Item | Value |
---|---|
geneid | 80854 |
ensemblid | ENSG00000145391.14 |
hgncid | 30412 |
symbol | SETD7 |
name | SET domain containing 7, histone lysine methyltransferase |
refseq_nuc | NM_030648.4 |
refseq_prot | NP_085151.1 |
ensembl_nuc | ENST00000274031.8 |
ensembl_prot | ENSP00000274031.3 |
mane_status | MANE Select |
chr | chr4 |
start | 139506038 |
end | 139556219 |
strand | - |
ver | v1.2 |
region | chr4:139506038-139556219 |
region5000 | chr4:139501038-139561219 |
regionname0 | SETD7_chr4_139506038_139556219 |
regionname5000 | SETD7_chr4_139501038_139561219 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 366 | 313 | 95 | 60 | 104 | 17 | 36 | 66 | SETD7_chr4_139501038_139561219 | SETD7 | MDSDD others(361): Show |
chr4 | 139501038 | 139561219 |
a0002 | 0/1 | 366 | 3 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | MDSDD others(361): Show |
chr4 | 139501038 | 139561219 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1098 | 298 | 89 | 57 | 99 | 17 | 35 | SETD7_chr4_139501038_139561219 | SETD7 | ATGGA others(1093): Show |
chr4 | 139501038 | 139561219 | ||
a0001c0002 | 0/0 | 1098 | 8 | 1 | 3 | 4 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | ATGGA others(1093): Show |
chr4 | 139501038 | 139561219 | ||
a0001c0004 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | ATGGA others(1093): Show |
chr4 | 139501038 | 139561219 | ||
a0001c0005 | 0/0 | 1098 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | ATGGA others(1093): Show |
chr4 | 139501038 | 139561219 | ||
a0001c0006 | 0/0 | 1098 | 2 | 0 | 0 | 1 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | ATGGA others(1093): Show |
chr4 | 139501038 | 139561219 | ||
a0002c0003 | 0/1 | 1098 | 3 | 1 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | ATGGA others(1093): Show |
chr4 | 139501038 | 139561219 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6792 | 190 | 30 | 44 | 85 | 10 | 21 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0002 | 0/0 | 6808 | 16 | 1 | 6 | 0 | 1 | 8 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0003 | 0/0 | 6792 | 9 | 9 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0004 | 0/0 | 6808 | 7 | 7 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0005 | 0/0 | 6808 | 6 | 5 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0006 | 0/0 | 6808 | 3 | 0 | 0 | 0 | 2 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0007 | 0/0 | 6808 | 4 | 4 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0008 | 0/0 | 6792 | 3 | 0 | 0 | 3 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0009 | 0/0 | 6792 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0011 | 0/0 | 6808 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0012 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0013 | 0/0 | 6808 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0014 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0015 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0016 | 0/0 | 6792 | 2 | 0 | 0 | 0 | 2 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0017 | 0/0 | 6792 | 2 | 1 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0018 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0019 | 0/0 | 6792 | 2 | 0 | 0 | 0 | 1 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0020 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0021 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0022 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0023 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0024 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0025 | 1/0 | 6808 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0026 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0027 | 0/0 | 6808 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0028 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0029 | 0/0 | 6808 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0030 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0031 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0032 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0034 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0035 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0036 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0037 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0038 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0039 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0040 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0041 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0042 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0043 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0044 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0046 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0047 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0048 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0049 | 0/0 | 6808 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0050 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0051 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0052 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0053 | 0/0 | 6808 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0055 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0056 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0057 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0059 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0001t0060 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0002t0001 | 0/0 | 6792 | 3 | 0 | 0 | 3 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0002t0006 | 0/0 | 6808 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0002t0010 | 0/0 | 6808 | 3 | 1 | 1 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0004t0001 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0004t0012 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0004t0033 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0005t0054 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0005t0058 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6803): Show |
chr4 | 139501038 | 139561219 |
a0001c0006t0018 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0001c0006t0045 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
a0002c0003t0001 | 0/1 | 6792 | 3 | 1 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | AGAGC others(6787): Show |
chr4 | 139501038 | 139561219 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0006g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0012g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0012g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0013g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0015g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0016g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0016g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0017g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0018g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0019g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0021g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0022g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0023g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0024g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0025g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0026g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0027g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0028g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0029g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0030g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0031g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0032g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0034g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0035g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0036g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0037g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0038g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0039g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0040g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0041g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0042g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0043g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0044g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0046g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0047g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0048g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0049g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0050g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0051g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0052g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0053g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0055g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0056g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0057g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0059g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0060g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0010g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0004t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0004t0033g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0005t0054g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0005t0058g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0006t0018g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0006t0045g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0002c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0002c0003t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0048 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00323 | hp2 | a0001 | c0001 | t0019 | g0105 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00423 | hp2 | a0001 | c0001 | t0018 | g0082 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00438 | hp1 | a0001 | c0006 | t0045 | g0265 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00642 | hp2 | a0001 | c0002 | t0006 | g0134 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00741 | hp2 | a0001 | c0001 | t0044 | g0049 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01074 | hp1 | a0001 | c0001 | t0048 | g0085 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01074 | hp2 | a0001 | c0002 | t0006 | g0135 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01106 | hp2 | a0001 | c0001 | t0017 | g0034 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01192 | hp1 | a0001 | c0001 | t0053 | g0283 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0061 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01496 | hp1 | a0001 | c0001 | t0049 | g0235 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0006 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01516 | hp2 | a0001 | c0001 | t0016 | g0261 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0006 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01517 | hp2 | a0001 | c0001 | t0016 | g0263 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01884 | hp2 | a0001 | c0001 | t0026 | g0035 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01978 | hp1 | a0001 | c0001 | t0050 | g0205 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02040 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02055 | hp2 | a0001 | c0001 | t0031 | g0226 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0056 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02148 | hp2 | a0001 | c0002 | t0010 | g0264 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02257 | hp1 | a0001 | c0001 | t0040 | g0287 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0120 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0229 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0238 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02572 | hp2 | a0001 | c0001 | t0038 | g0221 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02717 | hp1 | a0001 | c0004 | t0012 | g0250 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0007 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0241 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02818 | hp1 | a0001 | c0001 | t0057 | g0228 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02886 | hp1 | a0001 | c0001 | t0032 | g0084 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0007 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02965 | hp1 | a0001 | c0001 | t0024 | g0133 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02965 | hp2 | a0001 | c0005 | t0058 | g0281 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0144 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03017 | hp1 | a0001 | c0001 | t0034 | g0225 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03017 | hp2 | a0001 | c0001 | t0019 | g0051 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03041 | hp2 | a0001 | c0005 | t0054 | g0282 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03098 | hp1 | a0001 | c0002 | t0010 | g0175 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0251 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03195 | hp1 | a0001 | c0001 | t0052 | g0043 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0145 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0124 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0179 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03225 | hp2 | a0001 | c0001 | t0055 | g0231 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03453 | hp2 | a0001 | c0001 | t0030 | g0244 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03486 | hp1 | a0001 | c0001 | t0014 | g0055 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03486 | hp2 | a0001 | c0001 | t0035 | g0023 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03491 | hp1 | a0001 | c0006 | t0018 | g0066 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03516 | hp1 | a0001 | c0004 | t0033 | g0070 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0237 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0187 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03710 | hp2 | a0001 | c0001 | t0043 | g0255 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03834 | hp1 | a0001 | c0001 | t0029 | g0189 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0031 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04199 | hp2 | a0001 | c0001 | t0041 | g0213 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18906 | hp1 | a0001 | c0001 | t0051 | g0143 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18947 | hp1 | a0001 | c0001 | t0023 | g0234 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0268 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18971 | hp2 | a0001 | c0002 | t0010 | g0207 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18974 | hp1 | a0001 | c0001 | t0036 | g0108 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18977 | hp1 | a0001 | c0001 | t0021 | g0079 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18983 | hp2 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18986 | hp1 | a0001 | c0001 | t0022 | g0269 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18986 | hp2 | a0001 | c0001 | t0060 | g0290 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18997 | hp1 | a0001 | c0001 | t0037 | g0104 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18997 | hp2 | a0001 | c0001 | t0047 | g0191 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19009 | hp2 | a0001 | c0001 | t0027 | g0050 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19012 | hp2 | a0001 | c0001 | t0059 | g0110 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19030 | hp2 | a0001 | c0001 | t0056 | g0032 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19056 | hp1 | a0001 | c0001 | t0042 | g0098 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0211 | AFR | ASW | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20805 | hp2 | a0001 | c0001 | t0039 | g0256 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02486 | hp1 | a0001 | c0001 | t0028 | g0214 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02559 | hp2 | a0001 | c0001 | t0046 | g0288 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0021 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20300 | hp2 | a0001 | c0001 | t0012 | g0227 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0123 | REF | REF | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
homoSapiens | grch38p0 | a0001 | c0001 | t0025 | g0107 | REF | REF | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139523358 | C | T | 1 | a0002 | 2 | HG00099.hp2 HG02257.hp2 |
missense_variant | MODERATE | c.640G>A | p.Glu214Lys | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/8 | 722/6808 | 640/1101 | 214/366 | chr4 | 139523358 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139529050 | G | A | 1 | a0001c0006 | 2 | HG00438.hp1 HG03491.hp1 |
synonymous_variant | LOW | c.543C>T | p.His181His | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/8 | 625/6808 | 543/1101 | 181/366 | chr4 | 139529050 | |||
chr4:139529155 | A | G | 1 | a0001c0002 | 8 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(5): Show |
synonymous_variant | LOW | c.438T>C | p.Tyr146Tyr | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/8 | 520/6808 | 438/1101 | 146/366 | chr4 | 139529155 | |||
chr4:139533261 | G | A | 1 | a0001c0004 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.276C>T | p.Asn92Asn | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/8 | 358/6808 | 276/1101 | 92/366 | chr4 | 139533261 | |||
chr4:139547024 | C | T | 1 | a0001c0005 | 2 | HG02965.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.66G>A | p.Pro22Pro | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/8 | 148/6808 | 66/1101 | 22/366 | chr4 | 139547024 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139506341 | G | A | 2 | a0001c0001t0003 a0001c0001t0005 |
15 | HG01361.hp1 HG01884.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5322C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5322 | chr4 | 139506341 | ||||||
chr4:139506483 | G | A | 1 | a0001c0001t0052 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5180C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5180 | chr4 | 139506483 | ||||||
chr4:139506495 | C | G | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5168G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5168 | chr4 | 139506495 | ||||||
chr4:139506603 | A | G | 1 | a0001c0001t0040 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5060T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5060 | chr4 | 139506603 | ||||||
chr4:139506707 | C | A | 1 | a0001c0005t0054 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4956G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4956 | chr4 | 139506707 | ||||||
chr4:139506810 | G | C | 1 | a0001c0001t0052 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4853C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4853 | chr4 | 139506810 | ||||||
chr4:139506827 | A | G | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4836T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4836 | chr4 | 139506827 | ||||||
chr4:139506884 | G | A | 1 | a0001c0001t0041 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4779C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4779 | chr4 | 139506884 | ||||||
chr4:139506890 | C | T | 1 | a0001c0001t0039 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4773G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4773 | chr4 | 139506890 | ||||||
chr4:139507011 | C | T | 1 | a0001c0001t0019 | 2 | HG00323.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4652G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4652 | chr4 | 139507011 | ||||||
chr4:139507014 | G | A | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4649C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4649 | chr4 | 139507014 | ||||||
chr4:139507108 | G | A | 1 | a0001c0001t0042 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4555C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4555 | chr4 | 139507108 | ||||||
chr4:139507145 | C | T | 2 | a0001c0001t0008 a0001c0001t0022 |
4 | HG02040.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4518G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4518 | chr4 | 139507145 | ||||||
chr4:139507209 | A | T | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4454T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4454 | chr4 | 139507209 | ||||||
chr4:139507377 | G | A | 2 | a0001c0001t0052 a0001c0001t0055 |
2 | HG03195.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4286C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4286 | chr4 | 139507377 | ||||||
chr4:139507676 | C | T | 1 | a0001c0001t0038 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3987G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3987 | chr4 | 139507676 | ||||||
chr4:139508162 | T | C | 1 | a0001c0001t0043 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3501A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3501 | chr4 | 139508162 | ||||||
chr4:139508258 | T | G | 2 | a0001c0001t0004 a0001c0001t0028 |
8 | HG02055.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3405A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3405 | chr4 | 139508258 | ||||||
chr4:139508364 | C | T | 2 | a0001c0001t0018 a0001c0006t0018 |
2 | HG00423.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3299G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3299 | chr4 | 139508364 | ||||||
chr4:139508401 | C | T | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
77 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3262G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3262 | chr4 | 139508401 | ||||||
chr4:139508410 | C | T | 2 | a0001c0001t0007 a0001c0001t0015 |
6 | HG02809.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3253G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3253 | chr4 | 139508410 | ||||||
chr4:139508445 | T | C | 1 | a0001c0001t0013 | 3 | HG02145.hp2 HG02809.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3218A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3218 | chr4 | 139508445 | ||||||
chr4:139508446 | G | A | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3217C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3217 | chr4 | 139508446 | ||||||
chr4:139508615 | C | T | 1 | a0001c0001t0037 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3048 | chr4 | 139508615 | ||||||
chr4:139508625 | C | T | 1 | a0001c0001t0047 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3038G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3038 | chr4 | 139508625 | ||||||
chr4:139508648 | G | A | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3015C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3015 | chr4 | 139508648 | ||||||
chr4:139508696 | G | A | 1 | a0001c0001t0044 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2967C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2967 | chr4 | 139508696 | ||||||
chr4:139508716 | G | A | 2 | a0001c0002t0010 a0001c0006t0045 |
4 | HG00438.hp1 HG02148.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2947C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2947 | chr4 | 139508716 | ||||||
chr4:139508775 | T | G | 1 | a0001c0001t0007 | 4 | HG02895.hp2 HG03130.hp1 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2888A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2888 | chr4 | 139508775 | ||||||
chr4:139508870 | C | G | 2 | a0001c0001t0049 a0001c0002t0010 |
4 | HG01496.hp1 HG02148.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2793G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2793 | chr4 | 139508870 | ||||||
chr4:139508907 | C | T | 1 | a0001c0001t0036 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2756G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2756 | chr4 | 139508907 | ||||||
chr4:139509054 | C | G | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
79 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2609G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2609 | chr4 | 139509054 | ||||||
chr4:139509074 | C | T | 1 | a0001c0001t0015 | 2 | HG02809.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2589G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2589 | chr4 | 139509074 | ||||||
chr4:139509102 | G | A | 8 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0026 others(5): Show |
11 | HG01192.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2561C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2561 | chr4 | 139509102 | ||||||
chr4:139509131 | G | A | 1 | a0001c0001t0009 | 3 | HG02280.hp1 HG03195.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2532C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2532 | chr4 | 139509131 | ||||||
chr4:139509150 | G | C | 1 | a0001c0001t0047 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2513C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2513 | chr4 | 139509150 | ||||||
chr4:139509157 | A | G | 6 | a0001c0001t0006 a0001c0001t0034 a0001c0001t0049 others(3): Show |
11 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2506T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2506 | chr4 | 139509157 | ||||||
chr4:139509278 | C | T | 1 | a0001c0004t0033 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2385 | chr4 | 139509278 | ||||||
chr4:139509344 | A | G | 1 | a0001c0001t0016 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2319T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2319 | chr4 | 139509344 | ||||||
chr4:139509422 | C | T | 1 | a0001c0005t0054 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2241G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2241 | chr4 | 139509422 | ||||||
chr4:139509427 | G | T | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2236 | chr4 | 139509427 | ||||||
chr4:139509471 | A | C | 38 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(35): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*2192T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2192 | chr4 | 139509471 | ||||||
chr4:139509471 | A | G | 1 | a0001c0001t0032 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2192T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2192 | chr4 | 139509471 | ||||||
chr4:139509537 | C | T | 1 | a0001c0001t0031 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2126G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2126 | chr4 | 139509537 | ||||||
chr4:139509592 | T | C | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*2071A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2071 | chr4 | 139509592 | ||||||
chr4:139510185 | C | T | 3 | a0001c0001t0020 a0001c0001t0051 a0001c0005t0058 |
4 | HG02965.hp2 HG03516.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1478G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1478 | chr4 | 139510185 | ||||||
chr4:139510238 | ACAGATCA others(9): Show |
A | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(34): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1409_*1424delCTGT others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1409 | chr4 | 139510238 | ||||||
chr4:139510350 | G | A | 1 | a0001c0001t0048 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1313 | chr4 | 139510350 | ||||||
chr4:139510356 | A | T | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1307 | chr4 | 139510356 | ||||||
chr4:139510635 | T | A | 2 | a0001c0001t0049 a0001c0005t0058 |
2 | HG01496.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1028A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1028 | chr4 | 139510635 | ||||||
chr4:139510757 | T | G | 1 | a0001c0001t0050 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*906A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 906 | chr4 | 139510757 | ||||||
chr4:139510777 | T | C | 16 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0012 others(13): Show |
27 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*886A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 886 | chr4 | 139510777 | ||||||
chr4:139510798 | C | T | 1 | a0001c0001t0023 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 865 | chr4 | 139510798 | ||||||
chr4:139511440 | A | T | 1 | a0001c0001t0022 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 223 | chr4 | 139511440 | ||||||
chr4:139511451 | C | T | 1 | a0001c0001t0021 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*212G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 212 | chr4 | 139511451 | ||||||
chr4:139511563 | G | A | 1 | a0001c0001t0059 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 100 | chr4 | 139511563 | ||||||
chr4:139556145 | G | A | 1 | a0001c0001t0060 | 1 | NA18986.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/8 | 8 | chr4 | 139556145 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139512042 | C | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0102 others(6): Show |
12 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.921-199G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512042 | |||||||
chr4:139512303 | G | T | 2 | a0001c0001t0001g0203 a0001c0001t0040g0287 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.921-460C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512303 | |||||||
chr4:139512311 | A | G | 4 | a0001c0001t0001g0182 a0001c0001t0009g0124 a0001c0001t0009g0145 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-468T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512311 | |||||||
chr4:139512434 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.921-591A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512434 | |||||||
chr4:139512483 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.921-640C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512483 | |||||||
chr4:139512595 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0009g0124 a0001c0001t0009g0145 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-752C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512595 | |||||||
chr4:139512670 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0060g0290 |
2 | NA18948.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.921-827T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512670 | |||||||
chr4:139512752 | C | CT | 12 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0045 others(9): Show |
14 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.921-910dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | |||||||
chr4:139512752 | CT | C | 15 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0011g0144 others(12): Show |
17 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.921-910delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | |||||||
chr4:139512752 | CTT | C | 27 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0039 others(24): Show |
29 | HG01361.hp1 HG02027.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-911_921-910del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | |||||||
chr4:139512752 | CTTT | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.921-912_921-910del others(3): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | |||||||
chr4:139512906 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.921-1063A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512906 | |||||||
chr4:139512945 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0197 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.921-1102C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512945 | |||||||
chr4:139513211 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.921-1368C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513211 | |||||||
chr4:139513272 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.921-1429A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513272 | |||||||
chr4:139513335 | G | A | 1 | a0001c0001t0029g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.921-1492C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513335 | |||||||
chr4:139513419 | C | CA | 18 | a0001c0001t0001g0041 a0001c0001t0001g0137 a0001c0001t0002g0005 others(15): Show |
20 | HG00099.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.921-1577dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513419 | |||||||
chr4:139513453 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.921-1610A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513453 | |||||||
chr4:139513586 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.921-1743A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513586 | |||||||
chr4:139513593 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0218 |
3 | HG01099.hp2 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.921-1750G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513593 | |||||||
chr4:139513730 | C | T | 1 | a0001c0001t0051g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.921-1887G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513730 | |||||||
chr4:139513878 | T | G | 1 | a0001c0001t0036g0108 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.921-2035A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513878 | |||||||
chr4:139513890 | A | G | 8 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0049g0235 others(5): Show |
9 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.921-2047T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513890 | |||||||
chr4:139513922 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-2079G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513922 | |||||||
chr4:139513977 | T | C | 1 | a0001c0005t0058g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.921-2134A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513977 | |||||||
chr4:139514052 | G | A | 1 | a0001c0001t0029g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.921-2209C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514052 | |||||||
chr4:139514135 | T | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.921-2292A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514135 | |||||||
chr4:139514163 | T | C | 55 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0045 others(52): Show |
60 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.921-2320A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514163 | |||||||
chr4:139514282 | GA | G | 78 | a0001c0001t0001g0037 a0001c0001t0001g0058 a0001c0001t0001g0071 others(75): Show |
85 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.921-2440delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514282 | |||||||
chr4:139514373 | C | A | 1 | a0001c0001t0015g0211 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.921-2530G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514373 | |||||||
chr4:139514385 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.921-2542G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514385 | |||||||
chr4:139514403 | G | T | 18 | a0001c0001t0011g0144 a0001c0001t0011g0187 a0001c0001t0011g0188 others(15): Show |
19 | HG01192.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.921-2560C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514403 | |||||||
chr4:139514468 | CAG | C | 65 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0045 others(62): Show |
72 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.921-2627_921-2626d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514468 | |||||||
chr4:139514478 | A | G | 1 | a0001c0001t0029g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.921-2635T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514478 | |||||||
chr4:139514482 | G | A | 1 | a0001c0001t0049g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.921-2639C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514482 | |||||||
chr4:139514581 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.921-2738G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514581 | |||||||
chr4:139514719 | C | T | 1 | a0001c0001t0030g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.921-2876G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514719 | |||||||
chr4:139515167 | CAA | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0118 a0001c0001t0001g0130 others(27): Show |
33 | HG01074.hp1 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.920+2716_920+2717d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | |||||||
chr4:139515167 | CAAA | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0024 others(79): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.920+2715_920+2717d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | |||||||
chr4:139515167 | CAAAA | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(164): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.920+2714_920+2717d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | |||||||
chr4:139515167 | CAAAAA | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0072 a0001c0001t0001g0218 others(4): Show |
7 | HG00408.hp2 HG01099.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.920+2713_920+2717d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | |||||||
chr4:139515492 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.920+2393C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515492 | |||||||
chr4:139515637 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.920+2248T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515637 | |||||||
chr4:139515841 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0270 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.920+2044A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515841 | |||||||
chr4:139515904 | C | G | 3 | a0001c0001t0001g0279 a0001c0001t0031g0226 a0001c0001t0053g0283 |
3 | HG01192.hp1 HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.920+1981G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515904 | |||||||
chr4:139515931 | T | G | 3 | a0001c0001t0011g0144 a0001c0001t0011g0187 a0001c0001t0011g0188 |
3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.920+1954A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515931 | |||||||
chr4:139515947 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.920+1938T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515947 | |||||||
chr4:139516236 | C | T | 3 | a0001c0001t0001g0146 a0002c0003t0001g0048 a0002c0003t0001g0120 |
3 | HG00099.hp2 HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.920+1649G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516236 | |||||||
chr4:139516290 | AC | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.920+1594delG | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516290 | |||||||
chr4:139516326 | C | G | 8 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0049g0235 others(5): Show |
9 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+1559G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516326 | |||||||
chr4:139516332 | G | A | 15 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0045 others(12): Show |
17 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.920+1553C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516332 | |||||||
chr4:139516465 | CA | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
10 | HG01109.hp1 HG01192.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+1419delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516465 | |||||||
chr4:139516465 | CAA | C | 155 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(152): Show |
166 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.920+1418_920+1419d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516465 | |||||||
chr4:139516465 | CAAA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.920+1417_920+1419d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516465 | |||||||
chr4:139516481 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0114 |
3 | HG01496.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.920+1404T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516481 | |||||||
chr4:139516672 | T | A | 9 | a0001c0001t0007g0278 a0001c0001t0013g0007 a0001c0001t0013g0056 others(6): Show |
10 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+1213A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516672 | |||||||
chr4:139516673 | A | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0279 others(15): Show |
20 | HG01175.hp2 HG01192.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.920+1212T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516673 | |||||||
chr4:139516674 | A | T | 1 | a0001c0001t0011g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+1211T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516674 | |||||||
chr4:139516879 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.920+1006G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516879 | |||||||
chr4:139516936 | G | C | 1 | a0001c0001t0011g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+949C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516936 | |||||||
chr4:139516961 | T | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0222 a0001c0001t0001g0275 |
3 | HG02080.hp1 NA18952.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.920+924A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516961 | |||||||
chr4:139517055 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.920+830T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517055 | |||||||
chr4:139517094 | G | C | 1 | a0001c0001t0027g0050 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.920+791C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517094 | |||||||
chr4:139517124 | G | C | 1 | a0001c0001t0049g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.920+761C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517124 | |||||||
chr4:139517193 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.920+692C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517193 | |||||||
chr4:139517232 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.920+653A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517232 | |||||||
chr4:139517475 | CA | C | 34 | a0001c0001t0001g0279 a0001c0001t0002g0005 a0001c0001t0002g0014 others(31): Show |
38 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.920+409delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | |||||||
chr4:139517475 | CAA | C | 16 | a0001c0001t0007g0278 a0001c0001t0012g0227 a0001c0001t0012g0229 others(13): Show |
17 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.920+408_920+409del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | |||||||
chr4:139517475 | CAAA | C | 8 | a0001c0001t0003g0004 a0001c0001t0003g0106 a0001c0001t0003g0185 others(5): Show |
10 | HG01884.hp1 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+407_920+409del others(3): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | |||||||
chr4:139517475 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.920+396_920+409del others(14): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | |||||||
chr4:139517475 | CAAAAAAA others(8): Show |
C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.920+395_920+409del others(15): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | |||||||
chr4:139517475 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.920+394_920+409del others(16): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | |||||||
chr4:139517571 | T | G | 1 | a0001c0001t0011g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+314A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517571 | |||||||
chr4:139517586 | C | T | 12 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0045 others(9): Show |
14 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.920+299G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517586 | |||||||
chr4:139517587 | G | A | 1 | a0001c0001t0017g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.920+298C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517587 | |||||||
chr4:139517612 | G | A | 16 | a0001c0001t0007g0278 a0001c0001t0012g0227 a0001c0001t0012g0229 others(13): Show |
17 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.920+273C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517612 | |||||||
chr4:139517722 | G | A | 3 | a0001c0001t0011g0144 a0001c0001t0011g0187 a0001c0001t0011g0188 |
3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.920+163C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517722 | |||||||
chr4:139517753 | C | T | 14 | a0001c0001t0007g0278 a0001c0001t0012g0227 a0001c0001t0012g0229 others(11): Show |
15 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.920+132G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517753 | |||||||
chr4:139517858 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.920+27C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517858 | |||||||
chr4:139518162 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0190 a0001c0001t0050g0205 |
3 | HG01978.hp1 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.763-120G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518162 | |||||||
chr4:139518177 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0270 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.763-135C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518177 | |||||||
chr4:139518190 | G | A | 4 | a0001c0001t0012g0227 a0001c0001t0012g0229 a0001c0001t0057g0228 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.763-148C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518190 | |||||||
chr4:139518232 | G | A | 3 | a0001c0001t0001g0247 a0001c0002t0001g0208 a0001c0002t0001g0209 |
3 | NA18970.hp1 NA18998.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.763-190C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518232 | |||||||
chr4:139518326 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.763-284T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518326 | |||||||
chr4:139518357 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.763-315C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518357 | |||||||
chr4:139519064 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.763-1022A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139519064 | |||||||
chr4:139519338 | T | C | 3 | a0001c0001t0012g0227 a0001c0001t0057g0228 a0001c0004t0012g0250 |
3 | HG02717.hp1 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.762+939A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139519338 | |||||||
chr4:139520104 | T | TA | 13 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(10): Show |
14 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.762+172dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139520104 | |||||||
chr4:139520423 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0202 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.645-29G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520423 | |||||||
chr4:139520540 | A | T | 1 | a0001c0001t0015g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.645-146T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520540 | |||||||
chr4:139520712 | T | C | 16 | a0001c0001t0001g0285 a0001c0001t0004g0199 a0001c0001t0004g0200 others(13): Show |
17 | HG01361.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.645-318A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520712 | |||||||
chr4:139520718 | C | G | 3 | a0001c0001t0001g0285 a0001c0001t0014g0055 a0001c0001t0049g0235 |
3 | HG01496.hp1 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.645-324G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520718 | |||||||
chr4:139520857 | T | C | 1 | a0001c0001t0006g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.645-463A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520857 | |||||||
chr4:139520991 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.645-597T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520991 | |||||||
chr4:139521151 | C | T | 2 | a0001c0001t0009g0145 a0001c0001t0053g0283 |
2 | HG01192.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.645-757G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521151 | |||||||
chr4:139521197 | G | A | 41 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(38): Show |
44 | HG00423.hp1 HG00735.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.645-803C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521197 | |||||||
chr4:139521271 | C | CA | 14 | a0001c0001t0001g0044 a0001c0001t0006g0006 a0001c0001t0006g0031 others(11): Show |
15 | HG00642.hp2 HG01074.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.645-878dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521271 | |||||||
chr4:139521290 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0015g0211 a0001c0001t0015g0241 others(3): Show |
6 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-896C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521290 | |||||||
chr4:139521319 | G | T | 13 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(10): Show |
14 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.645-925C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521319 | |||||||
chr4:139521354 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.645-960G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521354 | |||||||
chr4:139521407 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-1013G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521407 | |||||||
chr4:139521426 | TA | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.645-1033delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521426 | |||||||
chr4:139521593 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.645-1199G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521593 | |||||||
chr4:139521910 | G | C | 1 | a0001c0001t0014g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.644+1444C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521910 | |||||||
chr4:139521921 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.644+1433G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521921 | |||||||
chr4:139522190 | G | C | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.644+1164C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522190 | |||||||
chr4:139522362 | G | A | 41 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(38): Show |
44 | HG00423.hp1 HG00735.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.644+992C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522362 | |||||||
chr4:139522411 | C | T | 8 | a0001c0001t0005g0009 a0001c0001t0005g0061 a0001c0001t0005g0062 others(5): Show |
9 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.644+943G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522411 | |||||||
chr4:139522493 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0043g0255 a0001c0001t0048g0085 |
4 | HG01074.hp1 HG01192.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+861A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522493 | |||||||
chr4:139522662 | G | A | 1 | a0001c0002t0001g0209 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.644+692C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522662 | |||||||
chr4:139522662 | G | C | 1 | a0001c0001t0055g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.644+692C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522662 | |||||||
chr4:139522741 | C | CT | 11 | a0001c0001t0006g0006 a0001c0001t0007g0278 a0001c0001t0013g0007 others(8): Show |
13 | HG01515.hp2 HG01517.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.644+612dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | |||||||
chr4:139522741 | C | CTT | 42 | a0001c0001t0001g0044 a0001c0001t0001g0212 a0001c0001t0001g0220 others(39): Show |
44 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.644+611_644+612dup others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | |||||||
chr4:139522741 | C | CTTT | 9 | a0001c0001t0001g0020 a0001c0001t0001g0073 a0001c0001t0001g0125 others(6): Show |
10 | HG01175.hp1 HG01361.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.644+610_644+612dup others(3): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | |||||||
chr4:139522741 | CT | C | 109 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(106): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.644+612delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | |||||||
chr4:139522741 | CTT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.644+611_644+612del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | |||||||
chr4:139522741 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0015g0211 a0001c0001t0028g0214 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.644+601_644+612del others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | |||||||
chr4:139522808 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.644+546G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522808 | |||||||
chr4:139522870 | C | T | 17 | a0001c0001t0001g0073 a0001c0001t0001g0212 a0001c0001t0001g0247 others(14): Show |
19 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.644+484G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522870 | |||||||
chr4:139523025 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.644+329T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139523025 | |||||||
chr4:139523604 | G | A | 1 | a0001c0001t0032g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.563-169C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139523604 | |||||||
chr4:139523729 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.563-294C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139523729 | |||||||
chr4:139523832 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.563-397T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139523832 | |||||||
chr4:139524256 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0203 |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-821G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524256 | |||||||
chr4:139524344 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.563-909C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524344 | |||||||
chr4:139524553 | G | C | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.563-1118C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524553 | |||||||
chr4:139524687 | T | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0169 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.563-1252A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524687 | |||||||
chr4:139524816 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0262 |
2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.563-1381G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524816 | |||||||
chr4:139524851 | C | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0203 |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-1416G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524851 | |||||||
chr4:139524925 | T | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.563-1490A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524925 | |||||||
chr4:139525146 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.563-1711A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525146 | |||||||
chr4:139525210 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.563-1775T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525210 | |||||||
chr4:139525239 | G | A | 18 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0125 others(15): Show |
19 | HG01496.hp1 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.563-1804C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525239 | |||||||
chr4:139525263 | G | T | 2 | a0001c0001t0003g0185 a0001c0001t0003g0186 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.563-1828C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525263 | |||||||
chr4:139525337 | C | G | 2 | a0001c0001t0011g0187 a0001c0001t0011g0188 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.563-1902G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525337 | |||||||
chr4:139525375 | C | T | 1 | a0001c0001t0047g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.563-1940G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525375 | |||||||
chr4:139525428 | C | T | 2 | a0001c0002t0001g0210 a0001c0002t0010g0207 |
2 | NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.563-1993G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525428 | |||||||
chr4:139525524 | T | TA | 11 | a0001c0001t0001g0220 a0001c0001t0001g0242 a0001c0001t0001g0243 others(8): Show |
11 | HG01496.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.563-2090dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525524 | |||||||
chr4:139525574 | C | A | 1 | a0001c0002t0006g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.563-2139G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525574 | |||||||
chr4:139525613 | G | GAATTA | 3 | a0001c0004t0001g0251 a0001c0004t0012g0250 a0001c0004t0033g0070 |
3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.563-2183_563-2179d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525613 | |||||||
chr4:139525732 | T | C | 4 | a0001c0001t0008g0026 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02040.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-2297A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525732 | |||||||
chr4:139525738 | G | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.563-2303C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525738 | |||||||
chr4:139525763 | C | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(9): Show |
16 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.563-2328G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525763 | |||||||
chr4:139525930 | A | G | 21 | a0001c0001t0001g0073 a0001c0001t0001g0212 a0001c0001t0001g0247 others(18): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.563-2495T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525930 | |||||||
chr4:139525951 | A | C | 104 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(101): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.563-2516T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525951 | |||||||
chr4:139525983 | C | T | 55 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(52): Show |
56 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.563-2548G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525983 | |||||||
chr4:139526044 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.563-2609C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526044 | |||||||
chr4:139526046 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.563-2611A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526046 | |||||||
chr4:139526046 | T | TTTTGTTT others(1): Show |
3 | a0001c0001t0020g0237 a0001c0005t0054g0282 a0001c0005t0058g0281 |
3 | HG02965.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.563-2619_563-2612d others(10): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526046 | |||||||
chr4:139526046 | TTTTG | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.563-2615_563-2612d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526046 | |||||||
chr4:139526200 | T | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.563-2765A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526200 | |||||||
chr4:139526274 | A | AT | 20 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0233 others(17): Show |
21 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.562+2756dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526274 | |||||||
chr4:139526274 | AT | A | 8 | a0001c0001t0001g0118 a0001c0001t0001g0128 a0001c0001t0001g0181 others(5): Show |
8 | HG00323.hp1 HG00323.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.562+2756delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526274 | |||||||
chr4:139526291 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.562+2740T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526291 | |||||||
chr4:139526407 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.562+2624A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526407 | |||||||
chr4:139526436 | A | AT | 43 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0059 others(40): Show |
44 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.562+2594dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526436 | |||||||
chr4:139526436 | A | ATTT | 14 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0001t0001g0152 others(11): Show |
14 | HG01934.hp2 HG02056.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.562+2592_562+2594d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526436 | |||||||
chr4:139526436 | AT | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.562+2594delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526436 | |||||||
chr4:139526946 | A | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.562+2085T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526946 | |||||||
chr4:139527130 | A | G | 1 | a0001c0001t0032g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562+1901T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527130 | |||||||
chr4:139527435 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.562+1596C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527435 | |||||||
chr4:139527465 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.562+1566C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527465 | |||||||
chr4:139527477 | G | C | 39 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(36): Show |
41 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.562+1554C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527477 | |||||||
chr4:139527619 | A | G | 14 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(11): Show |
15 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.562+1412T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527619 | |||||||
chr4:139528071 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0031g0226 a0001c0001t0053g0283 |
3 | HG01192.hp1 HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.562+960T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528071 | |||||||
chr4:139528251 | C | T | 1 | a0001c0001t0014g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562+780G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528251 | |||||||
chr4:139528266 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.562+765A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528266 | |||||||
chr4:139528310 | G | A | 1 | a0001c0001t0049g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.562+721C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528310 | |||||||
chr4:139528495 | T | C | 67 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0041 others(64): Show |
70 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.562+536A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528495 | |||||||
chr4:139528670 | T | C | 64 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0022 others(61): Show |
69 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.562+361A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528670 | |||||||
chr4:139528844 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0262 |
2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.562+187G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528844 | |||||||
chr4:139528923 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.562+108C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528923 | |||||||
chr4:139529270 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0212 a0001c0001t0001g0247 others(1): Show |
4 | HG02074.hp2 NA18948.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-50C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529270 | |||||||
chr4:139529301 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.373-81C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529301 | |||||||
chr4:139529350 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.373-130G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529350 | |||||||
chr4:139529492 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.373-272G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529492 | |||||||
chr4:139529627 | C | T | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.373-407G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529627 | |||||||
chr4:139529730 | C | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0285 a0001c0001t0014g0055 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-510G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529730 | |||||||
chr4:139529892 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.373-672A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529892 | |||||||
chr4:139529919 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0101 |
3 | NA18974.hp2 NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.373-699G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529919 | |||||||
chr4:139529979 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.373-759G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529979 | |||||||
chr4:139530082 | G | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.373-862C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530082 | |||||||
chr4:139530165 | T | C | 11 | a0001c0001t0001g0025 a0001c0001t0001g0233 a0001c0001t0039g0256 others(8): Show |
11 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.373-945A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530165 | |||||||
chr4:139530223 | G | A | 40 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0022 others(37): Show |
42 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.373-1003C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530223 | |||||||
chr4:139530235 | A | G | 7 | a0001c0001t0001g0044 a0001c0001t0001g0285 a0001c0001t0014g0055 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-1015T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530235 | |||||||
chr4:139530356 | CTT | C | 49 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(46): Show |
51 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.373-1138_373-1137d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | |||||||
chr4:139530356 | CTTT | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.373-1139_373-1137d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | |||||||
chr4:139530356 | CTTTT | C | 66 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0041 others(63): Show |
69 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.373-1140_373-1137d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | |||||||
chr4:139530356 | CTTTTT | C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0147 others(14): Show |
18 | HG00438.hp1 HG01192.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.373-1141_373-1137d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | |||||||
chr4:139530356 | CTTTTTT | C | 20 | a0001c0001t0001g0044 a0001c0001t0001g0073 a0001c0001t0001g0212 others(17): Show |
23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.373-1142_373-1137d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | |||||||
chr4:139530359 | T | C | 1 | a0001c0001t0052g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.373-1139A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530359 | |||||||
chr4:139530395 | TG | T | 41 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0022 others(38): Show |
43 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.373-1176delC | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530395 | |||||||
chr4:139530398 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.373-1178T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530398 | |||||||
chr4:139530690 | C | T | 1 | a0001c0001t0032g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.373-1470G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530690 | |||||||
chr4:139530691 | A | C | 1 | a0001c0001t0002g0116 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.373-1471T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530691 | |||||||
chr4:139530933 | C | T | 130 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(127): Show |
135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.373-1713G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530933 | |||||||
chr4:139531106 | A | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0099 a0001c0001t0042g0098 |
3 | HG00597.hp1 HG02083.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.373-1886T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531106 | |||||||
chr4:139531251 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0125 others(9): Show |
14 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+1914C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531251 | |||||||
chr4:139531400 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.372+1765G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531400 | |||||||
chr4:139531487 | C | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0218 others(3): Show |
7 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1678G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531487 | |||||||
chr4:139531613 | T | C | 72 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0041 others(69): Show |
74 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.372+1552A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531613 | |||||||
chr4:139531669 | T | G | 56 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.372+1496A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531669 | |||||||
chr4:139531752 | C | T | 1 | a0001c0002t0010g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.372+1413G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531752 | |||||||
chr4:139531808 | C | T | 6 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0242 others(3): Show |
6 | HG02004.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+1357G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531808 | |||||||
chr4:139531842 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG00408.hp2 HG00597.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.372+1323C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531842 | |||||||
chr4:139531950 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.372+1215G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531950 | |||||||
chr4:139531951 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.372+1214C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531951 | |||||||
chr4:139531957 | A | G | 113 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(110): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.372+1208T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531957 | |||||||
chr4:139532008 | C | T | 1 | a0001c0001t0038g0221 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.372+1157G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532008 | |||||||
chr4:139532043 | G | A | 1 | a0001c0001t0053g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.372+1122C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532043 | |||||||
chr4:139532079 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0180 a0001c0001t0002g0121 others(2): Show |
5 | HG00280.hp1 HG02257.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1086C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532079 | |||||||
chr4:139532215 | G | T | 26 | a0001c0001t0001g0073 a0001c0001t0001g0178 a0001c0001t0001g0212 others(23): Show |
30 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.372+950C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532215 | |||||||
chr4:139532329 | C | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0220 others(12): Show |
16 | HG01361.hp1 HG02004.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+836G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532329 | |||||||
chr4:139532336 | G | A | 102 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(99): Show |
109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.372+829C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532336 | |||||||
chr4:139532378 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.372+787C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532378 | |||||||
chr4:139532394 | G | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0045 others(6): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+771C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532394 | |||||||
chr4:139532496 | T | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(108): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.372+669A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532496 | |||||||
chr4:139532574 | A | G | 1 | a0001c0001t0052g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.372+591T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532574 | |||||||
chr4:139532660 | TC | T | 14 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0242 others(11): Show |
15 | HG01361.hp1 HG02004.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.372+504delG | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532660 | |||||||
chr4:139532764 | T | C | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+401A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532764 | |||||||
chr4:139532777 | T | C | 1 | a0001c0001t0056g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.372+388A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532777 | |||||||
chr4:139532787 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.372+378C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532787 | |||||||
chr4:139532910 | A | C | 15 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0220 others(12): Show |
16 | HG01361.hp1 HG02004.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+255T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532910 | |||||||
chr4:139533033 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.372+132T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139533033 | |||||||
chr4:139533142 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.372+23C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139533142 | |||||||
chr4:139533557 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.171-191G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533557 | |||||||
chr4:139533564 | T | G | 8 | a0001c0001t0005g0009 a0001c0001t0005g0061 a0001c0001t0005g0062 others(5): Show |
9 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.171-198A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533564 | |||||||
chr4:139533770 | G | C | 1 | a0001c0001t0005g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.171-404C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533770 | |||||||
chr4:139533892 | G | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG00423.hp1 HG01257.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.171-526C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533892 | |||||||
chr4:139533908 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.171-542T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533908 | |||||||
chr4:139533965 | C | CTATG | 11 | a0001c0001t0001g0206 a0001c0001t0002g0005 a0001c0001t0002g0014 others(8): Show |
14 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.171-603_171-600dup others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533965 | |||||||
chr4:139533965 | C | G | 7 | a0001c0001t0004g0184 a0001c0001t0020g0237 a0001c0001t0031g0226 others(4): Show |
7 | HG01192.hp1 HG02055.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-599G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533965 | |||||||
chr4:139533965 | CTATG | C | 7 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0242 others(4): Show |
7 | HG02486.hp2 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-603_171-600del others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533965 | |||||||
chr4:139533982 | T | G | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-616A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533982 | |||||||
chr4:139533986 | T | C | 65 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(62): Show |
66 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.171-620A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533986 | |||||||
chr4:139533993 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.171-627T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533993 | |||||||
chr4:139534100 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.171-734G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534100 | |||||||
chr4:139534199 | A | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0125 others(5): Show |
9 | HG02145.hp1 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.171-833T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534199 | |||||||
chr4:139534320 | G | C | 1 | a0001c0001t0052g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.171-954C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534320 | |||||||
chr4:139534374 | A | C | 145 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(142): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.171-1008T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534374 | |||||||
chr4:139534459 | C | T | 5 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0001g0242 others(2): Show |
5 | HG02486.hp2 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.171-1093G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534459 | |||||||
chr4:139534498 | C | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0289 a0001c0001t0014g0055 |
3 | HG01891.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.171-1132G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534498 | |||||||
chr4:139534609 | C | T | 8 | a0001c0001t0005g0009 a0001c0001t0005g0061 a0001c0001t0005g0062 others(5): Show |
9 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.171-1243G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534609 | |||||||
chr4:139534712 | G | A | 3 | a0001c0004t0001g0251 a0001c0004t0012g0250 a0001c0004t0033g0070 |
3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.171-1346C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534712 | |||||||
chr4:139534789 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG01934.hp1 HG01943.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1423G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534789 | |||||||
chr4:139534797 | G | A | 1 | a0001c0001t0014g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.171-1431C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534797 | |||||||
chr4:139534876 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0271 |
2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.171-1510A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534876 | |||||||
chr4:139534952 | A | C | 9 | a0001c0001t0004g0184 a0001c0001t0015g0211 a0001c0001t0015g0241 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-1586T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534952 | |||||||
chr4:139535085 | T | C | 9 | a0001c0001t0004g0184 a0001c0001t0015g0211 a0001c0001t0015g0241 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-1719A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535085 | |||||||
chr4:139535186 | ATG | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0044 others(14): Show |
19 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.171-1822_171-1821d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535186 | |||||||
chr4:139535407 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.171-2041A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535407 | |||||||
chr4:139535418 | T | C | 1 | a0001c0001t0034g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.171-2052A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535418 | |||||||
chr4:139535534 | A | C | 9 | a0001c0001t0004g0184 a0001c0001t0015g0211 a0001c0001t0015g0241 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-2168T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535534 | |||||||
chr4:139535538 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.171-2172C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535538 | |||||||
chr4:139535708 | T | C | 67 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(64): Show |
68 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.171-2342A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535708 | |||||||
chr4:139535887 | TA | T | 3 | a0001c0001t0008g0026 a0001c0001t0008g0267 a0001c0001t0008g0268 |
3 | HG02040.hp1 NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.171-2522delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535887 | |||||||
chr4:139535930 | A | G | 17 | a0001c0001t0001g0073 a0001c0001t0001g0178 a0001c0001t0001g0212 others(14): Show |
21 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.171-2564T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535930 | |||||||
chr4:139536114 | C | T | 4 | a0001c0001t0001g0178 a0001c0001t0007g0278 a0001c0001t0013g0007 others(1): Show |
5 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-2748G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536114 | |||||||
chr4:139536147 | C | T | 1 | a0001c0001t0029g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171-2781G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536147 | |||||||
chr4:139536253 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.171-2887G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536253 | |||||||
chr4:139536276 | G | T | 95 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(92): Show |
103 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.171-2910C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536276 | |||||||
chr4:139536517 | C | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.171-3151G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536517 | |||||||
chr4:139536709 | TA | T | 4 | a0001c0001t0001g0178 a0001c0001t0007g0278 a0001c0001t0013g0007 others(1): Show |
5 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3344delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536709 | |||||||
chr4:139536725 | T | C | 1 | a0001c0006t0045g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.171-3359A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536725 | |||||||
chr4:139536743 | C | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3377G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536743 | |||||||
chr4:139536752 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0011g0187 a0001c0001t0011g0188 |
4 | HG02109.hp1 HG02559.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.171-3386G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536752 | |||||||
chr4:139536756 | C | T | 1 | a0001c0006t0045g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.171-3390G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536756 | |||||||
chr4:139536757 | C | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3391G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536757 | |||||||
chr4:139536761 | T | TG | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3396dupC | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536761 | |||||||
chr4:139536769 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3403C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536769 | |||||||
chr4:139536773 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3407G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536773 | |||||||
chr4:139536777 | A | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3411T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536777 | |||||||
chr4:139536783 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3417T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536783 | |||||||
chr4:139536785 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3419G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536785 | |||||||
chr4:139536791 | T | C | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3425A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536791 | |||||||
chr4:139536797 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3431T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536797 | |||||||
chr4:139536801 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3435C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536801 | |||||||
chr4:139536803 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3437T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536803 | |||||||
chr4:139536849 | A | G | 3 | a0001c0001t0015g0211 a0001c0001t0015g0241 a0001c0001t0028g0214 |
3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.171-3483T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536849 | |||||||
chr4:139536957 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.171-3591G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536957 | |||||||
chr4:139537067 | C | T | 2 | a0001c0001t0003g0106 a0001c0001t0003g0196 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171-3701G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537067 | |||||||
chr4:139537108 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.171-3742G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537108 | |||||||
chr4:139537122 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.171-3756G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537122 | |||||||
chr4:139537137 | A | G | 154 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(151): Show |
163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.171-3771T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537137 | |||||||
chr4:139537163 | C | T | 1 | a0001c0001t0011g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.171-3797G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537163 | |||||||
chr4:139537289 | T | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3923A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537289 | |||||||
chr4:139537307 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.171-3941C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537307 | |||||||
chr4:139537317 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.171-3951A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537317 | |||||||
chr4:139537484 | C | CA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.171-4119dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537484 | |||||||
chr4:139537485 | A | C | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.171-4119T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537485 | |||||||
chr4:139537518 | C | T | 41 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(38): Show |
43 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.171-4152G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537518 | |||||||
chr4:139537826 | G | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0289 a0001c0001t0014g0055 |
3 | HG01891.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.171-4460C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537826 | |||||||
chr4:139537901 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0083 a0001c0001t0001g0091 others(3): Show |
7 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.171-4535G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537901 | |||||||
chr4:139538017 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.171-4651C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538017 | |||||||
chr4:139538105 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.171-4739A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538105 | |||||||
chr4:139538106 | T | C | 1 | a0001c0001t0035g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.171-4740A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538106 | |||||||
chr4:139538172 | G | T | 1 | a0001c0001t0021g0079 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.171-4806C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538172 | |||||||
chr4:139538203 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.171-4837T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538203 | |||||||
chr4:139538484 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.171-5118G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538484 | |||||||
chr4:139538548 | C | G | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.171-5182G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538548 | |||||||
chr4:139538548 | C | T | 1 | a0001c0001t0011g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.171-5182G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538548 | |||||||
chr4:139538568 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.171-5202T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538568 | |||||||
chr4:139538574 | C | T | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-5208G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538574 | |||||||
chr4:139538630 | T | C | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-5264A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538630 | |||||||
chr4:139538697 | T | TACATAAT others(329): Show |
1 | a0001c0001t0052g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.171-5332_171-5331i others(338): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538697 | |||||||
chr4:139538816 | G | A | 1 | a0001c0001t0021g0079 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.171-5450C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538816 | |||||||
chr4:139538996 | T | C | 3 | a0001c0001t0003g0106 a0001c0001t0003g0196 a0001c0001t0032g0084 |
3 | HG02886.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171-5630A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538996 | |||||||
chr4:139539002 | T | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0148 others(1): Show |
4 | HG01257.hp1 HG01943.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-5636A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539002 | |||||||
chr4:139539149 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.171-5783G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539149 | |||||||
chr4:139539164 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0202 others(2): Show |
6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-5798C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539164 | |||||||
chr4:139539473 | C | T | 2 | a0001c0001t0016g0261 a0001c0001t0016g0263 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.171-6107G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539473 | |||||||
chr4:139539502 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.171-6136A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539502 | |||||||
chr4:139539669 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0155 a0001c0001t0001g0169 others(3): Show |
7 | HG00558.hp2 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.171-6303G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539669 | |||||||
chr4:139540023 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0202 others(2): Show |
6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-6657G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540023 | |||||||
chr4:139540118 | C | T | 9 | a0001c0001t0004g0184 a0001c0001t0015g0211 a0001c0001t0015g0241 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-6752G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540118 | |||||||
chr4:139540387 | G | A | 2 | a0001c0001t0044g0049 a0002c0003t0001g0048 |
2 | HG00099.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.170+6533C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540387 | |||||||
chr4:139540405 | G | T | 1 | a0001c0006t0045g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.170+6515C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540405 | |||||||
chr4:139540498 | C | T | 1 | a0001c0001t0032g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.170+6422G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540498 | |||||||
chr4:139540547 | G | C | 1 | a0001c0001t0036g0108 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.170+6373C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540547 | |||||||
chr4:139540563 | A | T | 19 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0044 others(16): Show |
21 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.170+6357T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540563 | |||||||
chr4:139540660 | G | A | 18 | a0001c0001t0001g0073 a0001c0001t0001g0178 a0001c0001t0001g0212 others(15): Show |
22 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.170+6260C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540660 | |||||||
chr4:139540759 | T | C | 10 | a0001c0001t0001g0147 a0001c0001t0004g0184 a0001c0001t0015g0211 others(7): Show |
10 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.170+6161A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540759 | |||||||
chr4:139540961 | A | G | 1 | a0001c0001t0011g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.170+5959T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540961 | |||||||
chr4:139540976 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+5944C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540976 | |||||||
chr4:139541125 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.170+5795C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541125 | |||||||
chr4:139541247 | T | C | 177 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(174): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.170+5673A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541247 | |||||||
chr4:139541272 | G | C | 14 | a0001c0001t0001g0073 a0001c0001t0001g0212 a0001c0001t0001g0245 others(11): Show |
17 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.170+5648C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541272 | |||||||
chr4:139541325 | A | G | 2 | a0001c0001t0016g0261 a0001c0001t0016g0263 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.170+5595T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541325 | |||||||
chr4:139541369 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.170+5551T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541369 | |||||||
chr4:139541503 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+5417C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541503 | |||||||
chr4:139541609 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0035g0023 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.170+5311C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541609 | |||||||
chr4:139541625 | T | G | 178 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(175): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.170+5295A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541625 | |||||||
chr4:139541966 | C | T | 9 | a0001c0001t0004g0232 a0001c0002t0001g0208 a0001c0002t0001g0209 others(6): Show |
9 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.170+4954G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541966 | |||||||
chr4:139541970 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+4950C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541970 | |||||||
chr4:139542012 | A | G | 9 | a0001c0001t0004g0232 a0001c0002t0001g0208 a0001c0002t0001g0209 others(6): Show |
9 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.170+4908T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542012 | |||||||
chr4:139542107 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0109 a0001c0001t0001g0111 others(2): Show |
5 | HG02523.hp2 NA18955.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.170+4813C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542107 | |||||||
chr4:139542127 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+4793A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542127 | |||||||
chr4:139542200 | A | G | 1 | a0001c0001t0006g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.170+4720T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542200 | |||||||
chr4:139542411 | A | G | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+4509T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542411 | |||||||
chr4:139542481 | TA | T | 6 | a0001c0001t0005g0009 a0001c0001t0005g0061 a0001c0001t0005g0062 others(3): Show |
7 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+4438delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542481 | |||||||
chr4:139542503 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.170+4417G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542503 | |||||||
chr4:139542504 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+4416G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542504 | |||||||
chr4:139542554 | C | G | 173 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(170): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.170+4366G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542554 | |||||||
chr4:139542810 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.170+4110C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542810 | |||||||
chr4:139542845 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0202 others(2): Show |
6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.170+4075G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542845 | |||||||
chr4:139542862 | C | G | 1 | a0001c0001t0001g0258 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.170+4058G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542862 | |||||||
chr4:139542940 | T | C | 6 | a0001c0001t0004g0184 a0001c0001t0031g0226 a0001c0001t0053g0283 others(3): Show |
6 | HG01192.hp1 HG02055.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+3980A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542940 | |||||||
chr4:139542962 | C | G | 2 | a0001c0001t0031g0226 a0001c0001t0053g0283 |
2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.170+3958G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542962 | |||||||
chr4:139543111 | C | T | 53 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(50): Show |
54 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.170+3809G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543111 | |||||||
chr4:139543354 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+3566A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543354 | |||||||
chr4:139543539 | A | G | 42 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(39): Show |
44 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.170+3381T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543539 | |||||||
chr4:139543608 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.170+3312A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543608 | |||||||
chr4:139543676 | G | T | 1 | a0001c0006t0045g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.170+3244C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543676 | |||||||
chr4:139543719 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.170+3201T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543719 | |||||||
chr4:139543724 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.170+3196C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543724 | |||||||
chr4:139543727 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.170+3193G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543727 | |||||||
chr4:139543756 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.170+3164A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543756 | |||||||
chr4:139543768 | A | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0086 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.170+3152T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543768 | |||||||
chr4:139543798 | C | CA | 24 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0112 others(21): Show |
25 | HG01106.hp2 HG01261.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+3121dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | |||||||
chr4:139543798 | C | CAA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0147 a0001c0001t0001g0285 others(4): Show |
7 | HG01192.hp1 HG01891.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+3120_170+3121d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | |||||||
chr4:139543798 | C | CAAA | 9 | a0001c0001t0001g0022 a0001c0001t0004g0232 a0001c0001t0047g0191 others(6): Show |
9 | HG02148.hp2 HG02622.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+3119_170+3121d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | |||||||
chr4:139543798 | C | CAAAAA | 38 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(35): Show |
40 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.170+3117_170+3121d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | |||||||
chr4:139543798 | C | CAAAAAA | 63 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0041 others(60): Show |
64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.170+3116_170+3121d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | |||||||
chr4:139543798 | CA | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0090 a0001c0001t0001g0125 others(10): Show |
14 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.170+3121delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | |||||||
chr4:139543824 | CGTGGTG | C | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+3090_170+3095d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543824 | |||||||
chr4:139543857 | A | G | 1 | a0001c0001t0009g0145 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.170+3063T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543857 | |||||||
chr4:139543924 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0262 |
2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.170+2996C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543924 | |||||||
chr4:139543962 | T | TCAAA | 72 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0017 others(69): Show |
77 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.170+2954_170+2957d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543962 | |||||||
chr4:139543962 | T | TCAAACAA others(1): Show |
67 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(64): Show |
71 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.170+2950_170+2957d others(10): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543962 | |||||||
chr4:139543962 | T | TCAAACAA others(5): Show |
8 | a0001c0001t0001g0130 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG00280.hp2 HG01255.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.170+2946_170+2957d others(14): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543962 | |||||||
chr4:139544060 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0212 a0001c0001t0027g0050 |
3 | HG02074.hp2 NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.170+2860C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544060 | |||||||
chr4:139544163 | G | T | 18 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0218 others(15): Show |
20 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.170+2757C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544163 | |||||||
chr4:139544195 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.170+2725C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544195 | |||||||
chr4:139544200 | G | C | 6 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(3): Show |
6 | HG02148.hp2 HG03098.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.170+2720C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544200 | |||||||
chr4:139544274 | C | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(96): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.170+2646G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544274 | |||||||
chr4:139544290 | C | CTAAAA | 31 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0115 others(28): Show |
35 | HG00099.hp1 HG01074.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.170+2625_170+2629d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | C | CTAAAATA others(3): Show |
14 | a0001c0001t0004g0184 a0001c0001t0004g0199 a0001c0001t0004g0200 others(11): Show |
14 | HG01106.hp2 HG01192.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.170+2620_170+2629d others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | C | CTAAAATA others(8): Show |
7 | a0001c0001t0015g0211 a0001c0001t0015g0241 a0001c0001t0020g0021 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+2615_170+2629d others(17): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | C | CTAAAATA others(18): Show |
4 | a0001c0001t0001g0019 a0001c0001t0001g0218 a0001c0006t0018g0066 others(1): Show |
5 | HG00438.hp1 HG01099.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+2605_170+2629d others(27): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | C | CTAAAATA others(23): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0219 |
2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.170+2600_170+2629d others(32): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | CTAAAA | C | 95 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(92): Show |
98 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.170+2625_170+2629d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | CTAAAATA others(3): Show |
C | 8 | a0001c0001t0001g0119 a0001c0001t0001g0180 a0001c0001t0002g0121 others(5): Show |
8 | HG00280.hp1 HG02257.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.170+2620_170+2629d others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544290 | CTAAAATA others(8): Show |
C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0274 |
2 | HG02155.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.170+2615_170+2629d others(17): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | |||||||
chr4:139544362 | GA | G | 6 | a0001c0001t0001g0178 a0001c0001t0007g0176 a0001c0001t0007g0177 others(3): Show |
7 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+2557delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544362 | |||||||
chr4:139544455 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.170+2465C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544455 | |||||||
chr4:139544595 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.170+2325C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544595 | |||||||
chr4:139544797 | A | AGT | 12 | a0001c0001t0001g0065 a0001c0001t0001g0086 a0001c0001t0001g0151 others(9): Show |
14 | HG00323.hp1 HG01109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.170+2121_170+2122d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGT | 2 | a0001c0001t0001g0010 a0001c0001t0048g0085 |
3 | HG01074.hp1 HG01192.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.170+2119_170+2122d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0126 a0001c0001t0001g0142 a0001c0001t0001g0169 |
3 | HG02056.hp1 HG02132.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.170+2115_170+2122d others(10): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGTGTG others(3): Show |
63 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0027 others(60): Show |
65 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.170+2113_170+2122d others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGTGTG others(5): Show |
24 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0131 others(21): Show |
25 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.170+2111_170+2122d others(14): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0182 a0001c0001t0001g0254 a0001c0001t0001g0279 |
3 | HG02083.hp2 HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.170+2109_170+2122d others(16): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0009g0124 a0001c0001t0009g0238 |
2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.170+2107_170+2122d others(18): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | A | AGTGTGTG others(11): Show |
2 | a0001c0001t0009g0145 a0001c0001t0041g0213 |
2 | HG03195.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.170+2105_170+2122d others(20): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | AGT | A | 18 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0218 others(15): Show |
19 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.170+2121_170+2122d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | AGTGT | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0001g0198 others(12): Show |
16 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.170+2119_170+2122d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139544797 | AGTGTGT | A | 41 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0044 others(38): Show |
46 | HG00099.hp1 HG01169.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.170+2117_170+2122d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | |||||||
chr4:139545086 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+1834A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545086 | |||||||
chr4:139545157 | A | G | 167 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(164): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.170+1763T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545157 | |||||||
chr4:139545169 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+1751T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545169 | |||||||
chr4:139545189 | CT | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(12): Show |
16 | HG00735.hp2 HG01071.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.170+1730delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545189 | |||||||
chr4:139545309 | A | G | 6 | a0001c0001t0005g0009 a0001c0001t0005g0061 a0001c0001t0005g0062 others(3): Show |
7 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+1611T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545309 | |||||||
chr4:139545355 | G | A | 1 | a0001c0001t0055g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.170+1565C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545355 | |||||||
chr4:139545450 | C | T | 98 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(95): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.170+1470G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545450 | |||||||
chr4:139545610 | A | G | 1 | a0001c0001t0027g0050 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.170+1310T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545610 | |||||||
chr4:139545613 | C | T | 170 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(167): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.170+1307G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545613 | |||||||
chr4:139545695 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0018g0082 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.170+1225G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545695 | |||||||
chr4:139545767 | C | T | 1 | a0001c0001t0015g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.170+1153G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545767 | |||||||
chr4:139545896 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.170+1024G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545896 | |||||||
chr4:139545959 | ATGGTCAC others(16): Show |
A | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.170+938_170+960del others(23): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545959 | |||||||
chr4:139545968 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.170+952G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545968 | |||||||
chr4:139546077 | CAAGCGAG others(78): Show |
C | 1 | a0001c0001t0009g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170+758_170+842del others(85): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546077 | |||||||
chr4:139546154 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.170+766T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546154 | |||||||
chr4:139546241 | A | G | 3 | a0001c0004t0001g0251 a0001c0004t0012g0250 a0001c0004t0033g0070 |
3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.170+679T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546241 | |||||||
chr4:139546317 | G | A | 6 | a0001c0001t0001g0178 a0001c0001t0007g0176 a0001c0001t0007g0177 others(3): Show |
7 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+603C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546317 | |||||||
chr4:139546394 | C | T | 2 | a0001c0001t0017g0034 a0001c0001t0026g0035 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.170+526G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546394 | |||||||
chr4:139546456 | T | C | 99 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(96): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.170+464A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546456 | |||||||
chr4:139546502 | C | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0206 a0001c0001t0001g0239 others(3): Show |
7 | HG02559.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+418G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546502 | |||||||
chr4:139546604 | A | T | 11 | a0001c0001t0001g0044 a0001c0001t0004g0184 a0001c0001t0015g0211 others(8): Show |
11 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+316T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546604 | |||||||
chr4:139546605 | TGA | T | 11 | a0001c0001t0001g0044 a0001c0001t0004g0184 a0001c0001t0015g0211 others(8): Show |
11 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+313_170+314del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546605 | |||||||
chr4:139547377 | T | C | 1 | a0001c0001t0052g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-328A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547377 | |||||||
chr4:139547382 | A | G | 99 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(96): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-333T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547382 | |||||||
chr4:139547468 | C | T | 3 | a0001c0001t0015g0211 a0001c0001t0015g0241 a0001c0001t0028g0214 |
3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.41-419G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547468 | |||||||
chr4:139547547 | A | G | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-498T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547547 | |||||||
chr4:139547548 | T | A | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-499A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547548 | |||||||
chr4:139547554 | A | T | 1 | a0001c0001t0017g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.41-505T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547554 | |||||||
chr4:139547583 | T | G | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-534A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547583 | |||||||
chr4:139547589 | C | A | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-540G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547589 | |||||||
chr4:139547590 | C | G | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-541G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547590 | |||||||
chr4:139547593 | T | TGATGGAT others(25): Show |
1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-545_41-544insCG others(30): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547593 | |||||||
chr4:139547634 | A | C | 1 | a0001c0001t0016g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-585T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547634 | |||||||
chr4:139547895 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0233 a0001c0001t0004g0232 |
3 | HG02615.hp1 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41-846T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547895 | |||||||
chr4:139548216 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.41-1167T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548216 | |||||||
chr4:139548236 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.41-1187A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548236 | |||||||
chr4:139548459 | C | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(96): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-1410G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548459 | |||||||
chr4:139548501 | G | A | 1 | a0001c0001t0029g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-1452C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548501 | |||||||
chr4:139548567 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-1518C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548567 | |||||||
chr4:139549058 | T | G | 124 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(121): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.41-2009A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549058 | |||||||
chr4:139549115 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.41-2066G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549115 | |||||||
chr4:139549451 | G | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(96): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-2402C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549451 | |||||||
chr4:139549460 | T | C | 13 | a0001c0001t0001g0073 a0001c0001t0001g0212 a0001c0001t0001g0245 others(10): Show |
15 | HG00099.hp1 HG00323.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-2411A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549460 | |||||||
chr4:139549512 | A | ATTCCTTC others(5): Show |
25 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0146 others(22): Show |
27 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.41-2475_41-2464dup others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | |||||||
chr4:139549512 | A | ATTCCTTC others(9): Show |
1 | a0001c0001t0009g0145 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.41-2479_41-2464dup others(16): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | |||||||
chr4:139549512 | A | ATTCCTTC others(13): Show |
42 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0029 others(39): Show |
44 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.41-2464_41-2463ins others(20): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | |||||||
chr4:139549512 | A | ATTCCTTC others(17): Show |
52 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0041 others(49): Show |
53 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.41-2464_41-2463ins others(24): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | |||||||
chr4:139549512 | A | ATTCCTTC others(21): Show |
3 | a0001c0001t0001g0071 a0001c0001t0001g0253 a0001c0001t0029g0189 |
3 | HG03834.hp1 NA18950.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.41-2464_41-2463ins others(28): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | |||||||
chr4:139549512 | A | ATTCCTTC others(29): Show |
1 | a0001c0001t0001g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.41-2464_41-2463ins others(36): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | |||||||
chr4:139549581 | C | T | 2 | a0001c0001t0017g0034 a0001c0001t0026g0035 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.41-2532G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549581 | |||||||
chr4:139549616 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.41-2567T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549616 | |||||||
chr4:139549682 | T | C | 1 | a0001c0001t0055g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.41-2633A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549682 | |||||||
chr4:139549747 | G | C | 3 | a0001c0004t0001g0251 a0001c0004t0012g0250 a0001c0004t0033g0070 |
3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41-2698C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549747 | |||||||
chr4:139549774 | TA | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0125 a0001c0001t0001g0202 others(2): Show |
6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-2726delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549774 | |||||||
chr4:139549785 | A | T | 2 | a0001c0001t0001g0078 a0001c0001t0021g0079 |
2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.41-2736T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549785 | |||||||
chr4:139549892 | C | CTCCACCC others(77): Show |
1 | a0001c0001t0009g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.41-2844_41-2843ins others(84): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549892 | |||||||
chr4:139549907 | A | C | 1 | a0001c0001t0009g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.41-2858T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549907 | |||||||
chr4:139549972 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0011g0187 a0001c0001t0011g0188 |
4 | HG02109.hp1 HG02559.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2923C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549972 | |||||||
chr4:139550094 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.41-3045T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550094 | |||||||
chr4:139550143 | T | C | 23 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0178 others(20): Show |
27 | HG00099.hp1 HG00323.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.41-3094A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550143 | |||||||
chr4:139550165 | C | G | 6 | a0001c0001t0005g0009 a0001c0001t0005g0061 a0001c0001t0005g0062 others(3): Show |
7 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-3116G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550165 | |||||||
chr4:139550370 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.41-3321T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550370 | |||||||
chr4:139550396 | T | C | 173 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(170): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.41-3347A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550396 | |||||||
chr4:139550909 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-3860A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550909 | |||||||
chr4:139551000 | C | G | 3 | a0001c0004t0001g0251 a0001c0004t0012g0250 a0001c0004t0033g0070 |
3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41-3951G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551000 | |||||||
chr4:139551032 | A | G | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-3983T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551032 | |||||||
chr4:139551127 | G | A | 178 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(175): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.41-4078C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551127 | |||||||
chr4:139551299 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0047g0191 |
2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.41-4250T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551299 | |||||||
chr4:139551402 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.41-4353T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551402 | |||||||
chr4:139551524 | A | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG01433.hp1 HG01516.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4475T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551524 | |||||||
chr4:139551579 | A | C | 1 | a0001c0001t0002g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.40+4519T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551579 | |||||||
chr4:139551640 | G | GAGCTGAC others(163): Show |
1 | a0001c0001t0011g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+4457_40+4458ins others(170): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551640 | |||||||
chr4:139551737 | T | C | 1 | a0001c0001t0014g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+4361A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551737 | |||||||
chr4:139551742 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.40+4356G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551742 | |||||||
chr4:139551743 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.40+4355C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551743 | |||||||
chr4:139551836 | C | G | 4 | a0001c0001t0055g0231 a0001c0004t0001g0251 a0001c0004t0012g0250 others(1): Show |
4 | HG02717.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+4262G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551836 | |||||||
chr4:139551841 | T | C | 1 | a0001c0001t0041g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.40+4257A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551841 | |||||||
chr4:139551853 | A | C | 1 | a0001c0001t0056g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.40+4245T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551853 | |||||||
chr4:139551897 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.40+4201C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551897 | |||||||
chr4:139552045 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.40+4053C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552045 | |||||||
chr4:139552052 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.40+4046G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552052 | |||||||
chr4:139552077 | A | C | 6 | a0001c0001t0004g0184 a0001c0001t0015g0241 a0001c0001t0028g0214 others(3): Show |
6 | HG02486.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+4021T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552077 | |||||||
chr4:139552132 | G | A | 98 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0042 others(95): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.40+3966C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552132 | |||||||
chr4:139552209 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0220 a0001c0001t0001g0242 others(3): Show |
7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+3889C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552209 | |||||||
chr4:139552487 | G | T | 45 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0071 others(42): Show |
49 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.40+3611C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552487 | |||||||
chr4:139552552 | GC | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0279 a0001c0001t0003g0004 others(9): Show |
15 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+3545delG | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552552 | |||||||
chr4:139552659 | T | C | 12 | a0001c0001t0001g0047 a0001c0001t0001g0245 a0001c0001t0002g0005 others(9): Show |
14 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+3439A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552659 | |||||||
chr4:139552695 | C | T | 3 | a0001c0001t0012g0227 a0001c0001t0012g0229 a0001c0001t0057g0228 |
3 | HG02258.hp1 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.40+3403G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552695 | |||||||
chr4:139552784 | C | T | 4 | a0001c0001t0007g0278 a0001c0001t0013g0007 a0001c0001t0013g0056 others(1): Show |
5 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+3314G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552784 | |||||||
chr4:139552790 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.40+3308C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552790 | |||||||
chr4:139553073 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG00408.hp2 HG00597.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.40+3025C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553073 | |||||||
chr4:139553240 | A | G | 2 | a0001c0001t0031g0226 a0001c0001t0053g0283 |
2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.40+2858T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553240 | |||||||
chr4:139553260 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.40+2838A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553260 | |||||||
chr4:139553467 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.40+2631A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553467 | |||||||
chr4:139553541 | A | G | 1 | a0001c0001t0053g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+2557T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553541 | |||||||
chr4:139553703 | G | A | 1 | a0001c0001t0034g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.40+2395C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553703 | |||||||
chr4:139553889 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.40+2209A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553889 | |||||||
chr4:139553919 | C | G | 1 | a0001c0001t0004g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.40+2179G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553919 | |||||||
chr4:139554846 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.40+1252G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139554846 | |||||||
chr4:139555060 | G | T | 86 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(83): Show |
95 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.40+1038C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555060 | |||||||
chr4:139555121 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.40+977T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555121 | |||||||
chr4:139555182 | C | CA | 109 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(106): Show |
114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.40+915dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555182 | |||||||
chr4:139555182 | CA | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(27): Show |
34 | HG00621.hp1 HG01175.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+915delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555182 | |||||||
chr4:139555182 | CAAAAAA | C | 15 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0046 others(12): Show |
17 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.40+910_40+915delTT others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555182 | |||||||
chr4:139555186 | A | C | 5 | a0001c0001t0001g0279 a0001c0001t0004g0280 a0001c0001t0007g0278 others(2): Show |
5 | HG02886.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+912T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555186 | |||||||
chr4:139555355 | G | A | 1 | a0001c0001t0003g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.40+743C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555355 | |||||||
chr4:139555438 | C | T | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(17): Show |
20 | HG00408.hp1 HG01106.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.40+660G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555438 | |||||||
chr4:139555477 | G | A | 32 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(29): Show |
32 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+621C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555477 | |||||||
chr4:139555493 | C | A | 6 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0289 others(3): Show |
6 | HG01069.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+605G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555493 | |||||||
chr4:139555826 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.40+272T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555826 | |||||||
chr4:139555977 | C | A | 13 | a0001c0001t0001g0020 a0001c0001t0001g0279 a0001c0001t0001g0285 others(10): Show |
14 | HG01069.hp1 HG01192.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.40+121G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555977 | |||||||
chr4:139556004 | C | T | 1 | a0001c0001t0020g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+94G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139556004 |