010 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02257 | hp2 | a0019 | c0026 | t0117 | g0304 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02258 | hp1 | a0026 | c0058 | t0057 | g0219 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02258 | hp2 | a0018 | c0088 | t0010 | g0178 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02273 | hp1 | a0013 | c0017 | t0041 | g0153 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02273 | hp2 | a0001 | c0001 | t0029 | g0154 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02280 | hp1 | a0008 | c0009 | t0011 | g0203 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02280 | hp2 | a0005 | c0086 | t0090 | g0085 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0242 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02293 | hp2 | a0001 | c0010 | t0033 | g0020 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02300 | hp1 | a0014 | c0054 | t0110 | g0040 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02300 | hp2 | a0017 | c0052 | t0020 | g0042 | AMR | PEL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02451 | hp1 | a0033 | c0072 | t0026 | g0269 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02451 | hp2 | a0004 | c0007 | t0123 | g0349 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02523 | hp1 | a0002 | c0005 | t0135 | g0270 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02572 | hp1 | a0027 | c0046 | t0019 | g0024 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02572 | hp2 | a0006 | c0077 | t0073 | g0088 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02602 | hp1 | a0002 | c0028 | t0020 | g0027 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02602 | hp2 | a0001 | c0002 | t0016 | g0062 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02615 | hp1 | a0035 | c0066 | t0068 | g0011 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02615 | hp2 | a0003 | c0004 | t0014 | g0283 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02622 | hp1 | a0001 | c0020 | t0012 | g0018 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02622 | hp2 | a0004 | c0042 | t0134 | g0343 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02630 | hp1 | a0036 | c0069 | t0111 | g0202 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02630 | hp2 | a0037 | c0050 | t0022 | g0032 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02647 | hp1 | a0003 | c0004 | t0002 | g0090 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02647 | hp2 | a0038 | c0079 | t0079 | g0181 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02698 | hp1 | a0001 | c0010 | t0001 | g0031 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02698 | hp2 | a0001 | c0001 | t0126 | g0272 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02717 | hp1 | a0004 | c0007 | t0055 | g0320 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02717 | hp2 | a0027 | c0047 | t0108 | g0017 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02723 | hp1 | a0011 | c0018 | t0056 | g0350 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02723 | hp2 | a0024 | c0032 | t0026 | g0241 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02735 | hp1 | a0001 | c0002 | t0024 | g0139 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02735 | hp2 | a0003 | c0045 | t0039 | g0028 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02738 | hp1 | a0001 | c0001 | t0098 | g0189 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02738 | hp2 | a0001 | c0001 | t0077 | g0044 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02809 | hp1 | a0002 | c0003 | t0082 | g0185 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02809 | hp2 | a0007 | c0060 | t0139 | g0217 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02818 | hp1 | a0026 | c0059 | t0058 | g0220 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02818 | hp2 | a0039 | c0095 | t0057 | g0315 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02886 | hp1 | a0016 | c0025 | t0130 | g0316 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02886 | hp2 | a0002 | c0005 | t0010 | g0067 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02895 | hp1 | a0040 | c0065 | t0066 | g0013 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02895 | hp2 | a0002 | c0005 | t0010 | g0045 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02965 | hp1 | a0006 | c0011 | t0022 | g0003 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02965 | hp2 | a0041 | c0051 | t0023 | g0022 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02970 | hp1 | a0001 | c0020 | t0041 | g0019 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02970 | hp2 | a0042 | c0091 | t0122 | g0310 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03041 | hp1 | a0020 | c0043 | t0063 | g0340 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03041 | hp2 | a0001 | c0001 | t0092 | g0188 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03098 | hp1 | a0021 | c0023 | t0031 | g0191 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03098 | hp2 | a0005 | c0006 | t0022 | g0089 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03139 | hp1 | a0006 | c0011 | t0022 | g0003 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03139 | hp2 | a0043 | c0092 | t0133 | g0314 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03195 | hp1 | a0003 | c0004 | t0081 | g0177 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03195 | hp2 | a0002 | c0033 | t0023 | g0164 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03209 | hp1 | a0021 | c0023 | t0031 | g0190 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03209 | hp2 | a0004 | c0042 | t0004 | g0347 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03239 | hp2 | a0003 | c0034 | t0030 | g0115 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03453 | hp1 | a0002 | c0082 | t0069 | g0193 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03486 | hp1 | a0008 | c0009 | t0026 | g0342 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03486 | hp2 | a0006 | c0011 | t0086 | g0081 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03490 | hp1 | a0001 | c0002 | t0032 | g0007 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03490 | hp2 | a0001 | c0002 | t0005 | g0298 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03491 | hp1 | a0010 | c0008 | t0027 | g0235 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03491 | hp2 | a0001 | c0002 | t0024 | g0093 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03492 | hp1 | a0001 | c0002 | t0024 | g0094 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03492 | hp2 | a0001 | c0002 | t0032 | g0007 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03516 | hp1 | a0021 | c0023 | t0031 | g0183 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03516 | hp2 | a0003 | c0004 | t0040 | g0175 | AFR | ESN | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03540 | hp1 | a0004 | c0007 | t0025 | g0307 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03540 | hp2 | a0020 | c0043 | t0064 | g0339 | AFR | GWD | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03579 | hp1 | a0045 | c0073 | t0056 | g0297 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03579 | hp2 | a0003 | c0004 | t0040 | g0176 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03654 | hp1 | a0005 | c0006 | t0004 | g0289 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03654 | hp2 | a0002 | c0003 | t0007 | g0083 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03710 | hp1 | a0001 | c0002 | t0103 | g0160 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03710 | hp2 | a0046 | c0063 | t0005 | g0237 | SAS | PJL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03831 | hp1 | a0003 | c0067 | t0019 | g0064 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03831 | hp2 | a0002 | c0003 | t0006 | g0265 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03834 | hp1 | a0001 | c0002 | t0032 | g0200 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03834 | hp2 | a0010 | c0008 | t0004 | g0236 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03927 | hp1 | a0006 | c0015 | t0050 | g0065 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03927 | hp2 | a0047 | c0078 | t0015 | g0156 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04115 | hp1 | a0001 | c0010 | t0001 | g0026 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04115 | hp2 | a0001 | c0001 | t0044 | g0161 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04184 | hp2 | a0006 | c0011 | t0011 | g0061 | SAS | BEB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04199 | hp1 | a0001 | c0002 | t0145 | g0351 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04199 | hp2 | a0002 | c0028 | t0080 | g0029 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04228 | hp1 | a0001 | c0010 | t0107 | g0021 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG04228 | hp2 | a0002 | c0003 | t0007 | g0149 | SAS | STU | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18612 | hp1 | a0001 | c0002 | t0016 | g0146 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18612 | hp2 | a0008 | c0009 | t0018 | g0337 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18747 | hp1 | a0002 | c0005 | t0012 | g0158 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18747 | hp2 | a0001 | c0002 | t0005 | g0286 | EAS | CHB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18906 | hp1 | a0002 | c0044 | t0023 | g0016 | AFR | YRI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18906 | hp2 | a0001 | c0001 | t0070 | g0195 | AFR | YRI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18939 | hp1 | a0001 | c0001 | t0018 | g0251 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18939 | hp2 | a0013 | c0017 | t0045 | g0132 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18940 | hp1 | a0001 | c0001 | t0010 | g0069 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18940 | hp2 | a0007 | c0012 | t0017 | g0002 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18941 | hp1 | a0001 | c0001 | t0045 | g0129 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0246 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18942 | hp1 | a0001 | c0001 | t0047 | g0124 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18944 | hp1 | a0022 | c0024 | t0037 | g0008 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18944 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18945 | hp1 | a0003 | c0004 | t0021 | g0058 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18945 | hp2 | a0005 | c0006 | t0002 | g0099 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18946 | hp1 | a0002 | c0003 | t0015 | g0084 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18946 | hp2 | a0001 | c0001 | t0008 | g0292 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18948 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18948 | hp2 | a0001 | c0010 | t0001 | g0014 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18950 | hp1 | a0008 | c0027 | t0005 | g0331 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18950 | hp2 | a0002 | c0003 | t0007 | g0071 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18951 | hp1 | a0002 | c0005 | t0011 | g0198 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18951 | hp2 | a0003 | c0004 | t0009 | g0196 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18952 | hp1 | a0048 | c0094 | t0004 | g0330 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18952 | hp2 | a0002 | c0003 | t0007 | g0070 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18953 | hp1 | a0025 | c0036 | t0030 | g0120 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18953 | hp2 | a0001 | c0001 | t0027 | g0279 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18957 | hp1 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18959 | hp1 | a0006 | c0015 | t0115 | g0056 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18959 | hp2 | a0001 | c0001 | t0012 | g0173 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18960 | hp1 | a0004 | c0007 | t0137 | g0335 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18966 | hp1 | a0012 | c0019 | t0114 | g0204 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18967 | hp2 | a0003 | c0004 | t0002 | g0168 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18968 | hp1 | a0002 | c0014 | t0015 | g0117 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18968 | hp2 | a0001 | c0002 | t0112 | g0150 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18970 | hp1 | a0009 | c0016 | t0038 | g0218 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18970 | hp2 | a0002 | c0005 | t0004 | g0276 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18973 | hp1 | a0004 | c0007 | t0013 | g0336 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18973 | hp2 | a0022 | c0024 | t0037 | g0008 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18974 | hp1 | a0003 | c0004 | t0009 | g0050 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18974 | hp2 | a0002 | c0003 | t0089 | g0126 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18975 | hp1 | a0001 | c0002 | t0052 | g0136 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18975 | hp2 | a0002 | c0003 | t0003 | g0107 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18977 | hp1 | a0002 | c0035 | t0001 | g0103 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18977 | hp2 | a0001 | c0001 | t0062 | g0278 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18982 | hp1 | a0003 | c0004 | t0002 | g0170 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18983 | hp1 | a0001 | c0001 | t0113 | g0151 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18983 | hp2 | a0002 | c0003 | t0002 | g0157 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18986 | hp1 | a0022 | c0024 | t0037 | g0263 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18986 | hp2 | a0009 | c0062 | t0014 | g0213 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18988 | hp1 | a0014 | c0097 | t0015 | g0206 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18988 | hp2 | a0003 | c0004 | t0009 | g0073 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18989 | hp1 | a0001 | c0002 | t0033 | g0051 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18990 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18990 | hp2 | a0002 | c0003 | t0078 | g0074 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18991 | hp1 | a0049 | c0083 | t0046 | g0119 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18991 | hp2 | a0007 | c0013 | t0124 | g0232 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18993 | hp1 | a0012 | c0019 | t0052 | g0207 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18993 | hp2 | a0002 | c0074 | t0071 | g0192 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18994 | hp1 | a0002 | c0003 | t0003 | g0100 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18994 | hp2 | a0001 | c0001 | t0095 | g0102 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18995 | hp2 | a0002 | c0003 | t0003 | g0174 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18997 | hp1 | a0002 | c0049 | t0087 | g0030 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18997 | hp2 | a0004 | c0038 | t0013 | g0322 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18998 | hp1 | a0015 | c0021 | t0006 | g0215 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18998 | hp2 | a0008 | c0009 | t0018 | g0324 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18999 | hp1 | a0007 | c0012 | t0013 | g0226 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18999 | hp2 | a0002 | c0005 | t0028 | g0257 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19000 | hp1 | a0015 | c0021 | t0054 | g0214 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19000 | hp2 | a0001 | c0002 | t0016 | g0047 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19001 | hp1 | a0004 | c0040 | t0028 | g0334 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19001 | hp2 | a0003 | c0004 | t0002 | g0167 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19002 | hp1 | a0009 | c0016 | t0142 | g0224 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19002 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19003 | hp1 | a0001 | c0001 | t0008 | g0245 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19003 | hp2 | a0004 | c0039 | t0017 | g0338 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0266 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19009 | hp2 | a0007 | c0012 | t0013 | g0225 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19010 | hp2 | a0002 | c0003 | t0046 | g0118 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19012 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19012 | hp2 | a0002 | c0014 | t0121 | g0255 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19030 | hp1 | a0020 | c0096 | t0006 | g0341 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19030 | hp2 | a0004 | c0089 | t0026 | g0306 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19043 | hp1 | a0002 | c0071 | t0083 | g0186 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19043 | hp2 | a0015 | c0057 | t0128 | g0210 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19054 | hp1 | a0002 | c0003 | t0074 | g0076 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19054 | hp2 | a0009 | c0022 | t0062 | g0229 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19055 | hp1 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19055 | hp2 | a0007 | c0012 | t0017 | g0002 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19056 | hp1 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19056 | hp2 | a0001 | c0001 | t0101 | g0122 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19057 | hp1 | a0007 | c0012 | t0017 | g0002 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19057 | hp2 | a0001 | c0002 | t0016 | g0052 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19060 | hp1 | a0050 | c0070 | t0012 | g0053 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19060 | hp2 | a0012 | c0019 | t0001 | g0208 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19062 | hp1 | a0002 | c0005 | t0028 | g0259 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19062 | hp2 | a0015 | c0021 | t0006 | g0216 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19063 | hp1 | a0001 | c0001 | t0018 | g0249 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19063 | hp2 | a0003 | c0004 | t0002 | g0172 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19064 | hp1 | a0001 | c0001 | t0008 | g0264 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19064 | hp2 | a0001 | c0002 | t0072 | g0134 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19067 | hp1 | a0002 | c0014 | t0006 | g0256 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19067 | hp2 | a0012 | c0019 | t0102 | g0205 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19068 | hp1 | a0002 | c0014 | t0120 | g0261 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19068 | hp2 | a0002 | c0005 | t0042 | g0159 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19070 | hp1 | a0003 | c0004 | t0025 | g0271 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19070 | hp2 | a0001 | c0010 | t0001 | g0023 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19076 | hp1 | a0001 | c0002 | t0024 | g0116 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19078 | hp1 | a0005 | c0006 | t0003 | g0110 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19078 | hp2 | a0013 | c0017 | t0096 | g0049 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19079 | hp1 | a0001 | c0002 | t0033 | g0046 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19079 | hp2 | a0001 | c0001 | t0047 | g0123 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19082 | hp1 | a0002 | c0005 | t0027 | g0258 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19082 | hp2 | a0001 | c0002 | t0105 | g0140 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19084 | hp1 | a0002 | c0014 | t0075 | g0079 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19084 | hp2 | a0003 | c0004 | t0021 | g0169 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19086 | hp1 | a0002 | c0003 | t0003 | g0106 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19086 | hp2 | a0001 | c0001 | t0097 | g0145 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19088 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19088 | hp2 | a0002 | c0005 | t0012 | g0113 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19090 | hp1 | a0002 | c0003 | t0007 | g0077 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19090 | hp2 | a0007 | c0013 | t0004 | g0211 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19091 | hp1 | a0001 | c0001 | t0023 | g0060 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA19091 | hp2 | a0005 | c0006 | t0002 | g0109 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA20129 | hp1 | a0005 | c0006 | t0088 | g0066 | AFR | ASW | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA20129 | hp2 | a0001 | c0001 | t0093 | g0163 | AFR | ASW | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA20752 | hp1 | a0001 | c0002 | t0050 | g0199 | EUR | TSI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA20752 | hp2 | a0017 | c0029 | t0020 | g0035 | EUR | TSI | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02109 | hp1 | a0018 | c0037 | t0109 | g0187 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02109 | hp2 | a0019 | c0026 | t0053 | g0303 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02486 | hp1 | a0004 | c0040 | t0059 | g0313 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02486 | hp2 | a0034 | c0061 | t0035 | g0222 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02559 | hp1 | a0001 | c0002 | t0005 | g0296 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG02559 | hp2 | a0004 | c0007 | t0125 | g0344 | AFR | ACB | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03471 | hp1 | a0019 | c0026 | t0053 | g0302 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG03471 | hp2 | a0044 | c0084 | t0019 | g0086 | AFR | MSL | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG06807 | hp1 | a0012 | c0030 | t0048 | g0038 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
HG06807 | hp2 | a0002 | c0033 | t0094 | g0165 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18955 | hp1 | a0002 | c0005 | t0009 | g0078 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA18955 | hp2 | a0009 | c0016 | t0141 | g0223 | EAS | JPT | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA20300 | hp1 | a0002 | c0005 | t0010 | g0201 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA20300 | hp2 | a0005 | c0006 | t0009 | g0043 | AFR | USA | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA21309 | hp1 | a0006 | c0076 | t0091 | g0162 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
NA21309 | hp2 | a0003 | c0004 | t0039 | g0054 | AFR | LWK | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0128 | REF | REF | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
homoSapiens | grch38p0 | a0003 | c0034 | t0064 | g0262 | REF | REF | HEG1_chr3_124960710_125060997 | HEG1 | chr3 | 124960710 | 125060997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:124970801 | G | T | 1 | a0045 | 1 | HG03579.hp1 | missense_variant&splice_region_variant | MODERATE | c.3997C>A | p.Pro1333Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4104/9195 | 3997/4146 | 1333/1381 | chr3 | 124970801 | |||
chr3:124973819 | C | T | 1 | a0036 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.3908G>A | p.Arg1303His | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/17 | 4015/9195 | 3908/4146 | 1303/1381 | chr3 | 124973819 | |||
chr3:124997805 | C | T | 1 | a0042 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3536G>A | p.Arg1179Gln | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/17 | 3643/9195 | 3536/4146 | 1179/1381 | chr3 | 124997805 | |||
chr3:125005330 | A | C | 1 | a0037 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.3232T>G | p.Phe1078Val | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/17 | 3339/9195 | 3232/4146 | 1078/1381 | chr3 | 125005330 | |||
chr3:125009743 | G | A | 1 | a0002 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.3155C>T | p.Pro1052Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/17 | 3262/9195 | 3155/4146 | 1052/1381 | chr3 | 125009743 | |||
chr3:125009782 | A | G | 28 | a0001 a0002 a0004 others(25): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
missense_variant | MODERATE | c.3116T>C | p.Met1039Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/17 | 3223/9195 | 3116/4146 | 1039/1381 | chr3 | 125009782 | |||
chr3:125012641 | C | G | 34 | a0001 a0002 a0004 others(31): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
missense_variant | MODERATE | c.2938G>C | p.Val980Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 3045/9195 | 2938/4146 | 980/1381 | chr3 | 125012641 | |||
chr3:125012709 | G | A | 4 | a0026 a0027 a0035 others(1): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.2870C>T | p.Thr957Met | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2977/9195 | 2870/4146 | 957/1381 | chr3 | 125012709 | |||
chr3:125012845 | T | A | 17 | a0002 a0004 a0007 others(14): Show |
119 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(116): Show |
missense_variant | MODERATE | c.2734A>T | p.Thr912Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2841/9195 | 2734/4146 | 912/1381 | chr3 | 125012845 | |||
chr3:125012956 | T | A | 1 | a0025 | 2 | HG02132.hp2 NA18953.hp1 |
missense_variant | MODERATE | c.2623A>T | p.Thr875Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2730/9195 | 2623/4146 | 875/1381 | chr3 | 125012956 | |||
chr3:125013258 | T | C | 3 | a0016 a0028 a0029 |
5 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
missense_variant | MODERATE | c.2321A>G | p.Gln774Arg | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2428/9195 | 2321/4146 | 774/1381 | chr3 | 125013258 | |||
chr3:125013351 | G | A | 1 | a0021 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.2228C>T | p.Ser743Phe | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2335/9195 | 2228/4146 | 743/1381 | chr3 | 125013351 | |||
chr3:125013490 | C | T | 3 | a0016 a0028 a0029 |
5 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
missense_variant | MODERATE | c.2089G>A | p.Ala697Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2196/9195 | 2089/4146 | 697/1381 | chr3 | 125013490 | |||
chr3:125013575 | A | AGAGGAGG others(11): Show |
13 | a0002 a0004 a0007 others(10): Show |
111 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(108): Show |
disruptive_inframe_insertion | MODERATE | c.1986_2003dupCTCTTC others(12): Show |
p.Ser663_Ser668dup | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2110/9195 | 2003/4146 | 668/1381 | chr3 | 125013575 | |||
chr3:125013582 | G | A | 6 | a0021 a0026 a0027 others(3): Show |
10 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
missense_variant | MODERATE | c.1997C>T | p.Ser666Phe | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2104/9195 | 1997/4146 | 666/1381 | chr3 | 125013582 | |||
chr3:125013651 | G | A | 1 | a0016 | 3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1928C>T | p.Pro643Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2035/9195 | 1928/4146 | 643/1381 | chr3 | 125013651 | |||
chr3:125013774 | A | G | 14 | a0001 a0005 a0008 others(11): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(156): Show |
missense_variant | MODERATE | c.1805T>C | p.Phe602Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 1912/9195 | 1805/4146 | 602/1381 | chr3 | 125013774 | |||
chr3:125013895 | T | A | 4 | a0026 a0027 a0035 others(1): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.1684A>T | p.Thr562Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 1791/9195 | 1684/4146 | 562/1381 | chr3 | 125013895 | |||
chr3:125013976 | A | G | 1 | a0022 | 3 | NA18944.hp1 NA18973.hp2 NA18986.hp1 |
missense_variant | MODERATE | c.1603T>C | p.Tyr535His | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 1710/9195 | 1603/4146 | 535/1381 | chr3 | 125013976 | |||
chr3:125019409 | T | C | 1 | a0047 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1441A>G | p.Asn481Asp | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/17 | 1548/9195 | 1441/4146 | 481/1381 | chr3 | 125019409 | |||
chr3:125027205 | A | G | 21 | a0001 a0005 a0008 others(18): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
missense_variant&splice_region_variant | MODERATE | c.913T>C | p.Ser305Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 1020/9195 | 913/4146 | 305/1381 | chr3 | 125027205 | |||
chr3:125027397 | C | G | 1 | a0021 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.721G>C | p.Gly241Arg | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 828/9195 | 721/4146 | 241/1381 | chr3 | 125027397 | |||
chr3:125027504 | G | A | 1 | a0049 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.614C>T | p.Ser205Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 721/9195 | 614/4146 | 205/1381 | chr3 | 125027504 | |||
chr3:125029285 | C | T | 2 | a0037 a0041 |
2 | HG02630.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.520G>A | p.Gly174Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/17 | 627/9195 | 520/4146 | 174/1381 | chr3 | 125029285 | |||
chr3:125055588 | T | G | 14 | a0004 a0008 a0010 others(11): Show |
61 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
missense_variant | MODERATE | c.303A>C | p.Arg101Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 410/9195 | 303/4146 | 101/1381 | chr3 | 125055588 | |||
chr3:125055718 | C | T | 4 | a0024 a0032 a0035 others(1): Show |
5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
missense_variant | MODERATE | c.173G>A | p.Arg58His | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 280/9195 | 173/4146 | 58/1381 | chr3 | 125055718 | |||
chr3:125055799 | C | T | 2 | a0010 a0046 |
8 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
missense_variant | MODERATE | c.92G>A | p.Arg31Gln | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 199/9195 | 92/4146 | 31/1381 | chr3 | 125055799 | |||
chr3:125055810 | GGCC | G | 5 | a0007 a0009 a0015 others(2): Show |
27 | HG00558.hp1 HG00558.hp2 HG01081.hp2 others(24): Show |
disruptive_inframe_deletion | MODERATE | c.78_80delGGC | p.Ala27del | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 187/9195 | 78/4146 | 26/1381 | chr3 | 125055810 | |||
chr3:125055820 | G | GGCA | 2 | a0012 a0014 |
5 | NA18966.hp1 NA18988.hp1 NA18993.hp1 others(2): Show |
conservative_inframe_insertion | MODERATE | c.68_70dupTGC | p.Leu23dup | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 177/9195 | 70/4146 | 24/1381 | chr3 | 125055820 | |||
chr3:125055821 | G | GCAT | 4 | a0012 a0014 a0017 others(1): Show |
10 | HG00323.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
conservative_inframe_insertion | MODERATE | c.69_70insATG | p.Leu23_Pro24insMet | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 176/9195 | 69/4146 | 23/1381 | chr3 | 125055821 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:124970766 | G | A | 1 | a0002c0082 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.4032C>T | p.Asn1344Asn | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4139/9195 | 4032/4146 | 1344/1381 | chr3 | 124970766 | |||
chr3:124973845 | C | T | 73 | a0001c0001 a0001c0020 a0001c0085 others(70): Show |
266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
synonymous_variant | LOW | c.3882G>A | p.Pro1294Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/17 | 3989/9195 | 3882/4146 | 1294/1381 | chr3 | 124973845 | |||
chr3:124977894 | G | A | 1 | a0002c0048 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.3786C>T | p.Leu1262Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/17 | 3893/9195 | 3786/4146 | 1262/1381 | chr3 | 124977894 | |||
chr3:125001880 | G | A | 1 | a0003c0067 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.3489C>T | p.Leu1163Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/17 | 3596/9195 | 3489/4146 | 1163/1381 | chr3 | 125001880 | |||
chr3:125009742 | C | T | 3 | a0014c0053 a0028c0090 a0029c0075 |
3 | HG00639.hp1 HG01255.hp1 HG01975.hp1 |
synonymous_variant | LOW | c.3156G>A | p.Pro1052Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/17 | 3263/9195 | 3156/4146 | 1052/1381 | chr3 | 125009742 | |||
chr3:125012933 | C | T | 1 | a0006c0076 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2646G>A | p.Ser882Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2753/9195 | 2646/4146 | 882/1381 | chr3 | 125012933 | |||
chr3:125013254 | A | G | 1 | a0001c0085 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.2325T>C | p.Thr775Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2432/9195 | 2325/4146 | 775/1381 | chr3 | 125013254 | |||
chr3:125013650 | C | T | 1 | a0002c0071 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1929G>A | p.Pro643Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/17 | 2036/9195 | 1929/4146 | 643/1381 | chr3 | 125013650 | |||
chr3:125019263 | C | T | 37 | a0001c0001 a0001c0002 a0001c0010 others(34): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
splice_region_variant&synonymous_variant | LOW | c.1587G>A | p.Ser529Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/17 | 1694/9195 | 1587/4146 | 529/1381 | chr3 | 125019263 | |||
chr3:125021003 | C | T | 1 | a0038c0079 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1041G>A | p.Thr347Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/17 | 1148/9195 | 1041/4146 | 347/1381 | chr3 | 125021003 | |||
chr3:125021048 | G | A | 45 | a0001c0001 a0001c0002 a0001c0010 others(42): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
synonymous_variant | LOW | c.996C>T | p.Ala332Ala | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/17 | 1103/9195 | 996/4146 | 332/1381 | chr3 | 125021048 | |||
chr3:125027302 | G | A | 1 | a0017c0052 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.816C>T | p.Thr272Thr | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 923/9195 | 816/4146 | 272/1381 | chr3 | 125027302 | |||
chr3:125027338 | C | A | 40 | a0001c0001 a0001c0002 a0001c0010 others(37): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
synonymous_variant | LOW | c.780G>T | p.Pro260Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 887/9195 | 780/4146 | 260/1381 | chr3 | 125027338 | |||
chr3:125027338 | C | T | 6 | a0026c0058 a0026c0059 a0027c0046 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.780G>A | p.Pro260Pro | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 887/9195 | 780/4146 | 260/1381 | chr3 | 125027338 | |||
chr3:125027395 | C | T | 1 | a0004c0038 | 2 | HG02135.hp1 NA18997.hp2 |
synonymous_variant | LOW | c.723G>A | p.Gly241Gly | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 830/9195 | 723/4146 | 241/1381 | chr3 | 125027395 | |||
chr3:125027452 | G | A | 1 | a0003c0068 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.666C>T | p.Ala222Ala | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 773/9195 | 666/4146 | 222/1381 | chr3 | 125027452 | |||
chr3:125027503 | T | C | 74 | a0001c0001 a0001c0002 a0001c0010 others(71): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
synonymous_variant | LOW | c.615A>G | p.Ser205Ser | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/17 | 722/9195 | 615/4146 | 205/1381 | chr3 | 125027503 | |||
chr3:125029382 | G | A | 34 | a0001c0001 a0001c0002 a0001c0010 others(31): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
synonymous_variant | LOW | c.423C>T | p.Gly141Gly | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/17 | 530/9195 | 423/4146 | 141/1381 | chr3 | 125029382 | |||
chr3:125055741 | C | T | 1 | a0009c0056 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.150G>A | p.Ala50Ala | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 257/9195 | 150/4146 | 50/1381 | chr3 | 125055741 | |||
chr3:125055828 | C | T | 11 | a0001c0010 a0001c0020 a0002c0028 others(8): Show |
19 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(16): Show |
synonymous_variant | LOW | c.63G>A | p.Leu21Leu | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 170/9195 | 63/4146 | 21/1381 | chr3 | 125055828 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:124965817 | T | C | 1 | a0015c0057t0128 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4835A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4835 | chr3 | 124965817 | ||||||
chr3:124966122 | C | T | 240 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(237): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*4530G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4530 | chr3 | 124966122 | ||||||
chr3:124966290 | G | T | 1 | a0021c0023t0031 | 3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4362C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4362 | chr3 | 124966290 | ||||||
chr3:124966385 | T | C | 2 | a0002c0033t0094 a0029c0075t0076 |
2 | HG01255.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4267A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4267 | chr3 | 124966385 | ||||||
chr3:124966565 | C | T | 2 | a0001c0001t0126 a0043c0092t0133 |
2 | HG02698.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4087G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 4087 | chr3 | 124966565 | ||||||
chr3:124966653 | T | C | 1 | a0004c0007t0129 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3999A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3999 | chr3 | 124966653 | ||||||
chr3:124966728 | T | C | 13 | a0001c0002t0049 a0002c0081t0116 a0003c0004t0040 others(10): Show |
15 | HG00544.hp1 HG00639.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3924A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3924 | chr3 | 124966728 | ||||||
chr3:124967032 | A | T | 2 | a0002c0081t0116 a0002c0082t0069 |
2 | HG01891.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3620T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3620 | chr3 | 124967032 | ||||||
chr3:124967124 | T | C | 1 | a0006c0076t0091 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3528A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3528 | chr3 | 124967124 | ||||||
chr3:124967333 | C | T | 1 | a0001c0010t0107 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3319G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3319 | chr3 | 124967333 | ||||||
chr3:124967387 | T | C | 2 | a0001c0001t0095 a0002c0014t0121 |
2 | NA18994.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3265A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3265 | chr3 | 124967387 | ||||||
chr3:124967413 | T | C | 13 | a0001c0001t0100 a0001c0002t0032 a0001c0002t0050 others(10): Show |
18 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3239A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3239 | chr3 | 124967413 | ||||||
chr3:124967457 | A | AT | 71 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0029 others(68): Show |
101 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3194dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3194 | chr3 | 124967457 | ||||||
chr3:124967457 | AT | A | 89 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0027 others(86): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*3194delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3194 | chr3 | 124967457 | ||||||
chr3:124967457 | ATT | A | 9 | a0001c0001t0092 a0002c0003t0046 a0002c0005t0135 others(6): Show |
10 | HG02083.hp1 HG02132.hp2 HG02523.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3193_*3194delAA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3193 | chr3 | 124967457 | ||||||
chr3:124967486 | G | A | 1 | a0004c0007t0123 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3166C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 3166 | chr3 | 124967486 | ||||||
chr3:124967663 | A | G | 208 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(205): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*2989T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2989 | chr3 | 124967663 | ||||||
chr3:124967729 | G | C | 1 | a0014c0054t0110 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2923C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2923 | chr3 | 124967729 | ||||||
chr3:124967889 | C | A | 94 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(91): Show |
153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2763G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2763 | chr3 | 124967889 | ||||||
chr3:124968100 | C | T | 3 | a0006c0077t0073 a0015c0057t0128 a0024c0032t0065 |
3 | HG02055.hp1 HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2552G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2552 | chr3 | 124968100 | ||||||
chr3:124968125 | G | C | 1 | a0002c0081t0116 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2527C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2527 | chr3 | 124968125 | ||||||
chr3:124968190 | T | C | 1 | a0003c0068t0084 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2462A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2462 | chr3 | 124968190 | ||||||
chr3:124968211 | C | T | 2 | a0002c0081t0116 a0002c0082t0069 |
2 | HG01891.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2441G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2441 | chr3 | 124968211 | ||||||
chr3:124968245 | C | T | 2 | a0001c0001t0126 a0001c0001t0127 |
2 | HG01192.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2407G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2407 | chr3 | 124968245 | ||||||
chr3:124968248 | C | T | 2 | a0002c0081t0116 a0002c0082t0069 |
2 | HG01891.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2404G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2404 | chr3 | 124968248 | ||||||
chr3:124968550 | G | C | 1 | a0005c0006t0088 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2102 | chr3 | 124968550 | ||||||
chr3:124968588 | G | A | 17 | a0001c0001t0044 a0001c0001t0045 a0001c0001t0061 others(14): Show |
19 | HG00597.hp2 HG01071.hp2 HG01106.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2064C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2064 | chr3 | 124968588 | ||||||
chr3:124968616 | C | T | 60 | a0001c0001t0006 a0001c0002t0103 a0002c0003t0002 others(57): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*2036G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2036 | chr3 | 124968616 | ||||||
chr3:124968617 | G | A | 1 | a0001c0002t0051 | 2 | HG00099.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 2035 | chr3 | 124968617 | ||||||
chr3:124968677 | C | T | 1 | a0001c0085t0132 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1975 | chr3 | 124968677 | ||||||
chr3:124968711 | C | T | 4 | a0001c0002t0104 a0008c0027t0140 a0008c0027t0144 others(1): Show |
5 | HG01167.hp1 HG01361.hp2 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1941G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1941 | chr3 | 124968711 | ||||||
chr3:124968803 | G | A | 1 | a0002c0003t0089 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1849C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1849 | chr3 | 124968803 | ||||||
chr3:124968923 | G | T | 183 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(180): Show |
257 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*1729C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1729 | chr3 | 124968923 | ||||||
chr3:124969072 | G | A | 1 | a0008c0027t0144 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1580C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1580 | chr3 | 124969072 | ||||||
chr3:124969093 | G | T | 1 | a0012c0019t0102 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1559C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1559 | chr3 | 124969093 | ||||||
chr3:124969425 | T | C | 87 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(84): Show |
116 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1227A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1227 | chr3 | 124969425 | ||||||
chr3:124969572 | C | T | 22 | a0001c0001t0007 a0002c0003t0007 a0002c0003t0015 others(19): Show |
34 | HG00639.hp1 HG00733.hp1 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1080G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 1080 | chr3 | 124969572 | ||||||
chr3:124969770 | T | A | 1 | a0007c0060t0139 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 882 | chr3 | 124969770 | ||||||
chr3:124969795 | C | CA | 190 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(187): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*857insT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 856 | chr3 | 124969795 | ||||||
chr3:124969947 | A | T | 187 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(184): Show |
264 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*705T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 705 | chr3 | 124969947 | ||||||
chr3:124970157 | C | T | 22 | a0001c0001t0007 a0001c0001t0077 a0002c0003t0007 others(19): Show |
34 | HG00639.hp1 HG00733.hp1 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*495G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 495 | chr3 | 124970157 | ||||||
chr3:124970158 | G | A | 1 | a0001c0001t0113 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 494 | chr3 | 124970158 | ||||||
chr3:124970243 | A | G | 1 | a0001c0002t0072 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 409 | chr3 | 124970243 | ||||||
chr3:124970371 | C | T | 1 | a0001c0002t0145 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*281G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 281 | chr3 | 124970371 | ||||||
chr3:124970372 | G | A | 1 | a0012c0019t0114 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 280 | chr3 | 124970372 | ||||||
chr3:124970513 | C | G | 1 | a0002c0074t0071 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 139 | chr3 | 124970513 | ||||||
chr3:124970559 | C | T | 5 | a0001c0001t0070 a0002c0081t0116 a0002c0082t0069 others(2): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*93G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 93 | chr3 | 124970559 | ||||||
chr3:124970612 | G | C | 1 | a0006c0015t0115 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 17/17 | 40 | chr3 | 124970612 | ||||||
chr3:125055935 | A | AGGGCAGC | 134 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0011 others(131): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
5_prime_UTR_variant | MODIFIER | c.-52_-46dupGCTGCCC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 46 | chr3 | 125055935 | ||||||
chr3:125055935 | A | AGGGCAGC others(7): Show |
4 | a0024c0032t0065 a0032c0064t0067 a0035c0066t0068 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-59_-46dupGCTGCCCG others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 46 | chr3 | 125055935 | ||||||
chr3:125055976 | G | A | 1 | a0001c0002t0145 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/17 | 86 | chr3 | 125055976 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:124971268 | A | G | 7 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 others(4): Show |
7 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.3997-467T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971268 | |||||||
chr3:124971450 | C | CT | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
164 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.3997-650dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971450 | |||||||
chr3:124971478 | CTTTTCTT others(4): Show |
C | 2 | a0035c0066t0068g0011 a0036c0069t0111g0202 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3997-688_3997-678d others(13): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971478 | |||||||
chr3:124971680 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3997-879G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971680 | |||||||
chr3:124971789 | C | CT | 84 | a0001c0001t0070g0195 a0001c0002t0001g0144 a0001c0002t0016g0047 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3997-989dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971789 | |||||||
chr3:124971789 | C | CTT | 157 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(154): Show |
162 | HG00323.hp2 HG00597.hp2 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.3997-990_3997-989d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971789 | |||||||
chr3:124971789 | C | CTTT | 23 | a0001c0001t0007g0114 a0001c0001t0008g0248 a0001c0001t0059g0260 others(20): Show |
25 | HG00438.hp2 HG00735.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.3997-991_3997-989d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124971789 | |||||||
chr3:124972148 | C | T | 1 | a0004c0040t0059g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3997-1347G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972148 | |||||||
chr3:124972351 | T | C | 1 | a0044c0084t0019g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3996+1380A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972351 | |||||||
chr3:124972366 | A | C | 3 | a0001c0002t0005g0253 a0001c0002t0005g0290 a0001c0002t0005g0291 |
3 | HG00642.hp2 HG01168.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.3996+1365T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972366 | |||||||
chr3:124972437 | T | C | 1 | a0026c0058t0057g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3996+1294A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972437 | |||||||
chr3:124972480 | A | G | 1 | a0001c0002t0016g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3996+1251T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972480 | |||||||
chr3:124972626 | T | C | 259 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(256): Show |
269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3996+1105A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972626 | |||||||
chr3:124972690 | G | C | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3996+1041C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124972690 | |||||||
chr3:124973007 | T | G | 167 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(164): Show |
172 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.3996+724A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973007 | |||||||
chr3:124973008 | A | T | 167 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(164): Show |
172 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.3996+723T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973008 | |||||||
chr3:124973015 | C | CTAT | 91 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0002c0003t0002g0157 others(88): Show |
96 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.3996+713_3996+715d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973015 | |||||||
chr3:124973056 | C | T | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3996+675G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973056 | |||||||
chr3:124973155 | A | G | 256 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(253): Show |
266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.3996+576T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973155 | |||||||
chr3:124973173 | C | T | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3996+558G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973173 | |||||||
chr3:124973202 | G | T | 99 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0070g0195 others(96): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3996+529C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973202 | |||||||
chr3:124973315 | G | A | 6 | a0001c0001t0070g0195 a0002c0081t0116g0244 a0002c0082t0069g0193 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3996+416C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973315 | |||||||
chr3:124973350 | T | C | 97 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0070g0195 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3996+381A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973350 | |||||||
chr3:124973570 | T | C | 1 | a0010c0008t0027g0235 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3996+161A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 16/16 | chr3 | 124973570 | |||||||
chr3:124973941 | C | T | 255 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(252): Show |
265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.3822-36G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124973941 | |||||||
chr3:124974210 | C | T | 1 | a0002c0005t0011g0198 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3822-305G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974210 | |||||||
chr3:124974455 | G | T | 256 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(253): Show |
266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.3822-550C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974455 | |||||||
chr3:124974494 | C | T | 1 | a0001c0001t0098g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3822-589G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974494 | |||||||
chr3:124974674 | C | T | 102 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(99): Show |
103 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.3822-769G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974674 | |||||||
chr3:124974690 | A | T | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-785T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974690 | |||||||
chr3:124974754 | G | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-849C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974754 | |||||||
chr3:124974833 | G | A | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-928C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974833 | |||||||
chr3:124974960 | C | T | 3 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0026c0058t0057g0219 |
4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3822-1055G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974960 | |||||||
chr3:124974982 | C | T | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1077G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974982 | |||||||
chr3:124974999 | G | A | 1 | a0006c0015t0005g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3822-1094C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124974999 | |||||||
chr3:124975038 | T | A | 1 | a0001c0020t0029g0015 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3822-1133A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975038 | |||||||
chr3:124975079 | G | A | 1 | a0001c0001t0095g0102 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3822-1174C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975079 | |||||||
chr3:124975159 | G | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1254C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975159 | |||||||
chr3:124975221 | A | G | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1316T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975221 | |||||||
chr3:124975247 | C | T | 1 | a0001c0002t0072g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3822-1342G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975247 | |||||||
chr3:124975364 | C | G | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1459G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975364 | |||||||
chr3:124975459 | C | T | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1554G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975459 | |||||||
chr3:124975524 | A | G | 1 | a0001c0001t0061g0288 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3822-1619T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975524 | |||||||
chr3:124975558 | G | A | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1653C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975558 | |||||||
chr3:124975634 | C | G | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1729G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975634 | |||||||
chr3:124975695 | T | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1790A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975695 | |||||||
chr3:124975842 | T | C | 1 | a0001c0010t0107g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3822-1937A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975842 | |||||||
chr3:124975875 | G | A | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3822-1970C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975875 | |||||||
chr3:124975902 | T | A | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1957A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975902 | |||||||
chr3:124975975 | G | A | 1 | a0004c0007t0129g0345 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3821+1884C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975975 | |||||||
chr3:124975985 | G | A | 1 | a0001c0001t0099g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3821+1874C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124975985 | |||||||
chr3:124976034 | G | A | 23 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(20): Show |
26 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.3821+1825C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976034 | |||||||
chr3:124976093 | G | A | 1 | a0010c0008t0036g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3821+1766C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976093 | |||||||
chr3:124976187 | G | A | 92 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0002c0003t0002g0157 others(89): Show |
97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3821+1672C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976187 | |||||||
chr3:124976250 | T | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1609A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976250 | |||||||
chr3:124976259 | G | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1600C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976259 | |||||||
chr3:124976268 | C | A | 1 | a0028c0090t0119g0348 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3821+1591G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976268 | |||||||
chr3:124976270 | T | G | 2 | a0001c0002t0016g0047 a0001c0002t0033g0046 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3821+1589A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976270 | |||||||
chr3:124976497 | AT | A | 163 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(160): Show |
168 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.3821+1361delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976497 | |||||||
chr3:124976610 | C | T | 1 | a0005c0086t0090g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3821+1249G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976610 | |||||||
chr3:124976733 | G | T | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1126C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976733 | |||||||
chr3:124976840 | T | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+1019A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976840 | |||||||
chr3:124976882 | C | T | 3 | a0002c0003t0007g0149 a0006c0011t0011g0061 a0006c0011t0011g0125 |
3 | HG00642.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3821+977G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976882 | |||||||
chr3:124976964 | G | A | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+895C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976964 | |||||||
chr3:124976977 | T | C | 1 | a0024c0032t0065g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3821+882A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124976977 | |||||||
chr3:124977068 | C | CATGATAG others(3): Show |
159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+781_3821+790d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977068 | |||||||
chr3:124977212 | C | T | 54 | a0001c0001t0070g0195 a0001c0001t0077g0044 a0001c0001t0126g0272 others(51): Show |
57 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3821+647G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977212 | |||||||
chr3:124977335 | T | C | 159 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(156): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3821+524A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977335 | |||||||
chr3:124977667 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3821+192A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977667 | |||||||
chr3:124977714 | C | T | 1 | a0005c0006t0088g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3821+145G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 15/16 | chr3 | 124977714 | |||||||
chr3:124977953 | G | A | 1 | a0009c0022t0062g0229 | 1 | NA19054.hp2 | splice_region_variant&intron_variant | LOW | c.3734-7C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124977953 | |||||||
chr3:124977963 | CA | C | 102 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(99): Show |
103 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.3734-18delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124977963 | |||||||
chr3:124978100 | A | G | 1 | a0001c0002t0049g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3734-154T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978100 | |||||||
chr3:124978141 | G | T | 4 | a0001c0001t0070g0195 a0019c0026t0053g0302 a0019c0026t0053g0303 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734-195C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978141 | |||||||
chr3:124978383 | T | G | 164 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(161): Show |
169 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.3734-437A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978383 | |||||||
chr3:124978639 | T | C | 1 | a0001c0001t0127g0299 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3734-693A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978639 | |||||||
chr3:124978763 | T | G | 1 | a0007c0013t0124g0232 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3734-817A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978763 | |||||||
chr3:124978802 | A | AAAAT | 143 | a0001c0001t0007g0114 a0001c0001t0008g0245 a0001c0001t0008g0248 others(140): Show |
145 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.3734-860_3734-857d others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | |||||||
chr3:124978802 | A | AAAATAAA others(1): Show |
109 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(106): Show |
114 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.3734-864_3734-857d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | |||||||
chr3:124978802 | A | AAAATAAA others(5): Show |
27 | a0001c0001t0097g0145 a0002c0003t0006g0265 a0002c0028t0080g0029 others(24): Show |
29 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.3734-868_3734-857d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | |||||||
chr3:124978802 | AAAATAAA others(1): Show |
A | 7 | a0003c0004t0040g0175 a0003c0004t0040g0176 a0026c0059t0058g0220 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3734-864_3734-857d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | |||||||
chr3:124978802 | AAAATAAA others(5): Show |
A | 2 | a0002c0005t0028g0257 a0043c0092t0133g0314 |
2 | HG03139.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3734-868_3734-857d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978802 | |||||||
chr3:124978956 | C | CT | 12 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3734-1011dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978956 | |||||||
chr3:124978987 | G | A | 2 | a0003c0068t0084g0197 a0005c0006t0009g0043 |
2 | HG00738.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3734-1041C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124978987 | |||||||
chr3:124979019 | C | T | 1 | a0008c0027t0140g0329 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3734-1073G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979019 | |||||||
chr3:124979140 | C | T | 2 | a0005c0086t0090g0085 a0006c0076t0091g0162 |
2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3734-1194G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979140 | |||||||
chr3:124979148 | C | T | 92 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0002c0003t0002g0157 others(89): Show |
97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3734-1202G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979148 | |||||||
chr3:124979613 | T | C | 2 | a0005c0086t0090g0085 a0006c0076t0091g0162 |
2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3734-1667A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979613 | |||||||
chr3:124979760 | C | T | 28 | a0001c0001t0126g0272 a0001c0001t0127g0299 a0002c0003t0002g0157 others(25): Show |
31 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.3734-1814G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124979760 | |||||||
chr3:124980299 | T | A | 1 | a0002c0082t0069g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3734-2353A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980299 | |||||||
chr3:124980358 | A | T | 13 | a0001c0001t0044g0104 a0001c0001t0044g0161 a0001c0001t0045g0129 others(10): Show |
13 | HG01071.hp2 HG01106.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.3734-2412T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980358 | |||||||
chr3:124980402 | T | G | 256 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(253): Show |
266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.3734-2456A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980402 | |||||||
chr3:124980497 | C | T | 5 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0015c0057t0128g0210 others(2): Show |
6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3734-2551G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980497 | |||||||
chr3:124980549 | C | T | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-2603G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980549 | |||||||
chr3:124980665 | C | T | 5 | a0002c0003t0003g0005 a0002c0003t0003g0006 a0002c0003t0003g0106 others(2): Show |
7 | HG00544.hp2 NA18944.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.3734-2719G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980665 | |||||||
chr3:124980871 | T | G | 1 | a0020c0043t0063g0340 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3734-2925A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124980871 | |||||||
chr3:124981004 | C | T | 1 | a0003c0004t0014g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3734-3058G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981004 | |||||||
chr3:124981014 | G | T | 1 | a0001c0002t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3734-3068C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981014 | |||||||
chr3:124981064 | C | G | 50 | a0001c0001t0070g0195 a0001c0001t0077g0044 a0002c0003t0007g0070 others(47): Show |
53 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.3734-3118G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981064 | |||||||
chr3:124981071 | C | T | 255 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(252): Show |
265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.3734-3125G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981071 | |||||||
chr3:124981233 | C | CT | 179 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0126g0272 others(176): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.3734-3288dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981233 | |||||||
chr3:124981233 | C | CTTT | 51 | a0001c0001t0070g0195 a0001c0001t0077g0044 a0002c0003t0007g0070 others(48): Show |
55 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.3734-3290_3734-328 others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981233 | |||||||
chr3:124981248 | A | T | 99 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(96): Show |
100 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3734-3302T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981248 | |||||||
chr3:124981251 | G | A | 99 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(96): Show |
100 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3734-3305C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981251 | |||||||
chr3:124981251 | GT | G | 59 | a0001c0001t0004g0293 a0001c0001t0008g0246 a0001c0001t0008g0292 others(56): Show |
63 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.3734-3306delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981251 | |||||||
chr3:124981252 | T | G | 99 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(96): Show |
100 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.3734-3306A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981252 | |||||||
chr3:124981350 | G | C | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-3404C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981350 | |||||||
chr3:124981492 | C | T | 1 | a0001c0002t0103g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3734-3546G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981492 | |||||||
chr3:124981549 | A | G | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-3603T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981549 | |||||||
chr3:124981566 | C | T | 1 | a0006c0011t0011g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3734-3620G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981566 | |||||||
chr3:124981570 | G | A | 6 | a0001c0001t0126g0272 a0001c0001t0127g0299 a0003c0004t0040g0175 others(3): Show |
6 | HG01192.hp1 HG01891.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3734-3624C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981570 | |||||||
chr3:124981868 | A | C | 157 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(154): Show |
162 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.3734-3922T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981868 | |||||||
chr3:124981871 | C | T | 1 | a0002c0005t0010g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3734-3925G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981871 | |||||||
chr3:124981912 | ATT | A | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-3968_3734-396 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981912 | |||||||
chr3:124981945 | C | T | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3734-3999G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981945 | |||||||
chr3:124981946 | A | G | 105 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(102): Show |
106 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.3734-4000T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124981946 | |||||||
chr3:124982142 | C | T | 1 | a0014c0054t0110g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3734-4196G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982142 | |||||||
chr3:124982265 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3734-4319A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982265 | |||||||
chr3:124982274 | G | C | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-4328C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982274 | |||||||
chr3:124982333 | T | A | 1 | a0026c0058t0057g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3734-4387A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982333 | |||||||
chr3:124982344 | T | C | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-4398A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982344 | |||||||
chr3:124982390 | C | T | 4 | a0001c0001t0093g0163 a0002c0005t0010g0166 a0018c0088t0010g0178 others(1): Show |
4 | HG01109.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3734-4444G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982390 | |||||||
chr3:124982426 | G | A | 1 | a0027c0047t0108g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3734-4480C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982426 | |||||||
chr3:124982603 | A | G | 1 | a0003c0004t0002g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3734-4657T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982603 | |||||||
chr3:124982646 | G | C | 4 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0020c0043t0063g0340 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734-4700C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982646 | |||||||
chr3:124982762 | C | T | 1 | a0009c0056t0143g0209 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3734-4816G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982762 | |||||||
chr3:124982964 | TG | T | 4 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0015c0057t0128g0210 others(1): Show |
5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3734-5019delC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124982964 | |||||||
chr3:124983087 | C | A | 1 | a0001c0010t0001g0014 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3734-5141G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983087 | |||||||
chr3:124983160 | C | A | 1 | a0004c0007t0129g0345 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3734-5214G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983160 | |||||||
chr3:124983164 | C | A | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5218G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983164 | |||||||
chr3:124983203 | C | T | 1 | a0005c0006t0002g0099 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3734-5257G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983203 | |||||||
chr3:124983338 | T | C | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5392A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983338 | |||||||
chr3:124983346 | CT | C | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5401delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983346 | |||||||
chr3:124983407 | T | G | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5461A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983407 | |||||||
chr3:124983421 | C | CA | 157 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(154): Show |
162 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.3734-5476dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983421 | |||||||
chr3:124983423 | C | A | 1 | a0001c0001t0004g0293 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3734-5477G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983423 | |||||||
chr3:124983463 | C | T | 251 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(248): Show |
257 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.3734-5517G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983463 | |||||||
chr3:124983501 | A | AT | 160 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0277 others(157): Show |
165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3734-5556dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983501 | |||||||
chr3:124983580 | C | T | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3734-5634G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983580 | |||||||
chr3:124983605 | G | C | 1 | a0001c0001t0011g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3734-5659C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983605 | |||||||
chr3:124983700 | C | T | 1 | a0003c0004t0002g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3734-5754G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983700 | |||||||
chr3:124983754 | C | T | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3734-5808G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983754 | |||||||
chr3:124983791 | T | C | 1 | a0001c0001t0099g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3734-5845A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983791 | |||||||
chr3:124983794 | T | C | 1 | a0002c0035t0001g0103 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3734-5848A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983794 | |||||||
chr3:124983808 | T | C | 4 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0020c0043t0063g0340 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734-5862A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124983808 | |||||||
chr3:124984173 | G | A | 2 | a0001c0001t0126g0272 a0001c0001t0127g0299 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3734-6227C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984173 | |||||||
chr3:124984177 | G | T | 2 | a0005c0006t0009g0142 a0017c0029t0020g0035 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3734-6231C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984177 | |||||||
chr3:124984215 | G | T | 6 | a0001c0001t0126g0272 a0001c0001t0127g0299 a0003c0004t0040g0175 others(3): Show |
6 | HG01192.hp1 HG01891.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3734-6269C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984215 | |||||||
chr3:124984263 | C | G | 160 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(157): Show |
165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3734-6317G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984263 | |||||||
chr3:124984270 | C | T | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3734-6324G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984270 | |||||||
chr3:124984359 | C | CAT | 160 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(157): Show |
165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3734-6414_3734-641 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984359 | |||||||
chr3:124984381 | T | C | 5 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0015c0057t0128g0210 others(2): Show |
6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+6406A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984381 | |||||||
chr3:124984450 | G | A | 6 | a0001c0001t0070g0195 a0002c0081t0116g0244 a0002c0082t0069g0193 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3733+6337C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984450 | |||||||
chr3:124984512 | G | A | 2 | a0001c0001t0006g0280 a0001c0001t0006g0281 |
2 | HG00609.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3733+6275C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984512 | |||||||
chr3:124984575 | A | T | 2 | a0003c0004t0039g0054 a0003c0045t0039g0028 |
2 | HG02735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3733+6212T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984575 | |||||||
chr3:124984604 | C | T | 1 | a0005c0006t0118g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3733+6183G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984604 | |||||||
chr3:124984684 | G | A | 1 | a0001c0001t0018g0251 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3733+6103C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984684 | |||||||
chr3:124984753 | C | G | 49 | a0001c0001t0070g0195 a0001c0001t0077g0044 a0002c0003t0007g0070 others(46): Show |
52 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.3733+6034G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984753 | |||||||
chr3:124984849 | A | C | 93 | a0001c0002t0001g0075 a0001c0002t0001g0080 a0001c0002t0001g0092 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.3733+5938T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124984849 | |||||||
chr3:124985033 | G | A | 2 | a0004c0007t0060g0332 a0004c0007t0137g0335 |
2 | HG02155.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3733+5754C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985033 | |||||||
chr3:124985062 | G | A | 1 | a0047c0078t0015g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3733+5725C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985062 | |||||||
chr3:124985211 | A | G | 2 | a0001c0001t0126g0272 a0001c0001t0127g0299 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3733+5576T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985211 | |||||||
chr3:124985216 | G | A | 1 | a0018c0037t0063g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3733+5571C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985216 | |||||||
chr3:124985380 | A | C | 1 | a0003c0004t0002g0170 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3733+5407T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985380 | |||||||
chr3:124985402 | AT | A | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+5384delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985402 | |||||||
chr3:124985405 | T | G | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+5382A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985405 | |||||||
chr3:124985589 | G | A | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.3733+5198C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985589 | |||||||
chr3:124985797 | T | G | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+4990A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124985797 | |||||||
chr3:124986131 | G | A | 2 | a0001c0001t0006g0280 a0001c0001t0006g0281 |
2 | HG00609.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3733+4656C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986131 | |||||||
chr3:124986267 | A | G | 259 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3733+4520T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986267 | |||||||
chr3:124986368 | A | G | 160 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(157): Show |
165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3733+4419T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986368 | |||||||
chr3:124986411 | T | G | 160 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(157): Show |
165 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.3733+4376A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986411 | |||||||
chr3:124986497 | C | T | 1 | a0001c0001t0008g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3733+4290G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986497 | |||||||
chr3:124986583 | T | C | 2 | a0002c0081t0116g0244 a0002c0082t0069g0193 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3733+4204A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986583 | |||||||
chr3:124986658 | G | A | 2 | a0005c0006t0002g0179 a0013c0087t0021g0091 |
2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.3733+4129C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986658 | |||||||
chr3:124986819 | G | T | 1 | a0019c0026t0117g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3733+3968C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124986819 | |||||||
chr3:124987108 | C | T | 1 | a0001c0001t0099g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3733+3679G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987108 | |||||||
chr3:124987290 | T | C | 1 | a0037c0050t0022g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3733+3497A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987290 | |||||||
chr3:124987374 | G | GCCACACC others(1): Show |
9 | a0006c0011t0011g0061 a0006c0011t0011g0125 a0008c0009t0004g0328 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3733+3405_3733+341 others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987374 | |||||||
chr3:124987474 | C | G | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3733+3313G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987474 | |||||||
chr3:124987570 | C | T | 108 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(105): Show |
109 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.3733+3217G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987570 | |||||||
chr3:124987577 | C | CA | 5 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0015c0057t0128g0210 others(2): Show |
6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+3209dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987577 | |||||||
chr3:124987579 | A | G | 1 | a0008c0009t0061g0319 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3733+3208T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987579 | |||||||
chr3:124987630 | T | TCTC | 161 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(158): Show |
166 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.3733+3156_3733+315 others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987630 | |||||||
chr3:124987789 | A | G | 258 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(255): Show |
264 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.3733+2998T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987789 | |||||||
chr3:124987847 | A | G | 3 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0026c0058t0057g0219 |
4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2940T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987847 | |||||||
chr3:124987924 | T | TAC | 5 | a0005c0006t0009g0142 a0005c0006t0054g0247 a0016c0025t0130g0316 others(2): Show |
5 | HG00323.hp1 HG01106.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2861_3733+286 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACAC | 3 | a0003c0004t0040g0176 a0005c0006t0022g0089 a0030c0080t0085g0087 |
3 | HG01891.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3733+2857_3733+286 others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(3): Show |
1 | a0005c0086t0090g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3733+2853_3733+286 others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(7): Show |
10 | a0001c0001t0007g0114 a0001c0001t0018g0251 a0001c0001t0029g0154 others(7): Show |
10 | HG00639.hp2 HG01081.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.3733+2849_3733+286 others(18): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(9): Show |
13 | a0001c0001t0044g0104 a0001c0001t0097g0145 a0001c0001t0100g0096 others(10): Show |
13 | HG01243.hp2 HG01256.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.3733+2847_3733+286 others(20): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(11): Show |
6 | a0001c0001t0059g0260 a0001c0001t0070g0195 a0001c0001t0127g0299 others(3): Show |
6 | HG01109.hp2 HG01192.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.3733+2845_3733+286 others(22): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(13): Show |
5 | a0002c0081t0116g0244 a0010c0008t0004g0236 a0021c0023t0031g0191 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2843_3733+286 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(15): Show |
3 | a0021c0023t0031g0190 a0027c0047t0108g0017 a0035c0066t0068g0011 |
3 | HG02615.hp1 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3733+2841_3733+286 others(26): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | T | TACACACA others(17): Show |
3 | a0002c0082t0069g0193 a0021c0023t0031g0183 a0036c0069t0111g0202 |
3 | HG02630.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3733+2839_3733+286 others(28): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987924 | TAC | T | 57 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(54): Show |
60 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.3733+2861_3733+286 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987924 | |||||||
chr3:124987944 | C | T | 2 | a0001c0002t0024g0093 a0001c0002t0024g0094 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3733+2843G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987944 | |||||||
chr3:124987952 | C | CACACACA others(39): Show |
1 | a0004c0007t0013g0336 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(45): Show |
1 | a0008c0027t0144g0326 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(56): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(47): Show |
1 | a0002c0014t0121g0255 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(33): Show |
1 | a0001c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
1 | a0002c0003t0015g0084 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(37): Show |
1 | a0001c0002t0038g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(41): Show |
3 | a0001c0001t0077g0044 a0001c0002t0001g0144 a0009c0016t0005g0221 |
3 | HG02083.hp2 HG02523.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
1 | a0004c0007t0060g0333 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(31): Show |
2 | a0002c0003t0007g0070 a0002c0003t0074g0076 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
1 | a0005c0006t0118g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(39): Show |
2 | a0025c0036t0030g0068 a0025c0036t0030g0120 |
2 | HG02132.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(47): Show |
1 | a0001c0002t0038g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(21): Show |
1 | a0017c0029t0007g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(32): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
3 | a0002c0003t0007g0077 a0004c0007t0060g0332 a0029c0075t0076g0182 |
3 | HG01255.hp1 HG02155.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(31): Show |
3 | a0004c0007t0137g0335 a0012c0030t0048g0037 a0028c0090t0119g0348 |
3 | HG00639.hp1 HG01517.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(33): Show |
8 | a0002c0003t0007g0071 a0002c0014t0120g0261 a0004c0007t0013g0305 others(5): Show |
9 | HG01243.hp1 HG02135.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
2 | a0001c0002t0005g0296 a0007c0012t0013g0226 |
2 | HG02559.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(37): Show |
3 | a0007c0012t0017g0002 a0012c0019t0102g0205 a0046c0063t0005g0237 |
3 | HG03710.hp2 NA19055.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(39): Show |
2 | a0001c0002t0005g0290 a0001c0002t0024g0116 |
2 | HG00642.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(41): Show |
2 | a0001c0010t0001g0023 a0001c0010t0033g0020 |
2 | HG02293.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(43): Show |
1 | a0001c0002t0104g0180 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(54): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(45): Show |
3 | a0001c0002t0005g0291 a0001c0002t0024g0139 a0012c0030t0048g0038 |
3 | HG01168.hp2 HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(56): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(27): Show |
1 | a0004c0007t0136g0317 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
7 | a0001c0010t0107g0021 a0002c0003t0007g0083 a0002c0003t0007g0101 others(4): Show |
7 | HG01884.hp1 HG02074.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(31): Show |
1 | a0004c0039t0017g0338 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(33): Show |
4 | a0001c0002t0005g0253 a0002c0003t0046g0118 a0002c0014t0075g0079 others(1): Show |
4 | HG02148.hp2 NA18988.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
4 | a0001c0002t0051g0138 a0001c0002t0112g0150 a0002c0014t0015g0117 others(1): Show |
4 | HG01256.hp1 NA18968.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(37): Show |
6 | a0001c0002t0001g0131 a0001c0002t0145g0351 a0004c0039t0017g0323 others(3): Show |
6 | HG01071.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(39): Show |
1 | a0001c0010t0001g0014 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(41): Show |
1 | a0012c0019t0001g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(45): Show |
2 | a0001c0002t0001g0130 a0001c0002t0001g0143 |
2 | HG01928.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(56): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(47): Show |
1 | a0006c0015t0115g0056 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(13): Show |
14 | a0001c0001t0008g0292 a0001c0001t0047g0123 a0001c0001t0047g0124 others(11): Show |
14 | HG00621.hp1 HG00642.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(27): Show |
1 | a0001c0002t0001g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
2 | a0001c0002t0001g0092 a0001c0002t0072g0134 |
2 | HG03669.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(31): Show |
3 | a0001c0002t0001g0121 a0001c0002t0052g0136 a0008c0027t0005g0331 |
3 | HG03239.hp1 NA18950.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(33): Show |
2 | a0001c0002t0024g0094 a0003c0034t0030g0115 |
2 | HG03239.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
2 | a0001c0002t0024g0093 a0012c0019t0114g0204 |
2 | HG03491.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(37): Show |
6 | a0001c0002t0001g0097 a0001c0002t0016g0052 a0001c0002t0033g0051 others(3): Show |
6 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(39): Show |
2 | a0001c0002t0105g0140 a0001c0010t0001g0026 |
2 | HG04115.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(50): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(41): Show |
1 | a0001c0002t0051g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(43): Show |
1 | a0002c0035t0001g0103 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(54): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(47): Show |
1 | a0001c0002t0049g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(58): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(22): Show |
1 | a0006c0015t0050g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(33): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(11): Show |
29 | a0001c0001t0004g0293 a0001c0001t0011g0184 a0001c0001t0012g0173 others(26): Show |
29 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(22): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(13): Show |
3 | a0002c0005t0028g0257 a0004c0040t0059g0313 a0013c0017t0045g0132 |
3 | HG02486.hp1 NA18939.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(15): Show |
1 | a0001c0001t0044g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(26): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(25): Show |
1 | a0001c0002t0106g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(36): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(27): Show |
1 | a0001c0002t0050g0199 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
1 | a0047c0078t0015g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(33): Show |
5 | a0001c0002t0001g0108 a0001c0002t0005g0300 a0001c0002t0016g0146 others(2): Show |
5 | HG01074.hp1 HG01099.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(44): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
1 | a0001c0002t0103g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(37): Show |
1 | a0001c0002t0016g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(48): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(9): Show |
20 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(17): Show |
20 | HG01106.hp1 HG01884.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(20): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(13): Show |
1 | a0001c0001t0010g0069 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(23): Show |
2 | a0005c0006t0088g0066 a0015c0057t0128g0210 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(34): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
1 | a0014c0054t0110g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(31): Show |
3 | a0001c0010t0001g0031 a0006c0011t0086g0081 a0009c0016t0141g0223 |
3 | HG02698.hp1 HG03486.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(42): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
1 | a0032c0064t0067g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(7): Show |
16 | a0001c0001t0008g0246 a0001c0001t0008g0248 a0001c0001t0008g0264 others(13): Show |
17 | HG00438.hp2 HG01346.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(18): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(9): Show |
1 | a0006c0011t0011g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(20): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(11): Show |
3 | a0001c0001t0008g0242 a0001c0001t0008g0245 a0006c0011t0010g0194 |
3 | HG01109.hp1 HG02293.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(22): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(17): Show |
1 | a0001c0002t0032g0007 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(28): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(19): Show |
2 | a0001c0002t0005g0298 a0001c0002t0032g0007 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(30): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(23): Show |
1 | a0009c0016t0038g0218 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(34): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(25): Show |
2 | a0001c0002t0001g0075 a0001c0002t0001g0080 |
2 | NA18942.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(36): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(27): Show |
1 | a0006c0011t0022g0003 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3733+2834_3733+283 others(38): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(29): Show |
1 | a0014c0053t0001g0034 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(40): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(13): Show |
1 | a0001c0002t0032g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(24): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(3): Show |
1 | a0001c0001t0095g0102 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(25): Show |
1 | a0002c0035t0001g0155 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(36): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CACACACA others(35): Show |
1 | a0039c0095t0057g0315 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3733+2834_3733+283 others(46): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | CAT | 5 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0005c0006t0014g0268 others(2): Show |
5 | HG00609.hp1 HG02132.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.3733+2833_3733+283 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987952 | C | T | 3 | a0002c0003t0082g0185 a0003c0045t0039g0028 a0003c0068t0084g0197 |
3 | HG00738.hp1 HG02735.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3733+2835G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987952 | |||||||
chr3:124987954 | T | C | 25 | a0001c0001t0070g0195 a0001c0001t0126g0272 a0001c0001t0127g0299 others(22): Show |
26 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.3733+2833A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987954 | |||||||
chr3:124987956 | T | C | 14 | a0001c0001t0126g0272 a0001c0001t0127g0299 a0007c0060t0139g0217 others(11): Show |
15 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3733+2831A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987956 | |||||||
chr3:124987958 | T | C | 6 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0019c0026t0053g0302 others(3): Show |
7 | HG00735.hp2 HG01074.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3733+2829A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987958 | |||||||
chr3:124987960 | T | C | 3 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0026c0058t0057g0219 |
4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2827A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987960 | |||||||
chr3:124987962 | T | C | 3 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0026c0058t0057g0219 |
4 | HG00735.hp2 HG01074.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2825A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124987962 | |||||||
chr3:124988018 | A | C | 237 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(234): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3733+2769T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988018 | |||||||
chr3:124988211 | G | C | 5 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0015c0057t0128g0210 others(2): Show |
6 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+2576C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988211 | |||||||
chr3:124988306 | A | G | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3733+2481T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988306 | |||||||
chr3:124988431 | A | G | 237 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(234): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3733+2356T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988431 | |||||||
chr3:124988455 | T | C | 1 | a0001c0001t0061g0288 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3733+2332A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988455 | |||||||
chr3:124988601 | T | C | 2 | a0022c0024t0037g0008 a0022c0024t0037g0263 |
3 | NA18944.hp1 NA18973.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3733+2186A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988601 | |||||||
chr3:124988744 | C | T | 4 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0020c0043t0063g0340 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+2043G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988744 | |||||||
chr3:124988745 | C | A | 2 | a0003c0004t0081g0177 a0004c0007t0123g0349 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3733+2042G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988745 | |||||||
chr3:124988866 | G | A | 4 | a0010c0008t0004g0236 a0010c0008t0036g0238 a0010c0008t0036g0239 others(1): Show |
4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+1921C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988866 | |||||||
chr3:124988933 | A | G | 4 | a0026c0059t0058g0220 a0027c0047t0108g0017 a0035c0066t0068g0011 others(1): Show |
4 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3733+1854T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988933 | |||||||
chr3:124988951 | C | T | 204 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(201): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.3733+1836G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124988951 | |||||||
chr3:124989446 | T | C | 3 | a0011c0041t0035g0309 a0011c0041t0035g0311 a0042c0091t0122g0310 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3733+1341A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989446 | |||||||
chr3:124989506 | CA | C | 204 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(201): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.3733+1280delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989506 | |||||||
chr3:124989718 | C | G | 1 | a0026c0058t0057g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3733+1069G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989718 | |||||||
chr3:124989738 | A | G | 237 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(234): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3733+1049T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989738 | |||||||
chr3:124989815 | G | C | 1 | a0040c0065t0066g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3733+972C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989815 | |||||||
chr3:124989923 | T | C | 1 | a0001c0002t0038g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3733+864A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989923 | |||||||
chr3:124989985 | T | C | 204 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(201): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.3733+802A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124989985 | |||||||
chr3:124990082 | C | A | 10 | a0005c0086t0090g0085 a0006c0076t0091g0162 a0021c0023t0031g0183 others(7): Show |
10 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3733+705G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990082 | |||||||
chr3:124990084 | C | T | 1 | a0001c0001t0007g0114 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3733+703G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990084 | |||||||
chr3:124990141 | T | C | 3 | a0011c0041t0035g0309 a0011c0041t0035g0311 a0042c0091t0122g0310 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3733+646A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990141 | |||||||
chr3:124990341 | G | GT | 6 | a0001c0001t0004g0275 a0001c0001t0008g0292 a0002c0003t0007g0077 others(3): Show |
6 | NA18946.hp2 NA18966.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.3733+445dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990341 | |||||||
chr3:124990341 | GT | G | 90 | a0001c0002t0001g0075 a0001c0002t0001g0080 a0001c0002t0001g0092 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.3733+445delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990341 | |||||||
chr3:124990407 | T | C | 258 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(255): Show |
264 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.3733+380A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990407 | |||||||
chr3:124990528 | G | A | 1 | a0003c0004t0002g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3733+259C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990528 | |||||||
chr3:124990570 | C | A | 4 | a0010c0008t0004g0236 a0010c0008t0036g0238 a0010c0008t0036g0239 others(1): Show |
4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3733+217G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990570 | |||||||
chr3:124990592 | A | G | 1 | a0004c0007t0129g0345 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3733+195T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990592 | |||||||
chr3:124990652 | C | T | 1 | a0021c0023t0031g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3733+135G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990652 | |||||||
chr3:124990654 | C | A | 1 | a0001c0002t0001g0108 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3733+133G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 14/16 | chr3 | 124990654 | |||||||
chr3:124991054 | G | A | 37 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(34): Show |
38 | HG00438.hp2 HG00639.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.3653-68C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991054 | |||||||
chr3:124991150 | C | CT | 132 | a0001c0001t0070g0195 a0001c0001t0077g0044 a0001c0002t0001g0075 others(129): Show |
137 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.3653-165dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991150 | |||||||
chr3:124991163 | T | C | 1 | a0048c0094t0004g0330 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3653-177A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991163 | |||||||
chr3:124991163 | T | TC | 104 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(101): Show |
105 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3653-178_3653-177i others(3): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991163 | |||||||
chr3:124991180 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3653-194G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991180 | |||||||
chr3:124991228 | C | T | 1 | a0006c0076t0091g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3653-242G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991228 | |||||||
chr3:124991248 | C | T | 105 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(102): Show |
106 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.3653-262G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991248 | |||||||
chr3:124991337 | A | G | 1 | a0004c0007t0060g0333 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3653-351T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991337 | |||||||
chr3:124991397 | C | T | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3653-411G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991397 | |||||||
chr3:124991528 | T | C | 237 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(234): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3653-542A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991528 | |||||||
chr3:124991796 | G | A | 15 | a0005c0086t0090g0085 a0006c0076t0091g0162 a0007c0060t0139g0217 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3653-810C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991796 | |||||||
chr3:124991833 | C | T | 9 | a0006c0011t0011g0061 a0006c0011t0011g0125 a0008c0009t0004g0328 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3653-847G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991833 | |||||||
chr3:124991853 | G | A | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3653-867C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991853 | |||||||
chr3:124991991 | T | TC | 9 | a0002c0003t0003g0004 a0002c0003t0003g0005 a0002c0003t0003g0006 others(6): Show |
12 | HG00544.hp2 HG00673.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.3653-1006dupG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124991991 | |||||||
chr3:124992033 | A | C | 1 | a0007c0013t0004g0211 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3653-1047T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992033 | |||||||
chr3:124992124 | G | A | 1 | a0003c0004t0021g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3653-1138C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992124 | |||||||
chr3:124992163 | T | C | 1 | a0045c0073t0056g0297 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3653-1177A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992163 | |||||||
chr3:124992229 | G | T | 1 | a0027c0047t0108g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3653-1243C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992229 | |||||||
chr3:124992237 | G | A | 1 | a0002c0005t0042g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3653-1251C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992237 | |||||||
chr3:124992251 | A | G | 240 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(237): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.3653-1265T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992251 | |||||||
chr3:124992348 | A | G | 1 | a0028c0090t0119g0348 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3653-1362T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992348 | |||||||
chr3:124992491 | C | T | 19 | a0001c0001t0012g0173 a0001c0001t0042g0098 a0002c0005t0004g0276 others(16): Show |
19 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.3653-1505G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992491 | |||||||
chr3:124992527 | C | T | 107 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(104): Show |
108 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.3653-1541G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992527 | |||||||
chr3:124992542 | G | A | 107 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(104): Show |
108 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.3653-1556C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992542 | |||||||
chr3:124992991 | A | G | 2 | a0006c0015t0005g0267 a0006c0015t0049g0059 |
2 | HG00544.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3653-2005T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992991 | |||||||
chr3:124992992 | C | T | 10 | a0005c0086t0090g0085 a0006c0076t0091g0162 a0021c0023t0031g0183 others(7): Show |
10 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3653-2006G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124992992 | |||||||
chr3:124993024 | C | T | 1 | a0005c0006t0019g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3653-2038G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993024 | |||||||
chr3:124993122 | T | G | 32 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(29): Show |
34 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.3653-2136A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993122 | |||||||
chr3:124993188 | C | T | 1 | a0001c0001t0018g0251 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3653-2202G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993188 | |||||||
chr3:124993309 | T | C | 1 | a0002c0082t0069g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3653-2323A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993309 | |||||||
chr3:124993322 | C | T | 2 | a0003c0004t0002g0057 a0003c0004t0021g0058 |
2 | HG00438.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.3653-2336G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993322 | |||||||
chr3:124993324 | C | T | 1 | a0024c0032t0065g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3653-2338G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993324 | |||||||
chr3:124993352 | A | T | 51 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(48): Show |
52 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.3653-2366T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993352 | |||||||
chr3:124993412 | T | C | 1 | a0018c0037t0063g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3653-2426A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993412 | |||||||
chr3:124993466 | T | C | 256 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(253): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.3653-2480A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993466 | |||||||
chr3:124993485 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3653-2499G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993485 | |||||||
chr3:124993491 | T | C | 256 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(253): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.3653-2505A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993491 | |||||||
chr3:124993552 | A | G | 111 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(108): Show |
112 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.3653-2566T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993552 | |||||||
chr3:124993571 | A | G | 256 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(253): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.3653-2585T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993571 | |||||||
chr3:124993643 | G | A | 2 | a0001c0001t0126g0272 a0001c0001t0127g0299 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3653-2657C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993643 | |||||||
chr3:124993678 | C | G | 2 | a0011c0018t0034g0321 a0011c0018t0034g0327 |
2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.3653-2692G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993678 | |||||||
chr3:124993827 | G | C | 2 | a0007c0012t0013g0225 a0007c0012t0013g0226 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3653-2841C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993827 | |||||||
chr3:124993848 | T | C | 1 | a0010c0008t0034g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3653-2862A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124993848 | |||||||
chr3:124994074 | T | G | 1 | a0005c0006t0088g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3653-3088A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994074 | |||||||
chr3:124994179 | C | T | 1 | a0001c0001t0008g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3653-3193G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994179 | |||||||
chr3:124994496 | G | T | 110 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(107): Show |
111 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3652+3193C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994496 | |||||||
chr3:124994507 | C | CT | 10 | a0002c0033t0023g0164 a0002c0049t0087g0030 a0003c0004t0002g0090 others(7): Show |
11 | HG01346.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3652+3181dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994507 | |||||||
chr3:124994523 | G | T | 36 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(33): Show |
38 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.3652+3166C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994523 | |||||||
chr3:124994529 | G | A | 1 | a0001c0001t0047g0124 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3652+3160C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994529 | |||||||
chr3:124994566 | C | A | 112 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(109): Show |
113 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.3652+3123G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994566 | |||||||
chr3:124994784 | G | A | 1 | a0037c0050t0022g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3652+2905C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994784 | |||||||
chr3:124994839 | C | A | 83 | a0001c0001t0077g0044 a0001c0001t0113g0151 a0001c0002t0001g0075 others(80): Show |
85 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.3652+2850G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124994839 | |||||||
chr3:124995065 | G | A | 2 | a0017c0029t0007g0036 a0036c0069t0111g0202 |
2 | HG01433.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3652+2624C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995065 | |||||||
chr3:124995441 | G | A | 1 | a0002c0003t0003g0004 | 2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3652+2248C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995441 | |||||||
chr3:124995448 | G | T | 6 | a0001c0001t0070g0195 a0002c0081t0116g0244 a0002c0082t0069g0193 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3652+2241C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995448 | |||||||
chr3:124995522 | A | T | 1 | a0001c0001t0098g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3652+2167T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995522 | |||||||
chr3:124995552 | A | G | 1 | a0012c0019t0001g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3652+2137T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995552 | |||||||
chr3:124995636 | C | A | 1 | a0012c0019t0114g0204 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3652+2053G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995636 | |||||||
chr3:124995661 | C | G | 1 | a0041c0051t0023g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3652+2028G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995661 | |||||||
chr3:124995718 | G | A | 6 | a0001c0001t0070g0195 a0002c0081t0116g0244 a0002c0082t0069g0193 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3652+1971C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995718 | |||||||
chr3:124995931 | T | C | 4 | a0001c0002t0001g0092 a0001c0002t0024g0093 a0001c0002t0024g0094 others(1): Show |
4 | HG00140.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.3652+1758A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124995931 | |||||||
chr3:124996024 | C | A | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3652+1665G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996024 | |||||||
chr3:124996038 | T | C | 6 | a0001c0001t0070g0195 a0002c0081t0116g0244 a0002c0082t0069g0193 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3652+1651A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996038 | |||||||
chr3:124996079 | A | C | 1 | a0015c0057t0128g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3652+1610T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996079 | |||||||
chr3:124996124 | C | T | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3652+1565G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996124 | |||||||
chr3:124996145 | T | C | 250 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(247): Show |
256 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.3652+1544A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996145 | |||||||
chr3:124996146 | G | A | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3652+1543C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996146 | |||||||
chr3:124996153 | C | T | 1 | a0003c0067t0019g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3652+1536G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996153 | |||||||
chr3:124996155 | G | A | 1 | a0002c0005t0042g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3652+1534C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996155 | |||||||
chr3:124996156 | C | A | 1 | a0002c0005t0042g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3652+1533G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996156 | |||||||
chr3:124996178 | G | A | 1 | a0001c0002t0016g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3652+1511C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996178 | |||||||
chr3:124996180 | G | A | 2 | a0005c0086t0090g0085 a0037c0050t0022g0032 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3652+1509C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996180 | |||||||
chr3:124996188 | G | A | 40 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(37): Show |
42 | HG00733.hp1 HG01433.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.3652+1501C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996188 | |||||||
chr3:124996276 | G | A | 1 | a0010c0008t0034g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3652+1413C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996276 | |||||||
chr3:124996326 | T | C | 130 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(127): Show |
133 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3652+1363A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996326 | |||||||
chr3:124996330 | C | T | 40 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(37): Show |
42 | HG00733.hp1 HG01433.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.3652+1359G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996330 | |||||||
chr3:124996364 | G | T | 121 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(118): Show |
122 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.3652+1325C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996364 | |||||||
chr3:124996470 | T | A | 8 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0006c0077t0073g0088 others(5): Show |
10 | HG00735.hp2 HG01074.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3652+1219A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996470 | |||||||
chr3:124996485 | C | T | 2 | a0001c0001t0126g0272 a0001c0001t0127g0299 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3652+1204G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996485 | |||||||
chr3:124996648 | A | G | 8 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 others(5): Show |
8 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3652+1041T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996648 | |||||||
chr3:124996682 | T | C | 124 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(121): Show |
126 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.3652+1007A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996682 | |||||||
chr3:124996852 | A | G | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3652+837T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124996852 | |||||||
chr3:124997020 | G | C | 1 | a0001c0001t0012g0173 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3652+669C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997020 | |||||||
chr3:124997197 | A | G | 2 | a0011c0018t0056g0350 a0034c0061t0035g0222 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3652+492T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997197 | |||||||
chr3:124997200 | T | C | 122 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(119): Show |
124 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.3652+489A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997200 | |||||||
chr3:124997341 | C | A | 1 | a0001c0085t0132g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3652+348G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 12/16 | chr3 | 124997341 | |||||||
chr3:124997862 | C | T | 4 | a0004c0007t0013g0305 a0004c0007t0013g0312 a0004c0007t0025g0307 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3518-39G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124997862 | |||||||
chr3:124997916 | T | A | 4 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0020c0043t0063g0340 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3518-93A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124997916 | |||||||
chr3:124998045 | T | C | 128 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(125): Show |
131 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.3518-222A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998045 | |||||||
chr3:124998127 | T | G | 1 | a0005c0006t0004g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3518-304A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998127 | |||||||
chr3:124998213 | G | A | 49 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(46): Show |
51 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.3518-390C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998213 | |||||||
chr3:124998226 | G | A | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3518-403C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998226 | |||||||
chr3:124998250 | C | T | 1 | a0003c0004t0021g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3518-427G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998250 | |||||||
chr3:124998815 | C | T | 49 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(46): Show |
51 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.3518-992G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998815 | |||||||
chr3:124998921 | A | G | 1 | a0003c0004t0021g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3518-1098T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998921 | |||||||
chr3:124998951 | C | T | 3 | a0019c0026t0053g0302 a0019c0026t0053g0303 a0019c0026t0117g0304 |
3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3518-1128G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124998951 | |||||||
chr3:124999021 | C | T | 1 | a0040c0065t0066g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3518-1198G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999021 | |||||||
chr3:124999039 | A | C | 39 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(36): Show |
41 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.3518-1216T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999039 | |||||||
chr3:124999108 | C | T | 1 | a0006c0011t0011g0125 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3518-1285G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999108 | |||||||
chr3:124999224 | C | T | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3518-1401G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999224 | |||||||
chr3:124999234 | C | G | 2 | a0005c0086t0090g0085 a0037c0050t0022g0032 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3518-1411G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999234 | |||||||
chr3:124999525 | A | G | 130 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(127): Show |
133 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3518-1702T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999525 | |||||||
chr3:124999718 | C | T | 5 | a0001c0001t0070g0195 a0002c0082t0069g0193 a0019c0026t0053g0302 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3518-1895G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999718 | |||||||
chr3:124999925 | A | G | 179 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(176): Show |
184 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.3517+1927T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999925 | |||||||
chr3:124999932 | G | C | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3517+1920C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 124999932 | |||||||
chr3:125000132 | T | A | 1 | a0001c0002t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3517+1720A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000132 | |||||||
chr3:125000312 | G | A | 6 | a0001c0001t0044g0104 a0001c0001t0061g0288 a0001c0001t0100g0096 others(3): Show |
6 | HG01071.hp2 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3517+1540C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000312 | |||||||
chr3:125000598 | CT | C | 13 | a0002c0035t0001g0155 a0005c0086t0090g0085 a0007c0060t0139g0217 others(10): Show |
13 | HG01346.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3517+1253delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000598 | |||||||
chr3:125000609 | T | C | 1 | a0002c0003t0074g0076 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3517+1243A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000609 | |||||||
chr3:125000753 | C | T | 5 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0047t0108g0017 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3517+1099G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000753 | |||||||
chr3:125000843 | T | C | 179 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(176): Show |
184 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.3517+1009A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000843 | |||||||
chr3:125000893 | A | G | 3 | a0005c0006t0009g0142 a0005c0006t0054g0247 a0017c0029t0020g0035 |
3 | HG00323.hp1 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3517+959T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000893 | |||||||
chr3:125000923 | C | G | 1 | a0005c0006t0019g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3517+929G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125000923 | |||||||
chr3:125001071 | C | T | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3517+781G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001071 | |||||||
chr3:125001234 | CT | C | 53 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(50): Show |
55 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.3517+617delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001234 | |||||||
chr3:125001249 | A | G | 1 | a0002c0003t0003g0100 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3517+603T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001249 | |||||||
chr3:125001714 | T | A | 4 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0020c0043t0063g0340 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3517+138A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001714 | |||||||
chr3:125001818 | T | A | 1 | a0002c0003t0015g0084 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3517+34A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 11/16 | chr3 | 125001818 | |||||||
chr3:125002039 | A | G | 3 | a0006c0077t0073g0088 a0016c0025t0025g0009 a0016c0025t0130g0316 |
4 | HG00735.hp2 HG01074.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.3357-27T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 10/16 | chr3 | 125002039 | |||||||
chr3:125002057 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3357-45C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 10/16 | chr3 | 125002057 | |||||||
chr3:125002084 | T | C | 1 | a0002c0005t0135g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3357-72A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 10/16 | chr3 | 125002084 | |||||||
chr3:125002659 | C | T | 175 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(172): Show |
180 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(177): Show |
intron_variant | MODIFIER | c.3298-344G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002659 | |||||||
chr3:125002729 | C | T | 1 | a0003c0004t0009g0196 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3298-414G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002729 | |||||||
chr3:125002829 | T | C | 1 | a0002c0033t0094g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3298-514A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002829 | |||||||
chr3:125002947 | G | A | 126 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(123): Show |
129 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.3298-632C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125002947 | |||||||
chr3:125003123 | T | C | 8 | a0002c0003t0046g0118 a0002c0074t0071g0192 a0004c0007t0013g0336 others(5): Show |
8 | HG00597.hp2 HG02083.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.3298-808A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003123 | |||||||
chr3:125003177 | C | T | 79 | a0001c0001t0077g0044 a0001c0001t0113g0151 a0001c0002t0001g0075 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.3298-862G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003177 | |||||||
chr3:125003266 | T | C | 2 | a0002c0003t0046g0118 a0049c0083t0046g0119 |
2 | NA18991.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3298-951A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003266 | |||||||
chr3:125003385 | T | A | 1 | a0002c0003t0002g0157 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3298-1070A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003385 | |||||||
chr3:125003775 | T | G | 10 | a0001c0001t0126g0272 a0001c0001t0127g0299 a0006c0011t0022g0003 others(7): Show |
12 | HG00735.hp2 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.3298-1460A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003775 | |||||||
chr3:125003816 | C | A | 176 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(173): Show |
181 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.3297+1449G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003816 | |||||||
chr3:125003843 | C | T | 6 | a0001c0001t0070g0195 a0002c0081t0116g0244 a0002c0082t0069g0193 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3297+1422G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003843 | |||||||
chr3:125003917 | G | A | 1 | a0046c0063t0005g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3297+1348C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125003917 | |||||||
chr3:125004052 | G | A | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3297+1213C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004052 | |||||||
chr3:125004178 | T | C | 1 | a0037c0050t0022g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3297+1087A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004178 | |||||||
chr3:125004198 | C | T | 2 | a0003c0004t0014g0283 a0040c0065t0066g0013 |
2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3297+1067G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004198 | |||||||
chr3:125004294 | T | C | 39 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(36): Show |
41 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.3297+971A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004294 | |||||||
chr3:125004351 | A | G | 12 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3297+914T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004351 | |||||||
chr3:125004558 | C | A | 1 | a0024c0032t0065g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3297+707G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004558 | |||||||
chr3:125004716 | TA | T | 19 | a0001c0001t0008g0292 a0001c0001t0070g0195 a0001c0002t0024g0139 others(16): Show |
20 | HG01168.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3297+548delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004716 | |||||||
chr3:125004716 | TAA | T | 49 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(46): Show |
51 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.3297+547_3297+548d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004716 | |||||||
chr3:125004746 | G | A | 4 | a0002c0005t0011g0198 a0002c0005t0012g0113 a0002c0005t0012g0158 others(1): Show |
4 | HG00621.hp1 NA18747.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.3297+519C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004746 | |||||||
chr3:125004751 | G | C | 1 | a0004c0040t0028g0334 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3297+514C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004751 | |||||||
chr3:125004916 | A | G | 90 | a0001c0001t0077g0044 a0001c0001t0113g0151 a0001c0002t0001g0075 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3297+349T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125004916 | |||||||
chr3:125005178 | A | C | 5 | a0013c0017t0028g0282 a0013c0017t0041g0153 a0013c0017t0096g0049 others(2): Show |
5 | HG00323.hp2 HG01255.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.3297+87T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 9/16 | chr3 | 125005178 | |||||||
chr3:125005739 | T | C | 8 | a0005c0086t0090g0085 a0021c0023t0031g0183 a0021c0023t0031g0190 others(5): Show |
8 | HG02258.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3194-371A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005739 | |||||||
chr3:125005890 | T | C | 2 | a0005c0006t0002g0179 a0008c0009t0138g0346 |
2 | HG00735.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.3194-522A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005890 | |||||||
chr3:125005979 | G | A | 125 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(122): Show |
128 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.3194-611C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005979 | |||||||
chr3:125005990 | A | C | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-622T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125005990 | |||||||
chr3:125006016 | G | T | 1 | a0004c0042t0134g0343 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3194-648C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006016 | |||||||
chr3:125006100 | A | T | 1 | a0007c0060t0139g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3194-732T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006100 | |||||||
chr3:125006260 | C | A | 5 | a0001c0001t0070g0195 a0002c0082t0069g0193 a0019c0026t0053g0302 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3194-892G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006260 | |||||||
chr3:125006432 | G | A | 1 | a0001c0020t0041g0019 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3194-1064C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006432 | |||||||
chr3:125006452 | A | G | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-1084T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006452 | |||||||
chr3:125006691 | G | A | 1 | a0037c0050t0022g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3194-1323C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006691 | |||||||
chr3:125006815 | C | A | 185 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(182): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.3194-1447G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006815 | |||||||
chr3:125006871 | G | C | 1 | a0002c0005t0004g0276 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3194-1503C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006871 | |||||||
chr3:125006938 | G | A | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-1570C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006938 | |||||||
chr3:125006943 | T | C | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3194-1575A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125006943 | |||||||
chr3:125007026 | C | T | 1 | a0002c0005t0010g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3194-1658G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007026 | |||||||
chr3:125007133 | A | G | 55 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(52): Show |
57 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(54): Show |
intron_variant | MODIFIER | c.3194-1765T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007133 | |||||||
chr3:125007198 | C | CA | 72 | a0001c0001t0018g0252 a0001c0001t0047g0123 a0001c0001t0059g0260 others(69): Show |
76 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.3194-1831dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007198 | |||||||
chr3:125007198 | C | CAA | 8 | a0002c0081t0116g0244 a0004c0038t0131g0301 a0006c0077t0073g0088 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3194-1832_3194-183 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007198 | |||||||
chr3:125007198 | CA | C | 8 | a0001c0001t0004g0293 a0001c0001t0027g0279 a0001c0001t0092g0188 others(5): Show |
8 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3194-1831delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007198 | |||||||
chr3:125007455 | T | C | 8 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 others(5): Show |
8 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3194-2087A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007455 | |||||||
chr3:125007747 | A | G | 258 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(255): Show |
264 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.3193+1958T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007747 | |||||||
chr3:125007861 | G | A | 105 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(102): Show |
106 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.3193+1844C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125007861 | |||||||
chr3:125008464 | A | C | 1 | a0001c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3193+1241T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008464 | |||||||
chr3:125008580 | C | G | 12 | a0001c0001t0126g0272 a0001c0001t0127g0299 a0006c0011t0022g0003 others(9): Show |
14 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3193+1125G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008580 | |||||||
chr3:125008712 | G | A | 1 | a0018c0037t0109g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3193+993C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008712 | |||||||
chr3:125008814 | AAAAACAC | A | 258 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(255): Show |
264 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.3193+884_3193+890d others(9): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008814 | |||||||
chr3:125008821 | C | A | 1 | a0004c0038t0013g0322 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3193+884G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008821 | |||||||
chr3:125008903 | A | G | 203 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(200): Show |
207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.3193+802T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008903 | |||||||
chr3:125008934 | C | T | 184 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(181): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.3193+771G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125008934 | |||||||
chr3:125009215 | T | A | 1 | a0003c0004t0002g0172 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3193+490A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009215 | |||||||
chr3:125009216 | A | C | 1 | a0037c0050t0022g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3193+489T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009216 | |||||||
chr3:125009249 | A | AATC | 56 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(53): Show |
58 | HG00597.hp2 HG00733.hp1 HG01433.hp2 others(55): Show |
intron_variant | MODIFIER | c.3193+453_3193+455d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009249 | |||||||
chr3:125009286 | G | GT | 15 | a0001c0002t0016g0047 a0001c0002t0033g0051 a0004c0007t0125g0344 others(12): Show |
17 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3193+418dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009286 | |||||||
chr3:125009401 | G | A | 1 | a0001c0002t0016g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3193+304C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009401 | |||||||
chr3:125009550 | T | C | 259 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.3193+155A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009550 | |||||||
chr3:125009628 | C | G | 203 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(200): Show |
207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.3193+77G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009628 | |||||||
chr3:125009671 | C | T | 1 | a0003c0067t0019g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3193+34G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 8/16 | chr3 | 125009671 | |||||||
chr3:125009964 | C | A | 54 | a0002c0003t0007g0070 a0002c0003t0007g0071 a0002c0003t0007g0077 others(51): Show |
56 | HG00597.hp2 HG01433.hp2 HG01891.hp2 others(53): Show |
intron_variant | MODIFIER | c.3074-140G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125009964 | |||||||
chr3:125010048 | G | T | 1 | a0001c0001t0098g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3074-224C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010048 | |||||||
chr3:125010067 | A | G | 2 | a0028c0090t0119g0348 a0029c0075t0076g0182 |
2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.3074-243T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010067 | |||||||
chr3:125010160 | C | T | 4 | a0011c0041t0035g0309 a0011c0041t0035g0311 a0038c0079t0079g0181 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3073+279G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010160 | |||||||
chr3:125010228 | G | C | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3073+211C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010228 | |||||||
chr3:125010253 | G | T | 258 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.3073+186C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010253 | |||||||
chr3:125010258 | G | C | 167 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0012g0173 others(164): Show |
169 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.3073+181C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010258 | |||||||
chr3:125010349 | T | G | 151 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0012g0173 others(148): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.3073+90A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010349 | |||||||
chr3:125010397 | G | A | 2 | a0002c0082t0069g0193 a0007c0060t0139g0217 |
2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3073+42C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 7/16 | chr3 | 125010397 | |||||||
chr3:125010666 | T | C | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2957-111A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010666 | |||||||
chr3:125010680 | A | T | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2957-125T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010680 | |||||||
chr3:125010874 | C | G | 1 | a0005c0006t0022g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2957-319G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010874 | |||||||
chr3:125010990 | C | T | 1 | a0001c0002t0005g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2957-435G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125010990 | |||||||
chr3:125011245 | C | CA | 99 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(96): Show |
104 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2957-691dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011245 | |||||||
chr3:125011245 | C | CAA | 11 | a0002c0003t0082g0185 a0002c0071t0083g0186 a0004c0007t0013g0305 others(8): Show |
11 | HG01243.hp1 HG01346.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.2957-692_2957-691d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011245 | |||||||
chr3:125011245 | CA | C | 7 | a0001c0001t0059g0260 a0001c0002t0024g0116 a0005c0006t0022g0089 others(4): Show |
7 | HG01891.hp2 HG02148.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2957-691delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011245 | |||||||
chr3:125011288 | T | C | 110 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(107): Show |
115 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2957-733A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011288 | |||||||
chr3:125011408 | C | T | 5 | a0006c0011t0010g0194 a0006c0011t0022g0003 a0006c0011t0086g0081 others(2): Show |
6 | HG01109.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957-853G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011408 | |||||||
chr3:125011441 | A | T | 166 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2957-886T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011441 | |||||||
chr3:125011597 | G | T | 1 | a0004c0040t0059g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2956+1026C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011597 | |||||||
chr3:125011715 | G | T | 1 | a0002c0071t0083g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2956+908C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011715 | |||||||
chr3:125011770 | C | T | 1 | a0001c0001t0027g0279 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2956+853G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125011770 | |||||||
chr3:125012081 | C | G | 174 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(171): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2956+542G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012081 | |||||||
chr3:125012095 | C | T | 1 | a0008c0009t0004g0328 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2956+528G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012095 | |||||||
chr3:125012129 | C | T | 1 | a0002c0028t0080g0029 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2956+494G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012129 | |||||||
chr3:125012228 | T | A | 293 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2956+395A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012228 | |||||||
chr3:125012237 | TCTTTA | T | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2956+381_2956+385d others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 6/16 | chr3 | 125012237 | |||||||
chr3:125013998 | C | A | 269 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(266): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
splice_region_variant&intron_variant | LOW | c.1589-8G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125013998 | |||||||
chr3:125014018 | C | G | 7 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0018c0088t0010g0178 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1589-28G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014018 | |||||||
chr3:125014132 | G | T | 279 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(276): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1589-142C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014132 | |||||||
chr3:125014133 | G | T | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1589-143C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014133 | |||||||
chr3:125014153 | ACAT | A | 3 | a0019c0026t0053g0302 a0019c0026t0053g0303 a0019c0026t0117g0304 |
3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1589-166_1589-164d others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014153 | |||||||
chr3:125014377 | T | C | 1 | a0002c0005t0043g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1589-387A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014377 | |||||||
chr3:125014510 | G | A | 2 | a0028c0090t0119g0348 a0029c0075t0076g0182 |
2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1589-520C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014510 | |||||||
chr3:125014512 | G | A | 1 | a0001c0001t0099g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1589-522C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014512 | |||||||
chr3:125014523 | G | C | 2 | a0002c0082t0069g0193 a0007c0060t0139g0217 |
2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1589-533C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014523 | |||||||
chr3:125014641 | T | A | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-651A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014641 | |||||||
chr3:125014650 | G | T | 336 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(333): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1589-660C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014650 | |||||||
chr3:125014655 | G | A | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1589-665C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014655 | |||||||
chr3:125014682 | G | A | 2 | a0004c0042t0004g0347 a0004c0042t0134g0343 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1589-692C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014682 | |||||||
chr3:125014769 | A | C | 1 | a0002c0003t0006g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1589-779T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014769 | |||||||
chr3:125014805 | T | G | 293 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1589-815A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014805 | |||||||
chr3:125014927 | G | C | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1589-937C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125014927 | |||||||
chr3:125015024 | G | A | 3 | a0011c0041t0035g0309 a0011c0041t0035g0311 a0042c0091t0122g0310 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1589-1034C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015024 | |||||||
chr3:125015108 | C | T | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1589-1118G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015108 | |||||||
chr3:125015482 | C | T | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1589-1492G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015482 | |||||||
chr3:125015609 | C | T | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1589-1619G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015609 | |||||||
chr3:125015649 | T | G | 3 | a0001c0001t0059g0260 a0005c0006t0088g0066 a0030c0080t0085g0087 |
3 | HG01891.hp2 HG02148.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1589-1659A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015649 | |||||||
chr3:125015702 | T | A | 4 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0028c0090t0119g0348 others(1): Show |
5 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589-1712A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015702 | |||||||
chr3:125015733 | T | C | 1 | a0002c0003t0015g0072 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1589-1743A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015733 | |||||||
chr3:125015792 | A | G | 4 | a0001c0002t0001g0092 a0001c0002t0024g0093 a0001c0002t0024g0094 others(1): Show |
4 | HG00140.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589-1802T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015792 | |||||||
chr3:125015801 | C | A | 188 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(185): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1589-1811G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015801 | |||||||
chr3:125015802 | C | A | 162 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1589-1812G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015802 | |||||||
chr3:125015966 | C | T | 287 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(284): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1589-1976G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015966 | |||||||
chr3:125015979 | T | C | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1589-1989A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015979 | |||||||
chr3:125015980 | C | A | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1589-1990G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125015980 | |||||||
chr3:125016091 | T | C | 4 | a0001c0001t0059g0260 a0005c0006t0022g0089 a0005c0006t0088g0066 others(1): Show |
4 | HG01891.hp2 HG02148.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1589-2101A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016091 | |||||||
chr3:125016314 | A | C | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1589-2324T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016314 | |||||||
chr3:125016438 | C | T | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-2448G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016438 | |||||||
chr3:125016471 | G | A | 4 | a0010c0008t0004g0236 a0010c0008t0036g0238 a0010c0008t0036g0239 others(1): Show |
4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589-2481C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016471 | |||||||
chr3:125016625 | C | T | 9 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0093g0163 others(6): Show |
9 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1589-2635G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016625 | |||||||
chr3:125016627 | T | C | 188 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(185): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1588+2635A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016627 | |||||||
chr3:125016628 | G | A | 10 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 others(7): Show |
10 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588+2634C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016628 | |||||||
chr3:125016787 | T | C | 3 | a0002c0033t0023g0164 a0002c0044t0023g0016 a0004c0089t0026g0306 |
3 | HG03195.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1588+2475A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016787 | |||||||
chr3:125016788 | G | A | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1588+2474C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125016788 | |||||||
chr3:125017059 | CT | C | 211 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1588+2202delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017059 | |||||||
chr3:125017120 | T | A | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1588+2142A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017120 | |||||||
chr3:125017141 | A | G | 287 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(284): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1588+2121T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017141 | |||||||
chr3:125017201 | C | T | 1 | a0001c0002t0051g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1588+2061G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017201 | |||||||
chr3:125017301 | C | T | 7 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0018c0088t0010g0178 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1961G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017301 | |||||||
chr3:125017406 | T | C | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1856A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017406 | |||||||
chr3:125017529 | C | T | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1588+1733G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017529 | |||||||
chr3:125017530 | C | T | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1732G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017530 | |||||||
chr3:125017534 | C | T | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1728G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017534 | |||||||
chr3:125017661 | C | T | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1601G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017661 | |||||||
chr3:125017747 | A | G | 276 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1588+1515T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017747 | |||||||
chr3:125017864 | T | TA | 25 | a0001c0001t0007g0114 a0001c0002t0001g0075 a0001c0002t0001g0080 others(22): Show |
25 | HG00099.hp2 HG01167.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1588+1397dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017864 | |||||||
chr3:125017946 | G | A | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1316C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125017946 | |||||||
chr3:125018010 | C | T | 2 | a0001c0002t0016g0047 a0001c0002t0033g0046 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1588+1252G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018010 | |||||||
chr3:125018028 | C | CA | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1588+1233dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018028 | |||||||
chr3:125018037 | A | T | 75 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(72): Show |
78 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1588+1225T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018037 | |||||||
chr3:125018042 | T | A | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1588+1220A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018042 | |||||||
chr3:125018142 | A | T | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1588+1120T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018142 | |||||||
chr3:125018195 | T | C | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588+1067A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018195 | |||||||
chr3:125018282 | T | C | 3 | a0011c0041t0035g0309 a0011c0041t0035g0311 a0042c0091t0122g0310 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1588+980A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018282 | |||||||
chr3:125018454 | C | T | 1 | a0004c0040t0059g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1588+808G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018454 | |||||||
chr3:125018585 | C | T | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1588+677G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018585 | |||||||
chr3:125018820 | G | C | 1 | a0046c0063t0005g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1588+442C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018820 | |||||||
chr3:125018864 | C | CT | 15 | a0001c0001t0018g0252 a0001c0002t0001g0143 a0002c0003t0006g0265 others(12): Show |
15 | HG00639.hp1 HG01255.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1588+397dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018864 | |||||||
chr3:125018864 | CT | C | 18 | a0001c0001t0004g0274 a0002c0005t0012g0158 a0002c0071t0083g0186 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1588+397delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018864 | |||||||
chr3:125018959 | T | C | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1588+303A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018959 | |||||||
chr3:125018968 | A | C | 3 | a0019c0026t0053g0302 a0019c0026t0053g0303 a0019c0026t0117g0304 |
3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1588+294T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125018968 | |||||||
chr3:125019040 | G | A | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1588+222C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019040 | |||||||
chr3:125019049 | G | T | 1 | a0009c0022t0008g0231 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1588+213C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019049 | |||||||
chr3:125019069 | T | C | 4 | a0001c0002t0016g0052 a0001c0002t0033g0051 a0009c0016t0141g0223 others(1): Show |
4 | NA18955.hp2 NA18989.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1588+193A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019069 | |||||||
chr3:125019187 | C | T | 2 | a0001c0001t0097g0145 a0006c0015t0005g0285 |
2 | HG00597.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1588+75G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019187 | |||||||
chr3:125019205 | C | A | 1 | a0002c0003t0006g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1588+57G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019205 | |||||||
chr3:125019228 | A | G | 1 | a0001c0002t0005g0286 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1588+34T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 5/16 | chr3 | 125019228 | |||||||
chr3:125019860 | C | T | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1253-263G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125019860 | |||||||
chr3:125020020 | A | G | 7 | a0006c0077t0073g0088 a0011c0041t0035g0309 a0011c0041t0035g0311 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1253-423T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020020 | |||||||
chr3:125020074 | T | A | 1 | a0001c0002t0033g0051 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1253-477A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020074 | |||||||
chr3:125020164 | T | C | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253-567A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020164 | |||||||
chr3:125020290 | G | C | 170 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1252+502C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020290 | |||||||
chr3:125020775 | A | G | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1252+17T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 4/16 | chr3 | 125020775 | |||||||
chr3:125021160 | T | A | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-30A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021160 | |||||||
chr3:125021611 | G | A | 187 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.914-481C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021611 | |||||||
chr3:125021694 | G | C | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.914-564C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021694 | |||||||
chr3:125021960 | T | C | 1 | a0013c0017t0045g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.914-830A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125021960 | |||||||
chr3:125022010 | C | T | 2 | a0005c0006t0022g0089 a0047c0078t0015g0156 |
2 | HG03098.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.914-880G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022010 | |||||||
chr3:125022015 | T | C | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-885A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022015 | |||||||
chr3:125022049 | C | T | 1 | a0001c0002t0001g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.914-919G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022049 | |||||||
chr3:125022227 | G | A | 86 | a0001c0001t0007g0114 a0001c0001t0044g0161 a0001c0001t0097g0145 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.914-1097C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022227 | |||||||
chr3:125022396 | C | CGA | 23 | a0001c0001t0047g0123 a0001c0002t0033g0051 a0002c0003t0082g0185 others(20): Show |
23 | HG00140.hp2 HG01346.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.914-1268_914-1267d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | C | CGAGA | 137 | a0001c0001t0006g0281 a0001c0001t0007g0114 a0001c0001t0008g0242 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.914-1270_914-1267d others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | C | CGAGAGA | 30 | a0001c0001t0006g0280 a0001c0001t0018g0251 a0001c0001t0042g0098 others(27): Show |
31 | HG00323.hp2 HG00609.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.914-1272_914-1267d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | C | CGAGAGAG others(1): Show |
8 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0277 others(5): Show |
8 | HG01255.hp1 HG03139.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-1274_914-1267d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | C | CGAGAGAG others(3): Show |
5 | a0001c0001t0004g0275 a0026c0059t0058g0220 a0027c0046t0019g0024 others(2): Show |
5 | HG00639.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-1276_914-1267d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | C | CGAGAGAG others(5): Show |
1 | a0027c0047t0108g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.914-1278_914-1267d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | C | CGAGAGAG others(7): Show |
2 | a0026c0058t0057g0219 a0035c0066t0068g0011 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.914-1280_914-1267d others(16): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022396 | CGA | C | 4 | a0019c0026t0053g0302 a0019c0026t0053g0303 a0019c0026t0117g0304 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-1268_914-1267d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022396 | |||||||
chr3:125022428 | T | A | 187 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.914-1298A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022428 | |||||||
chr3:125022454 | C | G | 2 | a0001c0002t0016g0047 a0001c0002t0033g0046 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.914-1324G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022454 | |||||||
chr3:125022554 | A | G | 1 | a0021c0023t0031g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.914-1424T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022554 | |||||||
chr3:125022612 | G | A | 76 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(73): Show |
79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.914-1482C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022612 | |||||||
chr3:125022653 | T | C | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.914-1523A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022653 | |||||||
chr3:125022693 | AAAGAAAT | A | 16 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(13): Show |
16 | HG00323.hp1 HG00735.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.914-1570_914-1564d others(9): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022693 | |||||||
chr3:125022694 | AAGAAAT | A | 154 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0007g0114 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.914-1570_914-1565d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022694 | |||||||
chr3:125022694 | AAGAAATA others(3): Show |
A | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-1574_914-1565d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022694 | |||||||
chr3:125022704 | T | G | 170 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.914-1574A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022704 | |||||||
chr3:125022707 | AT | A | 4 | a0001c0010t0001g0023 a0009c0016t0005g0221 a0025c0036t0030g0068 others(1): Show |
4 | HG02083.hp2 HG02132.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-1578delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022707 | |||||||
chr3:125022708 | T | G | 173 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.914-1578A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022708 | |||||||
chr3:125022709 | A | G | 4 | a0001c0010t0001g0023 a0009c0016t0005g0221 a0025c0036t0030g0068 others(1): Show |
4 | HG02083.hp2 HG02132.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-1579T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022709 | |||||||
chr3:125022713 | AG | A | 173 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.914-1584delC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022713 | |||||||
chr3:125022876 | T | G | 1 | a0001c0001t0127g0299 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.914-1746A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022876 | |||||||
chr3:125022915 | C | T | 1 | a0012c0019t0001g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.914-1785G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125022915 | |||||||
chr3:125023051 | G | A | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-1921C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023051 | |||||||
chr3:125023079 | A | G | 1 | a0013c0017t0045g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.914-1949T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023079 | |||||||
chr3:125023125 | T | C | 2 | a0034c0061t0035g0222 a0044c0084t0019g0086 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.914-1995A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023125 | |||||||
chr3:125023158 | T | C | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.914-2028A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023158 | |||||||
chr3:125023238 | C | CA | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.914-2109dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023238 | |||||||
chr3:125023479 | A | G | 1 | a0002c0003t0006g0284 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.914-2349T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023479 | |||||||
chr3:125023510 | G | A | 276 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.914-2380C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023510 | |||||||
chr3:125023665 | T | TA | 187 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.914-2536_914-2535i others(3): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023665 | |||||||
chr3:125023746 | C | T | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.914-2616G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023746 | |||||||
chr3:125023766 | C | T | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.914-2636G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023766 | |||||||
chr3:125023972 | C | CTGA | 187 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.914-2843_914-2842i others(5): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125023972 | |||||||
chr3:125024041 | A | G | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-2911T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024041 | |||||||
chr3:125024124 | T | C | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.914-2994A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024124 | |||||||
chr3:125024135 | T | A | 2 | a0002c0082t0069g0193 a0007c0060t0139g0217 |
2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.914-3005A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024135 | |||||||
chr3:125024179 | T | A | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.913+3026A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024179 | |||||||
chr3:125024626 | C | G | 170 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.913+2579G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024626 | |||||||
chr3:125024729 | G | A | 2 | a0005c0006t0003g0112 a0005c0006t0019g0111 |
2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.913+2476C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024729 | |||||||
chr3:125024759 | G | A | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.913+2446C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024759 | |||||||
chr3:125024868 | C | T | 180 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.913+2337G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024868 | |||||||
chr3:125024869 | T | C | 180 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.913+2336A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024869 | |||||||
chr3:125024944 | G | A | 1 | a0004c0007t0129g0345 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.913+2261C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125024944 | |||||||
chr3:125025119 | G | A | 7 | a0018c0037t0063g0254 a0018c0037t0109g0187 a0018c0088t0010g0178 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+2086C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025119 | |||||||
chr3:125025200 | C | A | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.913+2005G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025200 | |||||||
chr3:125025450 | G | A | 4 | a0002c0033t0023g0164 a0002c0033t0094g0165 a0002c0044t0023g0016 others(1): Show |
4 | HG03195.hp2 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+1755C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025450 | |||||||
chr3:125025494 | A | G | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.913+1711T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025494 | |||||||
chr3:125025561 | C | G | 274 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.913+1644G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025561 | |||||||
chr3:125025764 | C | T | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+1441G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025764 | |||||||
chr3:125025839 | C | A | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.913+1366G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025839 | |||||||
chr3:125025922 | G | C | 3 | a0019c0026t0053g0302 a0019c0026t0053g0303 a0019c0026t0117g0304 |
3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.913+1283C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125025922 | |||||||
chr3:125026198 | T | G | 5 | a0006c0011t0010g0194 a0006c0011t0022g0003 a0006c0011t0086g0081 others(2): Show |
6 | HG01109.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.913+1007A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026198 | |||||||
chr3:125026287 | C | T | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.913+918G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026287 | |||||||
chr3:125026627 | A | G | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.913+578T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026627 | |||||||
chr3:125026874 | C | T | 1 | a0015c0057t0128g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.913+331G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026874 | |||||||
chr3:125026937 | T | C | 1 | a0001c0001t0077g0044 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.913+268A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125026937 | |||||||
chr3:125027030 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.913+175A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 3/16 | chr3 | 125027030 | |||||||
chr3:125027538 | A | G | 1 | a0001c0002t0016g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.611-31T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027538 | |||||||
chr3:125027737 | C | A | 2 | a0028c0090t0119g0348 a0029c0075t0076g0182 |
2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.611-230G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027737 | |||||||
chr3:125027836 | C | A | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.611-329G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027836 | |||||||
chr3:125027930 | T | C | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.611-423A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125027930 | |||||||
chr3:125028024 | TCTGACGG others(69): Show |
T | 1 | a0002c0005t0009g0078 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-593_611-518del others(76): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028024 | |||||||
chr3:125028214 | G | A | 1 | a0001c0010t0107g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.611-707C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028214 | |||||||
chr3:125028338 | G | A | 13 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.611-831C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028338 | |||||||
chr3:125028435 | C | A | 13 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+760G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028435 | |||||||
chr3:125028517 | C | A | 3 | a0002c0005t0027g0258 a0002c0005t0028g0257 a0002c0005t0028g0259 |
3 | NA18999.hp2 NA19062.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.610+678G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028517 | |||||||
chr3:125028524 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.610+671G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125028524 | |||||||
chr3:125029173 | C | T | 1 | a0002c0003t0007g0070 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.610+22G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 2/16 | chr3 | 125029173 | |||||||
chr3:125029653 | G | T | 1 | a0021c0023t0031g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.317-165C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029653 | |||||||
chr3:125029708 | G | A | 1 | a0001c0001t0101g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.317-220C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029708 | |||||||
chr3:125029749 | G | A | 1 | a0008c0009t0061g0319 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.317-261C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029749 | |||||||
chr3:125029792 | T | C | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-304A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029792 | |||||||
chr3:125029835 | T | C | 1 | a0002c0005t0042g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.317-347A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029835 | |||||||
chr3:125029846 | C | T | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.317-358G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029846 | |||||||
chr3:125029865 | C | A | 1 | a0002c0005t0004g0276 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.317-377G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029865 | |||||||
chr3:125029945 | T | G | 3 | a0011c0041t0035g0309 a0011c0041t0035g0311 a0042c0091t0122g0310 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.317-457A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125029945 | |||||||
chr3:125030115 | T | C | 1 | a0013c0017t0045g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.317-627A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030115 | |||||||
chr3:125030201 | T | C | 1 | a0005c0006t0118g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.317-713A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030201 | |||||||
chr3:125030432 | G | A | 188 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(185): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.317-944C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030432 | |||||||
chr3:125030522 | A | T | 5 | a0003c0004t0014g0283 a0003c0004t0040g0175 a0003c0004t0040g0176 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-1034T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030522 | |||||||
chr3:125030619 | G | GA | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-1132dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030619 | |||||||
chr3:125030647 | T | C | 60 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(57): Show |
61 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.317-1159A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030647 | |||||||
chr3:125030712 | C | T | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-1224G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030712 | |||||||
chr3:125030740 | T | C | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-1252A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030740 | |||||||
chr3:125030956 | C | T | 189 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.317-1468G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125030956 | |||||||
chr3:125031127 | G | A | 273 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.317-1639C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031127 | |||||||
chr3:125031160 | G | A | 2 | a0028c0090t0119g0348 a0029c0075t0076g0182 |
2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.317-1672C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031160 | |||||||
chr3:125031164 | C | T | 9 | a0006c0011t0011g0061 a0006c0011t0011g0125 a0010c0008t0004g0236 others(6): Show |
9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.317-1676G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031164 | |||||||
chr3:125031182 | C | T | 2 | a0005c0006t0022g0089 a0038c0079t0079g0181 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-1694G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031182 | |||||||
chr3:125031306 | G | T | 13 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.317-1818C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031306 | |||||||
chr3:125031531 | C | A | 8 | a0002c0003t0003g0004 a0002c0003t0003g0005 a0002c0003t0003g0006 others(5): Show |
11 | HG00544.hp2 HG00673.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.317-2043G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031531 | |||||||
chr3:125031572 | G | T | 11 | a0002c0003t0082g0185 a0002c0071t0083g0186 a0004c0007t0013g0305 others(8): Show |
11 | HG01243.hp1 HG01346.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.317-2084C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031572 | |||||||
chr3:125031653 | CCA | C | 7 | a0005c0006t0022g0089 a0021c0023t0031g0183 a0021c0023t0031g0190 others(4): Show |
7 | HG02486.hp2 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-2167_317-2166d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031653 | |||||||
chr3:125031680 | TAC | T | 76 | a0001c0010t0001g0014 a0002c0003t0002g0157 a0002c0003t0003g0004 others(73): Show |
79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.317-2194_317-2193d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031680 | |||||||
chr3:125031687 | A | C | 4 | a0005c0006t0022g0089 a0034c0061t0035g0222 a0038c0079t0079g0181 others(1): Show |
4 | HG02486.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-2199T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031687 | |||||||
chr3:125031703 | A | AC | 7 | a0005c0006t0022g0089 a0021c0023t0031g0183 a0021c0023t0031g0190 others(4): Show |
7 | HG02486.hp2 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-2216dupG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031703 | |||||||
chr3:125031703 | AC | A | 172 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.317-2216delG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031703 | |||||||
chr3:125031710 | A | C | 3 | a0005c0006t0022g0089 a0006c0077t0073g0088 a0038c0079t0079g0181 |
3 | HG02572.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-2222T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031710 | |||||||
chr3:125031830 | A | G | 176 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(173): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.317-2342T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031830 | |||||||
chr3:125031832 | G | A | 176 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(173): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.317-2344C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031832 | |||||||
chr3:125031849 | C | T | 2 | a0034c0061t0035g0222 a0044c0084t0019g0086 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-2361G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125031849 | |||||||
chr3:125032137 | C | A | 2 | a0001c0001t0044g0104 a0001c0001t0100g0096 |
2 | HG01243.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.317-2649G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032137 | |||||||
chr3:125032137 | C | T | 2 | a0034c0061t0035g0222 a0044c0084t0019g0086 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-2649G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032137 | |||||||
chr3:125032153 | G | A | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-2665C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032153 | |||||||
chr3:125032421 | G | A | 1 | a0047c0078t0015g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.317-2933C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032421 | |||||||
chr3:125032484 | C | T | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-2996G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032484 | |||||||
chr3:125032808 | C | T | 2 | a0001c0002t0016g0062 a0001c0010t0001g0026 |
2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.317-3320G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032808 | |||||||
chr3:125032868 | C | A | 2 | a0002c0003t0089g0126 a0007c0013t0004g0211 |
2 | NA18974.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.317-3380G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032868 | |||||||
chr3:125032966 | G | A | 4 | a0010c0008t0004g0236 a0010c0008t0036g0238 a0010c0008t0036g0239 others(1): Show |
4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-3478C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125032966 | |||||||
chr3:125033014 | G | A | 1 | a0002c0005t0009g0078 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.317-3526C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033014 | |||||||
chr3:125033160 | A | T | 1 | a0001c0001t0101g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.317-3672T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033160 | |||||||
chr3:125033226 | G | A | 1 | a0020c0096t0006g0341 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.317-3738C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033226 | |||||||
chr3:125033293 | T | C | 1 | a0007c0013t0124g0232 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.317-3805A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033293 | |||||||
chr3:125033304 | T | A | 2 | a0005c0006t0022g0089 a0038c0079t0079g0181 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-3816A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033304 | |||||||
chr3:125033734 | G | A | 6 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-4246C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033734 | |||||||
chr3:125033777 | G | A | 2 | a0002c0003t0003g0006 a0002c0003t0003g0107 |
3 | NA18944.hp2 NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.317-4289C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033777 | |||||||
chr3:125033834 | G | A | 1 | a0003c0004t0021g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.317-4346C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033834 | |||||||
chr3:125033892 | GC | G | 3 | a0001c0002t0001g0075 a0001c0002t0001g0080 a0009c0016t0038g0218 |
3 | NA18942.hp2 NA18970.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.317-4405delG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033892 | |||||||
chr3:125033899 | C | G | 4 | a0005c0006t0022g0089 a0034c0061t0035g0222 a0038c0079t0079g0181 others(1): Show |
4 | HG02486.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-4411G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033899 | |||||||
chr3:125033910 | T | A | 174 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.317-4422A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033910 | |||||||
chr3:125033953 | C | T | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.317-4465G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033953 | |||||||
chr3:125033961 | C | T | 1 | a0001c0001t0011g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.317-4473G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033961 | |||||||
chr3:125033972 | C | T | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-4484G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125033972 | |||||||
chr3:125034027 | G | A | 88 | a0001c0002t0016g0062 a0001c0010t0001g0014 a0001c0010t0001g0026 others(85): Show |
92 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.317-4539C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034027 | |||||||
chr3:125034082 | T | C | 177 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.317-4594A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034082 | |||||||
chr3:125034083 | G | C | 1 | a0001c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.317-4595C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034083 | |||||||
chr3:125034084 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.317-4596C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034084 | |||||||
chr3:125034094 | G | A | 1 | a0008c0009t0011g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.317-4606C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034094 | |||||||
chr3:125034136 | C | T | 1 | a0021c0023t0031g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.317-4648G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034136 | |||||||
chr3:125034172 | A | C | 1 | a0002c0003t0007g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.317-4684T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034172 | |||||||
chr3:125034184 | A | G | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-4696T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034184 | |||||||
chr3:125034192 | T | TTGATAAC others(43): Show |
178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-4705_317-4704i others(52): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034192 | |||||||
chr3:125034250 | T | C | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-4762A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034250 | |||||||
chr3:125034349 | T | C | 182 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.317-4861A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034349 | |||||||
chr3:125034362 | A | T | 2 | a0034c0061t0035g0222 a0044c0084t0019g0086 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-4874T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034362 | |||||||
chr3:125034363 | T | A | 1 | a0005c0006t0009g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.317-4875A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034363 | |||||||
chr3:125034428 | A | G | 2 | a0034c0061t0035g0222 a0044c0084t0019g0086 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-4940T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034428 | |||||||
chr3:125034433 | TA | T | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-4946delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034433 | |||||||
chr3:125034470 | A | G | 182 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.317-4982T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034470 | |||||||
chr3:125034538 | C | T | 2 | a0002c0082t0069g0193 a0007c0060t0139g0217 |
2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.317-5050G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034538 | |||||||
chr3:125034676 | G | A | 3 | a0008c0009t0018g0337 a0034c0061t0035g0222 a0044c0084t0019g0086 |
3 | HG02486.hp2 HG03471.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.317-5188C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034676 | |||||||
chr3:125034690 | C | T | 5 | a0026c0058t0057g0219 a0026c0059t0058g0220 a0027c0046t0019g0024 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-5202G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034690 | |||||||
chr3:125034692 | T | C | 1 | a0003c0067t0019g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.317-5204A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034692 | |||||||
chr3:125034922 | T | C | 4 | a0003c0004t0009g0073 a0015c0021t0006g0215 a0015c0021t0006g0216 others(1): Show |
4 | NA18988.hp2 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-5434A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034922 | |||||||
chr3:125034977 | T | C | 2 | a0005c0006t0022g0089 a0038c0079t0079g0181 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.317-5489A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125034977 | |||||||
chr3:125035081 | C | G | 3 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0007c0060t0139g0217 |
3 | HG01891.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.317-5593G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035081 | |||||||
chr3:125035099 | A | G | 273 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.317-5611T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035099 | |||||||
chr3:125035250 | T | G | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5762A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035250 | |||||||
chr3:125035251 | A | C | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5763T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035251 | |||||||
chr3:125035252 | A | T | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5764T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035252 | |||||||
chr3:125035255 | T | C | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5767A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035255 | |||||||
chr3:125035256 | T | A | 1 | a0043c0092t0133g0314 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.317-5768A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035256 | |||||||
chr3:125035268 | T | TG | 90 | a0001c0001t0007g0114 a0001c0001t0044g0161 a0001c0001t0097g0145 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.317-5781dupC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035268 | |||||||
chr3:125035318 | G | T | 178 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.317-5830C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035318 | |||||||
chr3:125035421 | A | G | 1 | a0004c0007t0025g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.317-5933T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035421 | |||||||
chr3:125035464 | A | T | 1 | a0012c0030t0048g0037 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.317-5976T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035464 | |||||||
chr3:125035580 | C | T | 1 | a0002c0033t0023g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.317-6092G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035580 | |||||||
chr3:125035596 | C | T | 2 | a0002c0003t0007g0083 a0002c0003t0015g0084 |
2 | HG03654.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.317-6108G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035596 | |||||||
chr3:125035729 | T | A | 3 | a0005c0006t0002g0179 a0005c0006t0054g0247 a0008c0009t0138g0346 |
3 | HG00323.hp1 HG00735.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.317-6241A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035729 | |||||||
chr3:125035807 | G | A | 1 | a0012c0019t0001g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.317-6319C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125035807 | |||||||
chr3:125036209 | C | CAAAAAA | 47 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0059g0260 others(44): Show |
48 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.317-6727_317-6722d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036209 | C | CAAAAAAA | 123 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.317-6728_317-6722d others(9): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036209 | C | CAAAAAAA others(1): Show |
6 | a0001c0002t0001g0092 a0001c0002t0001g0143 a0001c0002t0001g0144 others(3): Show |
6 | HG00733.hp1 HG02155.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-6729_317-6722d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036209 | C | CAAAAAAA others(4): Show |
1 | a0004c0007t0123g0349 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.317-6732_317-6722d others(13): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036209 | C | CAAAAAAA others(5): Show |
76 | a0001c0002t0016g0062 a0001c0010t0001g0014 a0001c0010t0001g0026 others(73): Show |
79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.317-6733_317-6722d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036209 | C | CAAAAAAA others(6): Show |
9 | a0002c0005t0004g0276 a0002c0005t0027g0258 a0002c0049t0087g0030 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-6734_317-6722d others(15): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036209 | C | CAAAAAAA others(7): Show |
1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.317-6735_317-6722d others(16): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036209 | |||||||
chr3:125036213 | A | AAAAAAAA others(5): Show |
3 | a0016c0025t0025g0009 a0016c0025t0130g0316 a0036c0069t0111g0202 |
4 | HG00735.hp2 HG01074.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-6726_317-6725i others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036213 | |||||||
chr3:125036299 | C | T | 6 | a0001c0001t0008g0242 a0001c0001t0008g0246 a0001c0001t0029g0154 others(3): Show |
6 | HG00639.hp2 HG01081.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-6811G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036299 | |||||||
chr3:125036326 | A | T | 1 | a0014c0053t0001g0034 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.317-6838T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036326 | |||||||
chr3:125036381 | C | T | 76 | a0001c0002t0016g0062 a0001c0010t0001g0014 a0001c0010t0001g0026 others(73): Show |
79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.317-6893G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036381 | |||||||
chr3:125036391 | C | T | 1 | a0002c0028t0080g0029 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.317-6903G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036391 | |||||||
chr3:125036604 | A | G | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-7116T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036604 | |||||||
chr3:125036642 | T | C | 180 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.317-7154A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036642 | |||||||
chr3:125036832 | T | C | 2 | a0034c0061t0035g0222 a0044c0084t0019g0086 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.317-7344A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036832 | |||||||
chr3:125036854 | T | C | 3 | a0001c0001t0044g0104 a0001c0001t0100g0096 a0008c0009t0138g0346 |
3 | HG01243.hp2 HG01256.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.317-7366A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036854 | |||||||
chr3:125036950 | A | G | 7 | a0002c0081t0116g0244 a0002c0082t0069g0193 a0004c0042t0004g0347 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-7462T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036950 | |||||||
chr3:125036979 | G | A | 1 | a0036c0069t0111g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.317-7491C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036979 | |||||||
chr3:125036979 | G | T | 175 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(172): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.317-7491C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125036979 | |||||||
chr3:125037125 | T | C | 1 | a0006c0015t0050g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.317-7637A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037125 | |||||||
chr3:125037150 | C | T | 3 | a0021c0023t0031g0183 a0021c0023t0031g0190 a0021c0023t0031g0191 |
3 | HG03098.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.317-7662G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037150 | |||||||
chr3:125037175 | T | C | 19 | a0003c0004t0020g0063 a0003c0004t0025g0271 a0003c0067t0019g0064 others(16): Show |
19 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.317-7687A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037175 | |||||||
chr3:125037455 | T | C | 3 | a0004c0089t0026g0306 a0007c0060t0139g0217 a0024c0032t0026g0241 |
3 | HG02723.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.317-7967A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037455 | |||||||
chr3:125037546 | A | T | 28 | a0002c0003t0007g0149 a0003c0004t0020g0063 a0003c0004t0025g0271 others(25): Show |
28 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.317-8058T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037546 | |||||||
chr3:125037745 | C | T | 5 | a0003c0004t0020g0063 a0006c0015t0050g0065 a0011c0018t0034g0321 others(2): Show |
5 | HG00741.hp1 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-8257G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037745 | |||||||
chr3:125037823 | G | C | 44 | a0002c0003t0002g0157 a0002c0003t0003g0004 a0002c0003t0003g0005 others(41): Show |
47 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.317-8335C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037823 | |||||||
chr3:125037867 | G | C | 6 | a0005c0086t0090g0085 a0006c0076t0091g0162 a0018c0037t0063g0254 others(3): Show |
6 | HG02055.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-8379C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037867 | |||||||
chr3:125037888 | T | C | 1 | a0001c0001t0097g0145 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.317-8400A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037888 | |||||||
chr3:125037927 | C | T | 171 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(168): Show |
174 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.317-8439G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037927 | |||||||
chr3:125037934 | C | T | 1 | a0001c0001t0059g0260 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.317-8446G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125037934 | |||||||
chr3:125038023 | T | C | 1 | a0002c0005t0043g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.317-8535A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038023 | |||||||
chr3:125038051 | A | G | 101 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(98): Show |
103 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.317-8563T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038051 | |||||||
chr3:125038409 | C | T | 1 | a0038c0079t0079g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.317-8921G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038409 | |||||||
chr3:125038474 | T | C | 292 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(289): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.317-8986A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038474 | |||||||
chr3:125038517 | G | A | 2 | a0001c0001t0044g0104 a0001c0001t0100g0096 |
2 | HG01243.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.317-9029C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038517 | |||||||
chr3:125038572 | C | A | 1 | a0001c0001t0059g0260 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.317-9084G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038572 | |||||||
chr3:125038757 | G | A | 1 | a0007c0013t0058g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.317-9269C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038757 | |||||||
chr3:125038858 | A | G | 3 | a0001c0002t0051g0137 a0001c0002t0051g0138 a0001c0010t0033g0020 |
3 | HG00099.hp2 HG01256.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.317-9370T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038858 | |||||||
chr3:125038919 | G | A | 3 | a0001c0001t0070g0195 a0002c0005t0010g0166 a0036c0069t0111g0202 |
3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.317-9431C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038919 | |||||||
chr3:125038920 | C | T | 3 | a0001c0001t0070g0195 a0002c0005t0010g0166 a0036c0069t0111g0202 |
3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.317-9432G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038920 | |||||||
chr3:125038933 | T | C | 55 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(52): Show |
56 | HG00558.hp1 HG00735.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-9445A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038933 | |||||||
chr3:125038948 | G | A | 1 | a0001c0001t0008g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.317-9460C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125038948 | |||||||
chr3:125039011 | C | A | 1 | a0016c0025t0025g0009 | 2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.317-9523G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039011 | |||||||
chr3:125039044 | T | C | 195 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.317-9556A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039044 | |||||||
chr3:125039108 | G | C | 1 | a0001c0001t0042g0098 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.317-9620C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039108 | |||||||
chr3:125039123 | T | C | 1 | a0001c0002t0001g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.317-9635A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039123 | |||||||
chr3:125039467 | C | T | 6 | a0001c0001t0059g0260 a0004c0007t0055g0320 a0020c0043t0063g0340 others(3): Show |
6 | HG02148.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-9979G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039467 | |||||||
chr3:125039475 | C | T | 3 | a0002c0014t0006g0256 a0002c0014t0075g0079 a0002c0014t0121g0255 |
3 | NA19012.hp2 NA19067.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.317-9987G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039475 | |||||||
chr3:125039835 | C | CA | 14 | a0002c0048t0029g0025 a0003c0004t0002g0090 a0004c0007t0055g0320 others(11): Show |
14 | HG00621.hp1 HG02155.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-10348dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | |||||||
chr3:125039835 | C | CAA | 174 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.317-10349_317-1034 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | |||||||
chr3:125039835 | C | CAAA | 12 | a0001c0001t0004g0277 a0001c0001t0006g0281 a0001c0001t0007g0114 others(9): Show |
12 | HG01167.hp1 HG01346.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.317-10350_317-1034 others(7): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | |||||||
chr3:125039835 | CA | C | 83 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(80): Show |
84 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.317-10348delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039835 | |||||||
chr3:125039842 | AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0016g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.317-10365_317-1035 others(15): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039842 | |||||||
chr3:125039853 | C | A | 47 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(44): Show |
48 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.317-10365G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039853 | |||||||
chr3:125039863 | C | G | 1 | a0001c0085t0132g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.317-10375G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125039863 | |||||||
chr3:125040103 | C | T | 2 | a0004c0007t0060g0332 a0004c0007t0137g0335 |
2 | HG02155.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.317-10615G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040103 | |||||||
chr3:125040107 | G | T | 4 | a0005c0086t0090g0085 a0016c0025t0025g0009 a0016c0025t0130g0316 others(1): Show |
5 | HG00735.hp2 HG01074.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-10619C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040107 | |||||||
chr3:125040213 | C | T | 336 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(333): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.317-10725G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040213 | |||||||
chr3:125040294 | T | C | 1 | a0002c0005t0028g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.317-10806A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040294 | |||||||
chr3:125040357 | T | A | 44 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(41): Show |
44 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.317-10869A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040357 | |||||||
chr3:125040476 | G | A | 1 | a0001c0002t0072g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.317-10988C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040476 | |||||||
chr3:125040503 | T | C | 48 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(45): Show |
49 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-11015A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040503 | |||||||
chr3:125040521 | G | A | 4 | a0005c0086t0090g0085 a0016c0025t0025g0009 a0016c0025t0130g0316 others(1): Show |
5 | HG00735.hp2 HG01074.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-11033C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040521 | |||||||
chr3:125040694 | G | C | 1 | a0006c0011t0011g0125 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.317-11206C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040694 | |||||||
chr3:125040711 | CT | C | 118 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(115): Show |
120 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.317-11224delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040711 | |||||||
chr3:125040711 | CTT | C | 24 | a0002c0005t0010g0201 a0002c0081t0116g0244 a0003c0004t0020g0063 others(21): Show |
24 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.317-11225_317-1122 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125040711 | |||||||
chr3:125041002 | C | T | 22 | a0002c0005t0010g0201 a0002c0081t0116g0244 a0003c0004t0020g0063 others(19): Show |
22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.317-11514G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041002 | |||||||
chr3:125041222 | T | A | 19 | a0001c0001t0059g0260 a0002c0005t0010g0045 a0004c0007t0055g0320 others(16): Show |
19 | HG01346.hp1 HG02148.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.317-11734A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041222 | |||||||
chr3:125041242 | G | A | 142 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(139): Show |
144 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.317-11754C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041242 | |||||||
chr3:125041270 | G | T | 42 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(39): Show |
42 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.317-11782C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041270 | |||||||
chr3:125041554 | A | C | 20 | a0001c0001t0059g0260 a0002c0005t0010g0045 a0004c0007t0055g0320 others(17): Show |
20 | HG01346.hp1 HG02148.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.317-12066T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041554 | |||||||
chr3:125041604 | G | C | 147 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(144): Show |
150 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.317-12116C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041604 | |||||||
chr3:125041644 | C | A | 1 | a0002c0005t0010g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317-12156G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041644 | |||||||
chr3:125041724 | A | C | 22 | a0002c0005t0010g0201 a0002c0081t0116g0244 a0003c0004t0020g0063 others(19): Show |
22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.317-12236T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041724 | |||||||
chr3:125041839 | G | T | 94 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(91): Show |
96 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.317-12351C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041839 | |||||||
chr3:125041908 | G | T | 40 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(37): Show |
40 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.317-12420C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125041908 | |||||||
chr3:125042047 | T | G | 5 | a0001c0001t0047g0123 a0001c0001t0047g0124 a0001c0001t0062g0278 others(2): Show |
5 | NA18942.hp1 NA18977.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-12559A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042047 | |||||||
chr3:125042376 | C | T | 22 | a0002c0005t0010g0201 a0002c0081t0116g0244 a0003c0004t0020g0063 others(19): Show |
22 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.317-12888G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042376 | |||||||
chr3:125042437 | T | TA | 29 | a0001c0002t0016g0062 a0001c0010t0001g0014 a0001c0010t0001g0026 others(26): Show |
29 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.317-12950dupT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042437 | |||||||
chr3:125042503 | G | A | 40 | a0001c0001t0011g0082 a0001c0001t0011g0184 a0001c0001t0092g0188 others(37): Show |
40 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.317-13015C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042503 | |||||||
chr3:125042582 | G | C | 9 | a0004c0007t0013g0305 a0004c0007t0013g0312 a0004c0007t0014g0308 others(6): Show |
9 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+12993C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042582 | |||||||
chr3:125042743 | T | C | 1 | a0001c0001t0011g0082 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.316+12832A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042743 | |||||||
chr3:125042751 | A | C | 239 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(236): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.316+12824T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042751 | |||||||
chr3:125042754 | A | C | 1 | a0002c0003t0089g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.316+12821T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042754 | |||||||
chr3:125042770 | A | G | 158 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(155): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.316+12805T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042770 | |||||||
chr3:125042882 | C | T | 3 | a0001c0001t0070g0195 a0002c0005t0010g0166 a0036c0069t0111g0202 |
3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.316+12693G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042882 | |||||||
chr3:125042883 | G | A | 1 | a0034c0061t0035g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.316+12692C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042883 | |||||||
chr3:125042918 | C | T | 1 | a0002c0003t0007g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.316+12657G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125042918 | |||||||
chr3:125043076 | T | C | 294 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.316+12499A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043076 | |||||||
chr3:125043077 | G | A | 1 | a0001c0002t0016g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.316+12498C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043077 | |||||||
chr3:125043123 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.316+12452C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043123 | |||||||
chr3:125043145 | C | T | 1 | a0002c0003t0078g0074 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.316+12430G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043145 | |||||||
chr3:125043391 | A | G | 1 | a0006c0077t0073g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.316+12184T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043391 | |||||||
chr3:125043420 | G | GT | 52 | a0001c0001t0093g0163 a0002c0003t0007g0070 a0002c0003t0007g0071 others(49): Show |
55 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.316+12154dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043420 | |||||||
chr3:125043420 | G | GTT | 16 | a0002c0003t0007g0077 a0002c0005t0010g0045 a0004c0007t0123g0349 others(13): Show |
16 | HG01346.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.316+12153_316+1215 others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043420 | |||||||
chr3:125043474 | T | C | 2 | a0003c0004t0039g0054 a0003c0034t0030g0115 |
2 | HG03239.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.316+12101A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043474 | |||||||
chr3:125043492 | A | T | 2 | a0002c0003t0082g0185 a0002c0071t0083g0186 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.316+12083T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043492 | |||||||
chr3:125043524 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.316+12051C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043524 | |||||||
chr3:125043957 | G | A | 2 | a0016c0025t0025g0009 a0016c0025t0130g0316 |
3 | HG00735.hp2 HG01074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.316+11618C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043957 | |||||||
chr3:125043963 | C | T | 1 | a0001c0001t0059g0260 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.316+11612G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125043963 | |||||||
chr3:125044080 | C | T | 39 | a0001c0001t0093g0163 a0002c0003t0007g0070 a0002c0003t0007g0071 others(36): Show |
42 | HG01975.hp2 HG02027.hp1 HG02074.hp2 others(39): Show |
intron_variant | MODIFIER | c.316+11495G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044080 | |||||||
chr3:125044087 | G | A | 1 | a0002c0003t0078g0074 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.316+11488C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044087 | |||||||
chr3:125044183 | G | C | 5 | a0001c0001t0011g0184 a0001c0001t0092g0188 a0004c0042t0134g0343 others(2): Show |
5 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+11392C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044183 | |||||||
chr3:125044297 | T | C | 1 | a0036c0069t0111g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+11278A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044297 | |||||||
chr3:125044385 | A | G | 111 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0007g0114 others(108): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.316+11190T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044385 | |||||||
chr3:125044472 | C | T | 38 | a0001c0001t0093g0163 a0002c0003t0007g0070 a0002c0003t0007g0071 others(35): Show |
41 | HG01975.hp2 HG02027.hp1 HG02074.hp2 others(38): Show |
intron_variant | MODIFIER | c.316+11103G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125044472 | |||||||
chr3:125045050 | G | A | 1 | a0001c0002t0145g0351 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.316+10525C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045050 | |||||||
chr3:125045084 | A | C | 104 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0007g0114 others(101): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.316+10491T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045084 | |||||||
chr3:125045266 | A | G | 98 | a0001c0001t0008g0242 a0001c0001t0029g0154 a0001c0001t0092g0188 others(95): Show |
101 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.316+10309T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045266 | |||||||
chr3:125045305 | C | T | 1 | a0001c0001t0008g0245 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.316+10270G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045305 | |||||||
chr3:125045306 | G | A | 1 | a0003c0067t0019g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.316+10269C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045306 | |||||||
chr3:125045377 | T | C | 1 | a0005c0086t0090g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+10198A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045377 | |||||||
chr3:125045463 | C | T | 97 | a0001c0001t0008g0242 a0001c0001t0029g0154 a0001c0001t0092g0188 others(94): Show |
100 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.316+10112G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045463 | |||||||
chr3:125045535 | G | A | 1 | a0026c0058t0057g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.316+10040C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045535 | |||||||
chr3:125045570 | G | A | 128 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0007g0114 others(125): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.316+10005C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045570 | |||||||
chr3:125045725 | C | T | 1 | a0015c0057t0128g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316+9850G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045725 | |||||||
chr3:125045740 | C | T | 1 | a0045c0073t0056g0297 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.316+9835G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045740 | |||||||
chr3:125045741 | G | A | 1 | a0041c0051t0023g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.316+9834C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045741 | |||||||
chr3:125045968 | C | T | 1 | a0005c0086t0090g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+9607G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125045968 | |||||||
chr3:125046132 | C | A | 1 | a0001c0001t0059g0260 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.316+9443G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046132 | |||||||
chr3:125046317 | C | T | 18 | a0001c0001t0008g0242 a0002c0005t0027g0258 a0002c0005t0028g0257 others(15): Show |
18 | HG00741.hp1 HG01256.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.316+9258G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046317 | |||||||
chr3:125046398 | T | TAC | 10 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0113g0151 others(7): Show |
10 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+9175_316+9176d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TAC | T | 25 | a0001c0001t0045g0129 a0001c0002t0001g0130 a0001c0002t0001g0131 others(22): Show |
27 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+9175_316+9176d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TACAC | T | 10 | a0001c0001t0008g0242 a0001c0001t0011g0082 a0001c0001t0070g0195 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+9173_316+9176d others(6): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TACACAC | T | 21 | a0001c0001t0059g0260 a0001c0001t0093g0163 a0002c0003t0003g0127 others(18): Show |
21 | HG00673.hp2 HG00741.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.316+9171_316+9176d others(8): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TACACACA others(1): Show |
T | 42 | a0001c0001t0023g0060 a0001c0001t0044g0104 a0001c0001t0100g0096 others(39): Show |
45 | HG00438.hp1 HG00544.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.316+9169_316+9176d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TACACACA others(3): Show |
T | 54 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(51): Show |
54 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.316+9167_316+9176d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TACACACA others(5): Show |
T | 26 | a0001c0001t0061g0288 a0001c0001t0126g0272 a0001c0001t0127g0299 others(23): Show |
27 | HG00733.hp1 HG01071.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+9165_316+9176d others(14): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046398 | TACACACA others(9): Show |
T | 1 | a0005c0086t0090g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+9161_316+9176d others(18): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046398 | |||||||
chr3:125046414 | C | G | 24 | a0001c0001t0061g0288 a0001c0001t0126g0272 a0001c0001t0127g0299 others(21): Show |
25 | HG00733.hp1 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.316+9161G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046414 | |||||||
chr3:125046428 | CACACACA others(1): Show |
C | 82 | a0001c0001t0029g0154 a0001c0001t0092g0188 a0001c0002t0016g0062 others(79): Show |
85 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.316+9139_316+9146d others(10): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046428 | |||||||
chr3:125046443 | T | A | 3 | a0001c0001t0008g0242 a0003c0004t0025g0271 a0006c0015t0115g0056 |
3 | HG02293.hp1 NA18959.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.316+9132A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046443 | |||||||
chr3:125046660 | T | C | 1 | a0002c0003t0003g0174 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.316+8915A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046660 | |||||||
chr3:125046763 | A | G | 26 | a0001c0001t0061g0288 a0001c0001t0126g0272 a0001c0001t0127g0299 others(23): Show |
27 | HG00733.hp1 HG01071.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+8812T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046763 | |||||||
chr3:125046979 | C | T | 3 | a0009c0016t0005g0221 a0025c0036t0030g0068 a0025c0036t0030g0120 |
3 | HG02083.hp2 HG02132.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.316+8596G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125046979 | |||||||
chr3:125047028 | G | A | 1 | a0002c0005t0010g0045 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.316+8547C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047028 | |||||||
chr3:125047402 | T | C | 3 | a0006c0011t0022g0003 a0006c0011t0086g0081 a0032c0064t0067g0010 |
4 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+8173A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047402 | |||||||
chr3:125047642 | T | C | 161 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.316+7933A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047642 | |||||||
chr3:125047735 | A | G | 1 | a0044c0084t0019g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+7840T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047735 | |||||||
chr3:125047882 | C | CT | 5 | a0002c0005t0009g0078 a0003c0004t0020g0063 a0003c0067t0019g0064 others(2): Show |
5 | HG01975.hp1 HG01981.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+7692dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125047882 | |||||||
chr3:125048015 | T | C | 101 | a0001c0001t0007g0114 a0001c0001t0012g0173 a0001c0001t0029g0154 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.316+7560A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048015 | |||||||
chr3:125048052 | G | C | 1 | a0040c0065t0066g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.316+7523C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048052 | |||||||
chr3:125048216 | A | C | 10 | a0001c0001t0012g0173 a0002c0003t0003g0174 a0003c0004t0002g0001 others(7): Show |
12 | HG02027.hp1 NA18951.hp2 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.316+7359T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048216 | |||||||
chr3:125048253 | T | C | 91 | a0001c0001t0007g0114 a0001c0001t0029g0154 a0001c0001t0042g0098 others(88): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.316+7322A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048253 | |||||||
chr3:125048306 | T | C | 23 | a0001c0001t0010g0069 a0001c0002t0001g0075 a0001c0002t0001g0080 others(20): Show |
23 | HG01346.hp1 HG02074.hp2 HG02132.hp2 others(20): Show |
intron_variant | MODIFIER | c.316+7269A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048306 | |||||||
chr3:125048389 | T | G | 35 | a0001c0001t0061g0288 a0001c0002t0005g0290 a0001c0002t0005g0296 others(32): Show |
36 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.316+7186A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048389 | |||||||
chr3:125048400 | T | C | 1 | a0009c0022t0004g0230 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.316+7175A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048400 | |||||||
chr3:125048607 | T | C | 2 | a0001c0001t0070g0195 a0002c0005t0010g0166 |
2 | HG01109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316+6968A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048607 | |||||||
chr3:125048691 | TGTTAAGC others(3): Show |
T | 1 | a0013c0017t0096g0049 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.316+6874_316+6883d others(12): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048691 | |||||||
chr3:125048801 | G | T | 1 | a0004c0040t0059g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.316+6774C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048801 | |||||||
chr3:125048830 | A | G | 1 | a0011c0018t0055g0318 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.316+6745T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048830 | |||||||
chr3:125048832 | G | A | 36 | a0001c0001t0061g0288 a0001c0002t0005g0290 a0001c0002t0005g0296 others(33): Show |
37 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.316+6743C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048832 | |||||||
chr3:125048856 | G | C | 2 | a0002c0005t0009g0078 a0002c0014t0075g0079 |
2 | NA18955.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.316+6719C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125048856 | |||||||
chr3:125049066 | A | G | 9 | a0001c0001t0011g0082 a0006c0011t0022g0003 a0006c0011t0086g0081 others(6): Show |
10 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+6509T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049066 | |||||||
chr3:125049092 | G | A | 1 | a0001c0010t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.316+6483C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049092 | |||||||
chr3:125049137 | T | A | 3 | a0002c0005t0010g0067 a0005c0006t0088g0066 a0005c0086t0090g0085 |
3 | HG02280.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316+6438A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049137 | |||||||
chr3:125049257 | ACTTACAT others(4): Show |
A | 1 | a0002c0003t0015g0084 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.316+6307_316+6317d others(13): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049257 | |||||||
chr3:125049264 | T | C | 3 | a0004c0007t0123g0349 a0011c0018t0056g0350 a0028c0090t0119g0348 |
3 | HG00639.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.316+6311A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049264 | |||||||
chr3:125049288 | T | C | 1 | a0008c0009t0138g0346 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.316+6287A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049288 | |||||||
chr3:125049376 | G | A | 8 | a0001c0002t0016g0062 a0002c0005t0010g0067 a0003c0004t0020g0063 others(5): Show |
8 | HG01981.hp1 HG02280.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+6199C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049376 | |||||||
chr3:125049522 | A | G | 96 | a0001c0001t0007g0114 a0001c0001t0029g0154 a0001c0001t0042g0098 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.316+6053T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049522 | |||||||
chr3:125049687 | T | G | 1 | a0004c0007t0013g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.316+5888A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049687 | |||||||
chr3:125049761 | C | T | 9 | a0001c0001t0011g0082 a0006c0011t0022g0003 a0006c0011t0086g0081 others(6): Show |
10 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+5814G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049761 | |||||||
chr3:125049803 | G | A | 1 | a0009c0022t0008g0231 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.316+5772C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049803 | |||||||
chr3:125049827 | G | A | 3 | a0004c0007t0123g0349 a0011c0018t0056g0350 a0028c0090t0119g0348 |
3 | HG00639.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.316+5748C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125049827 | |||||||
chr3:125050130 | T | G | 1 | a0002c0005t0042g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.316+5445A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050130 | |||||||
chr3:125050142 | C | CT | 11 | a0001c0002t0016g0062 a0004c0007t0013g0305 a0004c0007t0013g0312 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+5432dupA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050142 | |||||||
chr3:125050142 | CT | C | 160 | a0001c0001t0004g0293 a0001c0001t0004g0294 a0001c0001t0007g0114 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.316+5432delA | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050142 | |||||||
chr3:125050142 | CTT | C | 28 | a0001c0002t0001g0080 a0001c0002t0016g0052 a0001c0002t0033g0051 others(25): Show |
28 | HG00621.hp1 HG00639.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.316+5431_316+5432d others(4): Show |
HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050142 | |||||||
chr3:125050144 | T | C | 2 | a0002c0005t0010g0201 a0036c0069t0111g0202 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316+5431A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050144 | |||||||
chr3:125050145 | T | C | 4 | a0003c0004t0002g0090 a0005c0006t0022g0089 a0006c0077t0073g0088 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+5430A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050145 | |||||||
chr3:125050166 | T | A | 8 | a0001c0002t0016g0062 a0002c0005t0010g0067 a0003c0004t0020g0063 others(5): Show |
8 | HG01981.hp1 HG02280.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+5409A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050166 | |||||||
chr3:125050213 | G | A | 20 | a0001c0010t0001g0014 a0001c0010t0001g0023 a0001c0010t0001g0026 others(17): Show |
20 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+5362C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050213 | |||||||
chr3:125050278 | G | A | 1 | a0037c0050t0022g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+5297C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050278 | |||||||
chr3:125050391 | G | A | 9 | a0001c0001t0011g0082 a0006c0011t0022g0003 a0006c0011t0086g0081 others(6): Show |
10 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.316+5184C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050391 | |||||||
chr3:125050424 | G | A | 1 | a0019c0026t0117g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.316+5151C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050424 | |||||||
chr3:125050442 | C | A | 1 | a0001c0001t0044g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.316+5133G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050442 | |||||||
chr3:125050554 | C | G | 4 | a0004c0007t0123g0349 a0004c0042t0004g0347 a0011c0018t0056g0350 others(1): Show |
4 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+5021G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050554 | |||||||
chr3:125050573 | A | G | 1 | a0002c0081t0116g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.316+5002T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050573 | |||||||
chr3:125050581 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.316+4994G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050581 | |||||||
chr3:125050840 | A | G | 24 | a0001c0002t0016g0052 a0001c0002t0033g0051 a0001c0010t0001g0014 others(21): Show |
24 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(21): Show |
intron_variant | MODIFIER | c.316+4735T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050840 | |||||||
chr3:125050868 | T | C | 33 | a0001c0001t0011g0082 a0001c0002t0016g0052 a0001c0002t0033g0051 others(30): Show |
34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+4707A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050868 | |||||||
chr3:125050942 | T | C | 5 | a0024c0032t0065g0012 a0032c0064t0067g0010 a0035c0066t0068g0011 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+4633A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050942 | |||||||
chr3:125050952 | C | T | 7 | a0010c0008t0004g0236 a0010c0008t0027g0234 a0010c0008t0027g0235 others(4): Show |
7 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+4623G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125050952 | |||||||
chr3:125051016 | T | C | 2 | a0001c0002t0005g0296 a0005c0006t0118g0295 |
2 | HG00733.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.316+4559A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051016 | |||||||
chr3:125051221 | T | A | 1 | a0005c0086t0090g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+4354A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051221 | |||||||
chr3:125051238 | A | G | 10 | a0012c0030t0048g0037 a0012c0030t0048g0038 a0014c0053t0001g0034 others(7): Show |
10 | HG00323.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+4337T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051238 | |||||||
chr3:125051346 | CG | C | 33 | a0001c0001t0011g0082 a0001c0002t0016g0052 a0001c0002t0033g0051 others(30): Show |
34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+4228delC | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051346 | |||||||
chr3:125051347 | G | A | 6 | a0002c0005t0010g0201 a0003c0004t0002g0090 a0005c0006t0022g0089 others(3): Show |
6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+4228C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051347 | |||||||
chr3:125051391 | A | AC | 6 | a0001c0001t0100g0096 a0001c0002t0001g0092 a0001c0002t0038g0243 others(3): Show |
6 | HG00741.hp2 HG01243.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+4183dupG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051391 | |||||||
chr3:125051456 | C | G | 33 | a0001c0001t0011g0082 a0001c0002t0016g0052 a0001c0002t0033g0051 others(30): Show |
34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+4119G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051456 | |||||||
chr3:125051486 | T | A | 1 | a0023c0031t0012g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.316+4089A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051486 | |||||||
chr3:125051493 | G | C | 5 | a0024c0032t0065g0012 a0032c0064t0067g0010 a0035c0066t0068g0011 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+4082C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051493 | |||||||
chr3:125051515 | C | T | 1 | a0002c0005t0010g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.316+4060G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051515 | |||||||
chr3:125051569 | A | G | 191 | a0001c0001t0007g0114 a0001c0001t0010g0069 a0001c0001t0011g0082 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.316+4006T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051569 | |||||||
chr3:125051574 | A | G | 1 | a0006c0015t0115g0056 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.316+4001T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051574 | |||||||
chr3:125051598 | G | A | 1 | a0003c0068t0084g0197 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.316+3977C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051598 | |||||||
chr3:125051609 | C | T | 3 | a0019c0026t0053g0302 a0019c0026t0053g0303 a0019c0026t0117g0304 |
3 | HG02109.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.316+3966G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051609 | |||||||
chr3:125051641 | C | T | 1 | a0007c0013t0004g0211 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.316+3934G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051641 | |||||||
chr3:125051693 | T | C | 193 | a0001c0001t0007g0114 a0001c0001t0010g0069 a0001c0001t0011g0082 others(190): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.316+3882A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051693 | |||||||
chr3:125051833 | G | C | 24 | a0001c0002t0016g0052 a0001c0002t0033g0051 a0001c0010t0001g0014 others(21): Show |
24 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(21): Show |
intron_variant | MODIFIER | c.316+3742C>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125051833 | |||||||
chr3:125052109 | AC | A | 9 | a0012c0030t0048g0037 a0012c0030t0048g0038 a0014c0053t0001g0034 others(6): Show |
9 | HG01361.hp1 HG01433.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+3465delG | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052109 | |||||||
chr3:125052126 | G | A | 146 | a0001c0001t0007g0114 a0001c0001t0010g0069 a0001c0001t0011g0184 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.316+3449C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052126 | |||||||
chr3:125052131 | C | T | 1 | a0001c0010t0001g0014 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316+3444G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052131 | |||||||
chr3:125052132 | T | G | 33 | a0001c0001t0011g0082 a0001c0002t0016g0052 a0001c0002t0033g0051 others(30): Show |
34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+3443A>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052132 | |||||||
chr3:125052139 | T | C | 1 | a0013c0017t0096g0049 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.316+3436A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052139 | |||||||
chr3:125052237 | C | A | 1 | a0002c0005t0011g0198 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.316+3338G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052237 | |||||||
chr3:125052241 | C | T | 19 | a0004c0007t0013g0305 a0004c0007t0013g0312 a0004c0007t0014g0308 others(16): Show |
19 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.316+3334G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052241 | |||||||
chr3:125052265 | C | T | 1 | a0001c0001t0008g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.316+3310G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052265 | |||||||
chr3:125052293 | G | A | 2 | a0002c0005t0010g0201 a0036c0069t0111g0202 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316+3282C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052293 | |||||||
chr3:125052388 | C | A | 218 | a0001c0001t0007g0114 a0001c0001t0010g0069 a0001c0001t0011g0082 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.316+3187G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052388 | |||||||
chr3:125052407 | C | T | 4 | a0024c0032t0065g0012 a0032c0064t0067g0010 a0035c0066t0068g0011 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+3168G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052407 | |||||||
chr3:125052454 | G | A | 1 | a0001c0002t0005g0298 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.316+3121C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052454 | |||||||
chr3:125052861 | C | T | 85 | a0001c0001t0007g0114 a0001c0001t0029g0154 a0001c0001t0042g0098 others(82): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.316+2714G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052861 | |||||||
chr3:125052936 | G | T | 1 | a0004c0038t0131g0301 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.316+2639C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125052936 | |||||||
chr3:125053033 | A | C | 33 | a0001c0001t0011g0082 a0001c0002t0016g0052 a0001c0002t0033g0051 others(30): Show |
34 | HG00621.hp1 HG00639.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.316+2542T>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053033 | |||||||
chr3:125053060 | C | T | 4 | a0001c0002t0001g0092 a0001c0002t0024g0093 a0001c0002t0024g0094 others(1): Show |
4 | HG00140.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+2515G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053060 | |||||||
chr3:125053238 | C | T | 146 | a0001c0001t0007g0114 a0001c0001t0010g0069 a0001c0001t0011g0184 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.316+2337G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053238 | |||||||
chr3:125053300 | A | G | 1 | a0044c0084t0019g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.316+2275T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053300 | |||||||
chr3:125053520 | T | C | 3 | a0010c0008t0036g0238 a0010c0008t0036g0239 a0010c0008t0036g0240 |
3 | HG00738.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.316+2055A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053520 | |||||||
chr3:125053679 | A | G | 25 | a0007c0012t0013g0225 a0007c0012t0013g0226 a0007c0012t0017g0002 others(22): Show |
27 | HG00558.hp1 HG00558.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.316+1896T>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053679 | |||||||
chr3:125053724 | T | C | 1 | a0014c0055t0002g0041 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.316+1851A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053724 | |||||||
chr3:125053747 | C | T | 9 | a0005c0086t0090g0085 a0012c0030t0048g0037 a0012c0030t0048g0038 others(6): Show |
9 | HG01361.hp1 HG01433.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.316+1828G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053747 | |||||||
chr3:125053871 | C | T | 19 | a0001c0001t0010g0069 a0001c0001t0011g0082 a0001c0002t0001g0075 others(16): Show |
20 | HG01884.hp2 HG02074.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+1704G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053871 | |||||||
chr3:125053927 | C | G | 1 | a0013c0087t0021g0091 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.316+1648G>C | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125053927 | |||||||
chr3:125054069 | G | A | 54 | a0001c0001t0010g0069 a0001c0001t0011g0082 a0001c0002t0001g0075 others(51): Show |
55 | HG00621.hp1 HG00639.hp2 HG01361.hp1 others(52): Show |
intron_variant | MODIFIER | c.316+1506C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054069 | |||||||
chr3:125054139 | T | C | 5 | a0003c0004t0002g0090 a0005c0006t0022g0089 a0006c0077t0073g0088 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+1436A>G | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054139 | |||||||
chr3:125054326 | CA | C | 20 | a0001c0010t0001g0014 a0001c0010t0001g0023 a0001c0010t0001g0026 others(17): Show |
20 | HG00621.hp1 HG00639.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+1248delT | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054326 | |||||||
chr3:125054669 | C | T | 1 | a0002c0003t0003g0004 | 2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.316+906G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054669 | |||||||
chr3:125054831 | G | A | 125 | a0001c0001t0007g0114 a0001c0001t0011g0184 a0001c0001t0012g0173 others(122): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.316+744C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054831 | |||||||
chr3:125054910 | G | A | 1 | a0024c0032t0026g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.316+665C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125054910 | |||||||
chr3:125055052 | C | A | 1 | a0007c0013t0124g0232 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.316+523G>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055052 | |||||||
chr3:125055415 | T | A | 4 | a0004c0007t0123g0349 a0004c0042t0004g0347 a0011c0018t0056g0350 others(1): Show |
4 | HG00639.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+160A>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055415 | |||||||
chr3:125055446 | A | T | 1 | a0001c0001t0077g0044 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.316+129T>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055446 | |||||||
chr3:125055476 | G | T | 1 | a0005c0006t0009g0043 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.316+99C>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055476 | |||||||
chr3:125055516 | G | A | 2 | a0002c0005t0010g0201 a0036c0069t0111g0202 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316+59C>T | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055516 | |||||||
chr3:125055564 | C | T | 1 | a0015c0057t0128g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316+11G>A | HEG1 | ENSG00000173706.15 | transcript | ENST00000311127.9 | protein_coding | 1/16 | chr3 | 125055564 |