Item | Value |
---|---|
geneid | 50804 |
ensemblid | ENSG00000104177.20 |
hgncid | 17940 |
symbol | MYEF2 |
name | myelin expression factor 2 |
refseq_nuc | NM_016132.5 |
refseq_prot | NP_057216.3 |
ensembl_nuc | ENST00000324324.12 |
ensembl_prot | ENSP00000316950.7 |
mane_status | MANE Select |
chr | chr15 |
start | 48134632 |
end | 48178295 |
strand | - |
ver | v1.2 |
region | chr15:48134632-48178295 |
region5000 | chr15:48129632-48183295 |
regionname0 | MYEF2_chr15_48134632_48178295 |
regionname5000 | MYEF2_chr15_48129632_48183295 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 600 | 221 | 66 | 22 | 115 | 0 | 17 | 87 | MYEF2_chr15_48129632_48183295 | MYEF2 | MADAN others(595): Show |
chr15 | 48129632 | 48183295 |
a0002 | 0/0 | 600 | 32 | 13 | 12 | 6 | 0 | 1 | 4 | MYEF2_chr15_48129632_48183295 | MYEF2 | MADAN others(595): Show |
chr15 | 48129632 | 48183295 |
a0003 | 1/0 | 600 | 4 | 2 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | MADAN others(595): Show |
chr15 | 48129632 | 48183295 |
a0004 | 0/0 | 600 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | MYEF2_chr15_48129632_48183295 | MYEF2 | MADAN others(595): Show |
chr15 | 48129632 | 48183295 |
a0005 | 0/0 | 600 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | MADAN others(595): Show |
chr15 | 48129632 | 48183295 |
a0006 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | MADAN others(595): Show |
chr15 | 48129632 | 48183295 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1800 | 221 | 66 | 22 | 115 | 0 | 17 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 | ||
a0002c0002 | 0/0 | 1800 | 31 | 12 | 12 | 6 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 | ||
a0002c0006 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 | ||
a0003c0004 | 1/0 | 1800 | 4 | 2 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 | ||
a0004c0003 | 0/0 | 1800 | 5 | 0 | 0 | 5 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 | ||
a0005c0005 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 | ||
a0006c0007 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATGGC others(1795): Show |
chr15 | 48129632 | 48183295 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10138 | 59 | 11 | 1 | 41 | 0 | 6 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0002 | 0/0 | 10137 | 46 | 5 | 10 | 22 | 0 | 9 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0003 | 0/0 | 10137 | 33 | 14 | 4 | 15 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0005 | 0/0 | 10138 | 13 | 11 | 0 | 2 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0006 | 0/0 | 10138 | 8 | 1 | 3 | 4 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0008 | 0/0 | 10138 | 3 | 3 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0009 | 0/0 | 10137 | 6 | 1 | 0 | 5 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0010 | 0/0 | 10137 | 6 | 0 | 0 | 6 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0011 | 0/0 | 10139 | 5 | 1 | 0 | 4 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10134): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0012 | 0/0 | 10137 | 3 | 0 | 0 | 2 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0014 | 0/0 | 10138 | 3 | 3 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0015 | 0/0 | 10136 | 3 | 0 | 0 | 3 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10131): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0016 | 0/0 | 10138 | 3 | 0 | 2 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0017 | 0/0 | 10137 | 2 | 1 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0018 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0019 | 0/0 | 10137 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0020 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0022 | 0/0 | 10137 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0023 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0028 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0030 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0031 | 0/0 | 10137 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0032 | 0/1 | 10137 | 1 | 0 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0033 | 0/0 | 10137 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0034 | 0/0 | 10138 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0035 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0036 | 0/0 | 10137 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0037 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0038 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0039 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0040 | 0/0 | 10140 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10135): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0041 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0042 | 0/0 | 10138 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0043 | 0/0 | 10139 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10134): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0044 | 0/0 | 10138 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0045 | 0/0 | 10138 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0046 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0047 | 0/0 | 10138 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0048 | 0/0 | 10138 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0049 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0001c0001t0050 | 0/0 | 10137 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0004 | 0/0 | 10135 | 16 | 1 | 8 | 6 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10130): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0007 | 0/0 | 10137 | 7 | 5 | 2 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0013 | 0/0 | 10135 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10130): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0018 | 0/0 | 10137 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0024 | 0/0 | 10135 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10130): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0025 | 0/0 | 10138 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0026 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0027 | 0/0 | 10135 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10130): Show |
chr15 | 48129632 | 48183295 |
a0002c0002t0029 | 0/0 | 10135 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10130): Show |
chr15 | 48129632 | 48183295 |
a0002c0006t0021 | 0/0 | 10137 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0003c0004t0002 | 1/0 | 10137 | 1 | 0 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0003c0004t0008 | 0/0 | 10138 | 3 | 2 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0004c0003t0003 | 0/0 | 10137 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0004c0003t0006 | 0/0 | 10138 | 4 | 0 | 0 | 4 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10133): Show |
chr15 | 48129632 | 48183295 |
a0005c0005t0002 | 0/0 | 10137 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10132): Show |
chr15 | 48129632 | 48183295 |
a0006c0007t0013 | 0/0 | 10135 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | ATTGT others(10130): Show |
chr15 | 48129632 | 48183295 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 7 | 3 | 0 | 3 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0001 | 0/0 | 23 | 3 | 6 | 9 | 0 | 5 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0002 | 0/0 | 13 | 4 | 2 | 7 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0009g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0010g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0010g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0014g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0015g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0016g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0017g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0018g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0019g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0022g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0023g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0028g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0030g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0031g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0032g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0033g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0034g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0035g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0036g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0037g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0038g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0039g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0040g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0041g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0042g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0043g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0044g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0045g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0046g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0047g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0048g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0049g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0001c0001t0050g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0007g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0007g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0013g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0018g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0024g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0025g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0026g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0027g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0002t0029g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0002c0006t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0003c0004t0002g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0003c0004t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0003c0004t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0004c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0004c0003t0006g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0004c0003t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0005c0005t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
a0006c0007t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00408 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00438 | hp1 | a0001 | c0001 | t0044 | g0066 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00544 | hp2 | a0002 | c0002 | t0004 | g0154 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01167 | hp1 | a0002 | c0002 | t0007 | g0033 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01167 | hp2 | a0001 | c0001 | t0017 | g0026 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01169 | hp1 | a0002 | c0002 | t0007 | g0033 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01243 | hp2 | a0002 | c0002 | t0004 | g0051 | AMR | PUR | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01255 | hp2 | a0002 | c0002 | t0024 | g0147 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01257 | hp2 | a0002 | c0002 | t0004 | g0156 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01346 | hp1 | a0002 | c0002 | t0004 | g0031 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01496 | hp1 | a0003 | c0004 | t0008 | g0046 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0049 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01891 | hp1 | a0003 | c0004 | t0008 | g0017 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01928 | hp1 | a0002 | c0002 | t0004 | g0050 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0163 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01934 | hp2 | a0001 | c0001 | t0016 | g0024 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01952 | hp1 | a0002 | c0002 | t0004 | g0031 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01952 | hp2 | a0005 | c0005 | t0002 | g0035 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01975 | hp2 | a0001 | c0001 | t0016 | g0024 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0159 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0028 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0013 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02004 | hp2 | a0001 | c0001 | t0048 | g0169 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02040 | hp2 | a0002 | c0002 | t0004 | g0039 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02055 | hp2 | a0001 | c0001 | t0046 | g0077 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02129 | hp1 | a0001 | c0001 | t0010 | g0075 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02132 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02148 | hp2 | a0002 | c0002 | t0004 | g0013 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0013 | AMR | PEL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02280 | hp1 | a0001 | c0001 | t0035 | g0045 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02615 | hp1 | a0001 | c0001 | t0037 | g0055 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02622 | hp1 | a0001 | c0001 | t0019 | g0018 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02630 | hp1 | a0001 | c0001 | t0040 | g0059 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02647 | hp1 | a0001 | c0001 | t0030 | g0104 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02647 | hp2 | a0002 | c0002 | t0007 | g0015 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02723 | hp1 | a0002 | c0002 | t0004 | g0146 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02723 | hp2 | a0001 | c0001 | t0018 | g0165 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02818 | hp1 | a0001 | c0001 | t0028 | g0120 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02896 | hp1 | a0001 | c0001 | t0019 | g0018 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0132 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0131 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02922 | hp1 | a0001 | c0001 | t0049 | g0123 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0103 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0137 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03017 | hp2 | a0001 | c0001 | t0012 | g0094 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03041 | hp1 | a0002 | c0002 | t0029 | g0142 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03139 | hp1 | a0003 | c0004 | t0008 | g0017 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03139 | hp2 | a0001 | c0001 | t0038 | g0069 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03195 | hp2 | a0002 | c0002 | t0007 | g0144 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03209 | hp2 | a0001 | c0001 | t0039 | g0130 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03225 | hp1 | a0002 | c0002 | t0025 | g0141 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03453 | hp1 | a0001 | c0001 | t0041 | g0079 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03453 | hp2 | a0002 | c0002 | t0007 | g0170 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03486 | hp1 | a0001 | c0001 | t0023 | g0124 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03486 | hp2 | a0006 | c0007 | t0013 | g0148 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03579 | hp1 | a0002 | c0006 | t0021 | g0053 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0155 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03831 | hp1 | a0001 | c0001 | t0022 | g0052 | SAS | BEB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | YRI | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18939 | hp1 | a0001 | c0001 | t0047 | g0065 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18944 | hp2 | a0001 | c0001 | t0009 | g0128 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18947 | hp1 | a0001 | c0001 | t0010 | g0108 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18947 | hp2 | a0001 | c0001 | t0010 | g0021 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18948 | hp2 | a0002 | c0002 | t0004 | g0152 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18949 | hp2 | a0001 | c0001 | t0034 | g0107 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18951 | hp1 | a0001 | c0001 | t0042 | g0085 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18952 | hp1 | a0004 | c0003 | t0006 | g0166 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18953 | hp2 | a0004 | c0003 | t0006 | g0014 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18956 | hp1 | a0001 | c0001 | t0043 | g0072 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18956 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18960 | hp1 | a0004 | c0003 | t0003 | g0164 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18962 | hp2 | a0001 | c0001 | t0010 | g0042 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18963 | hp2 | a0001 | c0001 | t0045 | g0080 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0111 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18965 | hp1 | a0004 | c0003 | t0006 | g0014 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18965 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18967 | hp2 | a0001 | c0001 | t0050 | g0088 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18980 | hp1 | a0004 | c0003 | t0006 | g0014 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18980 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18988 | hp2 | a0001 | c0001 | t0011 | g0090 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18989 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18989 | hp2 | a0001 | c0001 | t0011 | g0097 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18990 | hp1 | a0002 | c0002 | t0004 | g0151 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19001 | hp2 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19006 | hp2 | a0002 | c0002 | t0004 | g0153 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19010 | hp1 | a0001 | c0001 | t0033 | g0106 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19043 | hp2 | a0002 | c0002 | t0027 | g0145 | AFR | LWK | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19054 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19060 | hp1 | a0001 | c0001 | t0036 | g0162 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19062 | hp1 | a0001 | c0001 | t0016 | g0089 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19072 | hp1 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19075 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19076 | hp1 | a0001 | c0001 | t0009 | g0038 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19076 | hp2 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19085 | hp2 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19086 | hp1 | a0001 | c0001 | t0015 | g0011 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19087 | hp1 | a0001 | c0001 | t0031 | g0105 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19088 | hp1 | a0001 | c0001 | t0015 | g0011 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0011 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0026 | AFR | ASW | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0133 | AFR | ASW | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01123 | hp1 | a0002 | c0002 | t0018 | g0150 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02109 | hp1 | a0002 | c0002 | t0013 | g0016 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02109 | hp2 | a0002 | c0002 | t0007 | g0015 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02486 | hp1 | a0002 | c0002 | t0007 | g0015 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG03471 | hp2 | a0002 | c0002 | t0013 | g0016 | AFR | MSL | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG06807 | hp1 | a0002 | c0002 | t0026 | g0143 | AFR | USA | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0127 | REF | REF | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
homoSapiens | grch38p0 | a0003 | c0004 | t0002 | g0047 | REF | REF | MYEF2_chr15_48129632_48183295 | MYEF2 | chr15 | 48129632 | 48183295 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48149357 | T | C | 2 | a0002 a0006 |
33 | HG00544.hp2 HG01123.hp1 HG01167.hp1 others(30): Show |
missense_variant | MODERATE | c.1393A>G | p.Ser465Gly | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 15/17 | 1451/10137 | 1393/1803 | 465/600 | chr15 | 48149357 | |||
chr15:48153798 | G | A | 1 | a0004 | 5 | NA18952.hp1 NA18953.hp2 NA18960.hp1 others(2): Show |
missense_variant | MODERATE | c.1081C>T | p.Pro361Ser | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/17 | 1139/10137 | 1081/1803 | 361/600 | chr15 | 48153798 | |||
chr15:48159777 | C | A | 1 | a0005 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.553G>T | p.Ala185Ser | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 6/17 | 611/10137 | 553/1803 | 185/600 | chr15 | 48159777 | |||
chr15:48168730 | C | T | 5 | a0001 a0002 a0004 others(2): Show |
259 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(256): Show |
missense_variant | MODERATE | c.271G>A | p.Ala91Thr | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 2/17 | 329/10137 | 271/1803 | 91/600 | chr15 | 48168730 | |||
chr15:48168819 | T | C | 1 | a0006 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.182A>G | p.Lys61Arg | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 2/17 | 240/10137 | 182/1803 | 61/600 | chr15 | 48168819 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48158785 | T | C | 1 | a0002c0006 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.855A>G | p.Glu285Glu | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 7/17 | 913/10137 | 855/1803 | 285/600 | chr15 | 48158785 | |||
chr15:48178151 | C | G | 1 | a0005c0005 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.87G>C | p.Pro29Pro | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/17 | 145/10137 | 87/1803 | 29/600 | chr15 | 48178151 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48134635 | G | A | 1 | a0002c0006t0021 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8273C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 8273 | chr15 | 48134635 | ||||||
chr15:48135667 | G | A | 1 | a0001c0001t0041 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7241C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 7241 | chr15 | 48135667 | ||||||
chr15:48135710 | G | GA | 6 | a0001c0001t0008 a0001c0001t0020 a0001c0001t0035 others(3): Show |
10 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7197dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 7197 | chr15 | 48135710 | ||||||
chr15:48135710 | GA | G | 14 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(11): Show |
86 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*7197delT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 7197 | chr15 | 48135710 | ||||||
chr15:48135710 | GAA | G | 7 | a0001c0001t0019 a0002c0002t0004 a0002c0002t0013 others(4): Show |
24 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7196_*7197delTT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 7196 | chr15 | 48135710 | ||||||
chr15:48135762 | C | T | 2 | a0001c0001t0022 a0001c0001t0031 |
2 | HG03831.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7146G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 7146 | chr15 | 48135762 | ||||||
chr15:48135842 | G | A | 1 | a0001c0001t0047 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7066C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 7066 | chr15 | 48135842 | ||||||
chr15:48135927 | C | T | 1 | a0002c0002t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6981G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 6981 | chr15 | 48135927 | ||||||
chr15:48136069 | T | C | 3 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0049 |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6839A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 6839 | chr15 | 48136069 | ||||||
chr15:48136461 | T | TA | 4 | a0001c0001t0006 a0001c0001t0043 a0001c0001t0048 others(1): Show |
14 | HG01884.hp1 HG01928.hp2 HG01978.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6446dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 6446 | chr15 | 48136461 | ||||||
chr15:48136867 | C | T | 1 | a0001c0001t0046 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6041G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 6041 | chr15 | 48136867 | ||||||
chr15:48137157 | G | T | 1 | a0002c0002t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5751C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 5751 | chr15 | 48137157 | ||||||
chr15:48137391 | T | C | 6 | a0001c0001t0008 a0001c0001t0020 a0001c0001t0022 others(3): Show |
10 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5517A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 5517 | chr15 | 48137391 | ||||||
chr15:48137400 | G | T | 9 | a0002c0002t0004 a0002c0002t0007 a0002c0002t0013 others(6): Show |
31 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5508C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 5508 | chr15 | 48137400 | ||||||
chr15:48137944 | A | T | 1 | a0002c0002t0026 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4964T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4964 | chr15 | 48137944 | ||||||
chr15:48137988 | A | T | 1 | a0001c0001t0012 | 3 | HG03017.hp2 NA18964.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4920T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4920 | chr15 | 48137988 | ||||||
chr15:48138226 | C | G | 15 | a0001c0001t0008 a0001c0001t0020 a0001c0001t0022 others(12): Show |
41 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4682G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4682 | chr15 | 48138226 | ||||||
chr15:48138313 | C | A | 8 | a0002c0002t0004 a0002c0002t0007 a0002c0002t0013 others(5): Show |
30 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4595G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4595 | chr15 | 48138313 | ||||||
chr15:48138324 | T | C | 1 | a0001c0001t0033 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4584A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4584 | chr15 | 48138324 | ||||||
chr15:48138556 | T | C | 1 | a0001c0001t0014 | 3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4352A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4352 | chr15 | 48138556 | ||||||
chr15:48138802 | T | C | 1 | a0001c0001t0028 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4106A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4106 | chr15 | 48138802 | ||||||
chr15:48138818 | A | G | 1 | a0001c0001t0045 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4090T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4090 | chr15 | 48138818 | ||||||
chr15:48138853 | A | C | 1 | a0001c0001t0044 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4055T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 4055 | chr15 | 48138853 | ||||||
chr15:48138928 | C | T | 1 | a0001c0001t0030 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3980G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 3980 | chr15 | 48138928 | ||||||
chr15:48139285 | T | C | 1 | a0001c0001t0017 | 2 | HG01167.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3623A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 3623 | chr15 | 48139285 | ||||||
chr15:48139447 | T | C | 9 | a0001c0001t0018 a0001c0001t0035 a0002c0002t0004 others(6): Show |
30 | HG00544.hp2 HG01123.hp1 HG01167.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3461A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 3461 | chr15 | 48139447 | ||||||
chr15:48139484 | C | T | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3424G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 3424 | chr15 | 48139484 | ||||||
chr15:48139521 | T | TA | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(16): Show |
103 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3386dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 3386 | chr15 | 48139521 | ||||||
chr15:48139787 | A | C | 2 | a0001c0001t0035 a0001c0001t0040 |
2 | HG02280.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3121T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 3121 | chr15 | 48139787 | ||||||
chr15:48140402 | G | A | 1 | a0002c0002t0029 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2506C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 2506 | chr15 | 48140402 | ||||||
chr15:48140439 | G | A | 1 | a0001c0001t0036 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2469C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 2469 | chr15 | 48140439 | ||||||
chr15:48141297 | A | G | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(45): Show |
208 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*1611T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1611 | chr15 | 48141297 | ||||||
chr15:48141345 | G | T | 1 | a0001c0001t0039 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1563C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1563 | chr15 | 48141345 | ||||||
chr15:48141534 | G | A | 1 | a0001c0001t0035 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1374C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1374 | chr15 | 48141534 | ||||||
chr15:48141542 | A | G | 1 | a0001c0001t0038 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1366 | chr15 | 48141542 | ||||||
chr15:48141566 | C | T | 1 | a0001c0001t0037 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1342G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1342 | chr15 | 48141566 | ||||||
chr15:48141567 | G | A | 1 | a0001c0001t0036 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1341 | chr15 | 48141567 | ||||||
chr15:48141593 | C | CA | 16 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(13): Show |
86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1314dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 1314 | chr15 | 48141593 | ||||||
chr15:48142115 | G | A | 1 | a0001c0001t0048 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*793C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 793 | chr15 | 48142115 | ||||||
chr15:48142336 | G | A | 1 | a0001c0001t0049 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*572C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 572 | chr15 | 48142336 | ||||||
chr15:48142397 | C | A | 2 | a0001c0001t0016 a0001c0001t0050 |
4 | HG01934.hp2 HG01975.hp2 NA18967.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*511G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 17/17 | 511 | chr15 | 48142397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48143309 | G | A | 1 | a0002c0002t0004g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1640-238C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48143309 | |||||||
chr15:48143659 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1640-588C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48143659 | |||||||
chr15:48143825 | A | G | 2 | a0001c0001t0005g0034 a0002c0006t0021g0053 |
3 | HG02257.hp1 HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1640-754T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48143825 | |||||||
chr15:48143907 | G | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0034 a0001c0001t0005g0044 others(8): Show |
15 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-836C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48143907 | |||||||
chr15:48144000 | A | G | 2 | a0001c0001t0003g0102 a0001c0001t0005g0043 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1640-929T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48144000 | |||||||
chr15:48144149 | C | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0044 a0001c0001t0005g0121 others(2): Show |
8 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1640-1078G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48144149 | |||||||
chr15:48144211 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1640-1140G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48144211 | |||||||
chr15:48144296 | G | C | 11 | a0001c0001t0005g0010 a0001c0001t0005g0034 a0001c0001t0005g0044 others(8): Show |
15 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1640-1225C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48144296 | |||||||
chr15:48144439 | T | C | 1 | a0001c0001t0042g0085 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1640-1368A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48144439 | |||||||
chr15:48144901 | T | A | 5 | a0002c0002t0007g0015 a0002c0002t0007g0033 a0002c0002t0007g0144 others(2): Show |
8 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1640-1830A>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48144901 | |||||||
chr15:48145017 | T | C | 1 | a0001c0001t0039g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1640-1946A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145017 | |||||||
chr15:48145095 | T | C | 1 | a0002c0002t0004g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1640-2024A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145095 | |||||||
chr15:48145143 | C | G | 34 | a0001c0001t0008g0032 a0001c0001t0008g0048 a0001c0001t0020g0049 others(31): Show |
43 | HG00544.hp2 HG01123.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1640-2072G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145143 | |||||||
chr15:48145280 | C | G | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640-2209G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145280 | |||||||
chr15:48145297 | C | A | 1 | a0001c0001t0008g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1640-2226G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145297 | |||||||
chr15:48145827 | A | T | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640-2756T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145827 | |||||||
chr15:48145919 | A | T | 24 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(21): Show |
31 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1640-2848T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48145919 | |||||||
chr15:48146072 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
150 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1639+2960G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146072 | |||||||
chr15:48146197 | C | A | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1639+2835G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146197 | |||||||
chr15:48146200 | T | C | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1639+2832A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146200 | |||||||
chr15:48146392 | T | C | 1 | a0001c0001t0008g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1639+2640A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146392 | |||||||
chr15:48146524 | T | C | 1 | a0002c0002t0027g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1639+2508A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146524 | |||||||
chr15:48146655 | C | T | 24 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(21): Show |
31 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1639+2377G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146655 | |||||||
chr15:48146720 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(26): Show |
40 | HG00408.hp2 HG00597.hp1 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.1639+2312T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48146720 | |||||||
chr15:48147083 | A | C | 2 | a0002c0002t0025g0141 a0002c0002t0029g0142 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1639+1949T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48147083 | |||||||
chr15:48147282 | C | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0044 a0001c0001t0005g0121 others(2): Show |
8 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+1750G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48147282 | |||||||
chr15:48147301 | A | G | 34 | a0001c0001t0008g0032 a0001c0001t0008g0048 a0001c0001t0020g0049 others(31): Show |
43 | HG00544.hp2 HG01123.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1639+1731T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48147301 | |||||||
chr15:48147626 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0009g0038 |
5 | HG00597.hp1 NA18945.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.1639+1406G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48147626 | |||||||
chr15:48147844 | A | T | 1 | a0001c0001t0035g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1639+1188T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48147844 | |||||||
chr15:48147998 | C | T | 1 | a0002c0002t0007g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1639+1034G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48147998 | |||||||
chr15:48148142 | A | T | 1 | a0001c0001t0017g0026 | 2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1639+890T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148142 | |||||||
chr15:48148275 | T | G | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1639+757A>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148275 | |||||||
chr15:48148450 | C | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0034 a0001c0001t0005g0044 others(8): Show |
15 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1639+582G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148450 | |||||||
chr15:48148647 | T | C | 1 | a0001c0001t0006g0163 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1639+385A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148647 | |||||||
chr15:48148683 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1639+349A>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148683 | |||||||
chr15:48148702 | A | G | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1639+330T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148702 | |||||||
chr15:48148760 | C | A | 1 | a0001c0001t0002g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1639+272G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148760 | |||||||
chr15:48148914 | A | C | 2 | a0001c0001t0008g0032 a0002c0006t0021g0053 |
3 | HG02451.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1639+118T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 16/16 | chr15 | 48148914 | |||||||
chr15:48149413 | G | A | 1 | a0003c0004t0008g0046 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1379-42C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48149413 | |||||||
chr15:48149589 | C | T | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1379-218G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48149589 | |||||||
chr15:48149676 | A | G | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1379-305T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48149676 | |||||||
chr15:48149751 | T | C | 1 | a0002c0002t0025g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1379-380A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48149751 | |||||||
chr15:48149791 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1379-420A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48149791 | |||||||
chr15:48150085 | T | C | 1 | a0001c0001t0002g0029 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1379-714A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48150085 | |||||||
chr15:48150264 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1378+836C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48150264 | |||||||
chr15:48150338 | G | C | 3 | a0002c0002t0007g0015 a0002c0002t0007g0033 a0002c0002t0007g0170 |
6 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378+762C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48150338 | |||||||
chr15:48150380 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1378+720A>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48150380 | |||||||
chr15:48150594 | A | G | 1 | a0001c0001t0002g0027 | 2 | HG02083.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1378+506T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 14/16 | chr15 | 48150594 | |||||||
chr15:48151246 | G | A | 1 | a0001c0001t0020g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1307-75C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 13/16 | chr15 | 48151246 | |||||||
chr15:48151291 | G | C | 2 | a0001c0001t0012g0062 a0001c0001t0012g0111 |
2 | NA18964.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1307-120C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 13/16 | chr15 | 48151291 | |||||||
chr15:48151343 | A | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0061 others(4): Show |
16 | HG00609.hp1 HG00673.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1306+130T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 13/16 | chr15 | 48151343 | |||||||
chr15:48151644 | T | C | 1 | a0002c0002t0004g0156 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1208-73A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 12/16 | chr15 | 48151644 | |||||||
chr15:48151651 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1208-80A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 12/16 | chr15 | 48151651 | |||||||
chr15:48152551 | T | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
150 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1088-267A>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48152551 | |||||||
chr15:48152753 | T | C | 2 | a0001c0001t0014g0131 a0001c0001t0014g0132 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1088-469A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48152753 | |||||||
chr15:48152848 | A | T | 2 | a0002c0002t0004g0153 a0002c0002t0004g0154 |
2 | HG00544.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1088-564T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48152848 | |||||||
chr15:48152892 | T | C | 25 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(22): Show |
32 | HG00544.hp2 HG01123.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1088-608A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48152892 | |||||||
chr15:48152930 | T | C | 1 | a0002c0002t0029g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1088-646A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48152930 | |||||||
chr15:48152993 | TTACCCTC others(44): Show |
T | 11 | a0001c0001t0005g0010 a0001c0001t0005g0034 a0001c0001t0005g0044 others(8): Show |
15 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1087+748_1088-710d others(53): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48152993 | |||||||
chr15:48153190 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
150 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1087+602T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48153190 | |||||||
chr15:48153316 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1087+476C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48153316 | |||||||
chr15:48153327 | A | C | 1 | a0001c0001t0010g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1087+465T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 10/16 | chr15 | 48153327 | |||||||
chr15:48154198 | AT | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0082 others(4): Show |
11 | HG00597.hp1 HG02071.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.986-306delA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48154198 | |||||||
chr15:48154440 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.986-547T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48154440 | |||||||
chr15:48154952 | G | T | 23 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(20): Show |
30 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.986-1059C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48154952 | |||||||
chr15:48155011 | A | C | 1 | a0002c0002t0024g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.986-1118T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155011 | |||||||
chr15:48155413 | C | G | 3 | a0001c0001t0035g0045 a0001c0001t0040g0059 a0002c0002t0025g0141 |
3 | HG02280.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.986-1520G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155413 | |||||||
chr15:48155429 | T | C | 1 | a0001c0001t0044g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.986-1536A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155429 | |||||||
chr15:48155690 | G | GA | 5 | a0001c0001t0001g0084 a0001c0001t0001g0135 a0001c0001t0003g0092 others(2): Show |
5 | HG02145.hp2 HG03486.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.986-1798dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155690 | |||||||
chr15:48155690 | GA | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(14): Show |
35 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.986-1798delT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155690 | |||||||
chr15:48155703 | A | C | 24 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(21): Show |
31 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.986-1810T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155703 | |||||||
chr15:48155739 | A | G | 3 | a0001c0001t0035g0045 a0001c0001t0040g0059 a0002c0002t0025g0141 |
3 | HG02280.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.986-1846T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155739 | |||||||
chr15:48155774 | AT | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
242 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.986-1882delA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155774 | |||||||
chr15:48155847 | T | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.986-1954A>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155847 | |||||||
chr15:48155851 | T | C | 1 | a0001c0001t0003g0006 | 5 | HG02717.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.986-1958A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48155851 | |||||||
chr15:48156036 | C | T | 2 | a0001c0001t0035g0045 a0001c0001t0040g0059 |
2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.985+1957G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48156036 | |||||||
chr15:48156105 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.985+1888T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48156105 | |||||||
chr15:48156132 | T | C | 2 | a0001c0001t0035g0045 a0001c0001t0040g0059 |
2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.985+1861A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48156132 | |||||||
chr15:48156489 | A | C | 1 | a0001c0001t0008g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.985+1504T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48156489 | |||||||
chr15:48156667 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 others(62): Show |
113 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.985+1326A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48156667 | |||||||
chr15:48156984 | T | C | 1 | a0001c0001t0037g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.985+1009A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48156984 | |||||||
chr15:48157112 | G | C | 1 | a0002c0002t0025g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.985+881C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48157112 | |||||||
chr15:48157146 | T | C | 1 | a0001c0001t0018g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.985+847A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48157146 | |||||||
chr15:48157233 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.985+760C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48157233 | |||||||
chr15:48157285 | C | T | 3 | a0002c0002t0004g0039 a0002c0002t0004g0151 a0002c0002t0004g0152 |
3 | HG02040.hp2 NA18948.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.985+708G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48157285 | |||||||
chr15:48157903 | G | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.985+90C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 9/16 | chr15 | 48157903 | |||||||
chr15:48158060 | A | G | 2 | a0001c0001t0008g0032 a0002c0006t0021g0053 |
3 | HG02451.hp1 HG03130.hp2 HG03579.hp1 |
splice_region_variant&intron_variant | LOW | c.922-4T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 8/16 | chr15 | 48158060 | |||||||
chr15:48158127 | T | C | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.921+48A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 8/16 | chr15 | 48158127 | |||||||
chr15:48158268 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.872-44A>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 7/16 | chr15 | 48158268 | |||||||
chr15:48158320 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
220 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.872-96A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 7/16 | chr15 | 48158320 | |||||||
chr15:48158603 | G | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
221 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.871+166C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 7/16 | chr15 | 48158603 | |||||||
chr15:48159203 | G | A | 1 | a0002c0002t0013g0016 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.718-281C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 6/16 | chr15 | 48159203 | |||||||
chr15:48159450 | A | G | 1 | a0001c0001t0020g0049 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.717+163T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 6/16 | chr15 | 48159450 | |||||||
chr15:48159465 | C | A | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.717+148G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 6/16 | chr15 | 48159465 | |||||||
chr15:48159828 | A | G | 1 | a0001c0001t0038g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.526-24T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48159828 | |||||||
chr15:48159843 | T | C | 1 | a0001c0001t0009g0128 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.526-39A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48159843 | |||||||
chr15:48160088 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.526-284T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160088 | |||||||
chr15:48160173 | G | T | 3 | a0001c0001t0014g0131 a0001c0001t0014g0132 a0001c0001t0014g0133 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526-369C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160173 | |||||||
chr15:48160486 | T | TACACACA others(1): Show |
13 | a0002c0002t0004g0013 a0002c0002t0004g0036 a0002c0002t0004g0039 others(10): Show |
15 | HG00544.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.526-690_526-683dup others(8): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACACACA others(3): Show |
6 | a0002c0002t0004g0155 a0002c0002t0007g0015 a0002c0002t0007g0170 others(3): Show |
9 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-692_526-683dup others(10): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACACACA others(5): Show |
1 | a0002c0002t0007g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.526-694_526-683dup others(12): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACACACA others(7): Show |
3 | a0002c0002t0007g0144 a0002c0002t0025g0141 a0002c0002t0026g0143 |
3 | HG03195.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.526-696_526-683dup others(14): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATAC | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
201 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.526-683_526-682ins others(6): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(1): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0056 a0001c0001t0001g0087 others(6): Show |
12 | HG00423.hp2 HG01167.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-683_526-682ins others(8): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(3): Show |
3 | a0001c0001t0005g0010 a0001c0001t0005g0044 a0001c0001t0005g0121 |
6 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-683_526-682ins others(10): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(5): Show |
3 | a0001c0001t0028g0120 a0001c0001t0035g0045 a0001c0001t0040g0059 |
3 | HG02280.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.526-683_526-682ins others(12): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(9): Show |
1 | a0001c0001t0008g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.526-683_526-682ins others(16): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(11): Show |
1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.526-683_526-682ins others(18): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(13): Show |
1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526-683_526-682ins others(20): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160486 | T | TACATACA others(19): Show |
1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.526-683_526-682ins others(26): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160486 | |||||||
chr15:48160490 | C | T | 1 | a0001c0001t0005g0122 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526-686G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160490 | |||||||
chr15:48160602 | G | T | 26 | a0001c0001t0008g0032 a0002c0002t0004g0013 a0002c0002t0004g0031 others(23): Show |
34 | HG00544.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.526-798C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160602 | |||||||
chr15:48160609 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.526-805G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160609 | |||||||
chr15:48160684 | G | GAAGT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
220 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.526-884_526-881dup others(4): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160684 | |||||||
chr15:48160876 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.526-1072T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160876 | |||||||
chr15:48160879 | GA | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
221 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.526-1076delT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160879 | |||||||
chr15:48160919 | G | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.526-1115C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48160919 | |||||||
chr15:48161132 | T | C | 2 | a0002c0002t0025g0141 a0002c0002t0029g0142 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.526-1328A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48161132 | |||||||
chr15:48161189 | A | G | 1 | a0002c0002t0027g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.526-1385T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48161189 | |||||||
chr15:48161439 | T | C | 2 | a0001c0001t0005g0044 a0001c0001t0005g0121 |
2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.526-1635A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48161439 | |||||||
chr15:48161617 | T | C | 2 | a0001c0001t0016g0089 a0001c0001t0050g0088 |
2 | NA18967.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.526-1813A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48161617 | |||||||
chr15:48161811 | G | T | 18 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(15): Show |
22 | HG00544.hp2 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.526-2007C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48161811 | |||||||
chr15:48162080 | T | A | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526-2276A>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48162080 | |||||||
chr15:48162632 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.526-2828C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48162632 | |||||||
chr15:48162662 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.526-2858G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48162662 | |||||||
chr15:48163064 | G | A | 1 | a0002c0002t0029g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.525+2869C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48163064 | |||||||
chr15:48163178 | A | C | 1 | a0001c0001t0003g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.525+2755T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48163178 | |||||||
chr15:48163431 | C | G | 1 | a0001c0001t0006g0159 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.525+2502G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48163431 | |||||||
chr15:48163706 | C | T | 1 | a0001c0001t0005g0034 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.525+2227G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48163706 | |||||||
chr15:48164211 | C | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0034 a0001c0001t0005g0044 others(8): Show |
15 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.525+1722G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48164211 | |||||||
chr15:48164223 | G | A | 1 | a0004c0003t0006g0166 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.525+1710C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48164223 | |||||||
chr15:48164657 | T | C | 2 | a0001c0001t0008g0048 a0001c0001t0020g0049 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.525+1276A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48164657 | |||||||
chr15:48164695 | C | G | 2 | a0001c0001t0006g0096 a0001c0001t0011g0097 |
2 | NA18989.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.525+1238G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48164695 | |||||||
chr15:48164814 | T | G | 1 | a0004c0003t0006g0166 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.525+1119A>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48164814 | |||||||
chr15:48164972 | C | G | 1 | a0001c0001t0005g0095 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.525+961G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48164972 | |||||||
chr15:48165061 | G | C | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.525+872C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48165061 | |||||||
chr15:48165136 | C | T | 1 | a0002c0002t0027g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.525+797G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48165136 | |||||||
chr15:48165533 | T | G | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.525+400A>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48165533 | |||||||
chr15:48165793 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0011g0090 |
5 | HG00609.hp1 NA18612.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+140A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48165793 | |||||||
chr15:48165795 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0157 |
2 | NA18612.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.525+138C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48165795 | |||||||
chr15:48165885 | C | T | 1 | a0001c0001t0012g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.525+48G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 5/16 | chr15 | 48165885 | |||||||
chr15:48166467 | T | C | 5 | a0002c0002t0007g0015 a0002c0002t0007g0033 a0002c0002t0007g0144 others(2): Show |
8 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-339A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 3/16 | chr15 | 48166467 | |||||||
chr15:48166783 | TAA | T | 5 | a0002c0002t0007g0015 a0002c0002t0007g0033 a0002c0002t0007g0144 others(2): Show |
8 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.423+564_423+565del others(2): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 3/16 | chr15 | 48166783 | |||||||
chr15:48166877 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.423+472C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 3/16 | chr15 | 48166877 | |||||||
chr15:48167040 | A | G | 1 | a0002c0002t0025g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.423+309T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 3/16 | chr15 | 48167040 | |||||||
chr15:48167313 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.423+36A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 3/16 | chr15 | 48167313 | |||||||
chr15:48167881 | A | G | 1 | a0001c0001t0002g0093 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.371-480T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 2/16 | chr15 | 48167881 | |||||||
chr15:48167938 | A | G | 1 | a0001c0001t0008g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.371-537T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 2/16 | chr15 | 48167938 | |||||||
chr15:48167991 | G | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 others(57): Show |
106 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.371-590C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 2/16 | chr15 | 48167991 | |||||||
chr15:48168589 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
222 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.370+42A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 2/16 | chr15 | 48168589 | |||||||
chr15:48168949 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 others(61): Show |
112 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.162-110A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48168949 | |||||||
chr15:48169178 | G | C | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.162-339C>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169178 | |||||||
chr15:48169182 | C | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
206 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.162-343G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169182 | |||||||
chr15:48169599 | A | AT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0040g0059 |
7 | HG01891.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-761dupA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169599 | |||||||
chr15:48169599 | AT | A | 93 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0029 others(90): Show |
152 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.162-761delA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169599 | |||||||
chr15:48169604 | T | C | 6 | a0001c0001t0005g0122 a0001c0001t0014g0131 a0001c0001t0014g0132 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-765A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169604 | |||||||
chr15:48169663 | T | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162-824A>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169663 | |||||||
chr15:48169787 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162-948C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169787 | |||||||
chr15:48169886 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.162-1047G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169886 | |||||||
chr15:48169898 | C | G | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162-1059G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48169898 | |||||||
chr15:48170110 | G | GT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0003g0064 others(2): Show |
6 | HG00423.hp2 HG00438.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-1272dupA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170110 | |||||||
chr15:48170123 | T | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0167 |
2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.162-1284A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170123 | |||||||
chr15:48170195 | G | T | 1 | a0002c0002t0004g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.162-1356C>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170195 | |||||||
chr15:48170360 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
259 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.162-1521A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170360 | |||||||
chr15:48170361 | G | A | 1 | a0001c0001t0035g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.162-1522C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170361 | |||||||
chr15:48170714 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0006g0168 a0001c0001t0009g0128 |
5 | NA18944.hp2 NA18963.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-1875A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170714 | |||||||
chr15:48170828 | A | G | 2 | a0001c0001t0035g0045 a0001c0001t0040g0059 |
2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.162-1989T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170828 | |||||||
chr15:48170921 | A | T | 1 | a0002c0002t0007g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.162-2082T>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48170921 | |||||||
chr15:48171510 | AT | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
254 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.162-2672delA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48171510 | |||||||
chr15:48171713 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
222 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.162-2874T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48171713 | |||||||
chr15:48171943 | T | C | 17 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(14): Show |
21 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.162-3104A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48171943 | |||||||
chr15:48172086 | G | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
251 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.162-3247C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48172086 | |||||||
chr15:48172169 | G | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162-3330C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48172169 | |||||||
chr15:48172400 | C | CA | 5 | a0002c0002t0007g0015 a0002c0002t0007g0033 a0002c0002t0007g0144 others(2): Show |
8 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-3562dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48172400 | |||||||
chr15:48172531 | T | C | 25 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(22): Show |
32 | HG00544.hp2 HG01123.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-3692A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48172531 | |||||||
chr15:48173140 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.162-4301G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48173140 | |||||||
chr15:48173250 | G | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162-4411C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48173250 | |||||||
chr15:48173278 | T | C | 18 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(15): Show |
22 | HG00544.hp2 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.162-4439A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48173278 | |||||||
chr15:48173437 | A | G | 1 | a0001c0001t0012g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.162-4598T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48173437 | |||||||
chr15:48173980 | A | G | 1 | a0002c0002t0004g0050 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.161+4097T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48173980 | |||||||
chr15:48174012 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.161+4065T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48174012 | |||||||
chr15:48174391 | AT | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
245 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.161+3685delA | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48174391 | |||||||
chr15:48174391 | ATT | A | 4 | a0001c0001t0039g0130 a0002c0002t0004g0013 a0002c0002t0004g0051 others(1): Show |
6 | HG01243.hp2 HG01257.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+3684_161+3685d others(4): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48174391 | |||||||
chr15:48174407 | A | C | 1 | a0001c0001t0002g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.161+3670T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48174407 | |||||||
chr15:48174812 | G | A | 1 | a0001c0001t0022g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.161+3265C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48174812 | |||||||
chr15:48174959 | T | C | 3 | a0001c0001t0014g0131 a0001c0001t0014g0132 a0001c0001t0014g0133 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.161+3118A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48174959 | |||||||
chr15:48175147 | A | C | 1 | a0001c0001t0002g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161+2930T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175147 | |||||||
chr15:48175190 | T | C | 1 | a0002c0006t0021g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.161+2887A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175190 | |||||||
chr15:48175224 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.161+2853G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175224 | |||||||
chr15:48175286 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.161+2791C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175286 | |||||||
chr15:48175446 | A | C | 2 | a0001c0001t0019g0018 a0001c0001t0037g0055 |
3 | HG02615.hp1 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.161+2631T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175446 | |||||||
chr15:48175504 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.161+2573G>A | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175504 | |||||||
chr15:48175822 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
220 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.161+2255A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48175822 | |||||||
chr15:48176219 | T | TA | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0030 others(6): Show |
10 | HG00597.hp2 HG01123.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+1857dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176219 | |||||||
chr15:48176219 | T | TAA | 13 | a0001c0001t0001g0149 a0002c0002t0004g0146 a0002c0002t0007g0015 others(10): Show |
17 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+1856_161+1857d others(4): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176219 | |||||||
chr15:48176219 | T | TAAA | 11 | a0002c0002t0004g0013 a0002c0002t0004g0031 a0002c0002t0004g0036 others(8): Show |
14 | HG00544.hp2 HG01123.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+1855_161+1857d others(5): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176219 | |||||||
chr15:48176219 | TA | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0005g0043 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1857delT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176219 | |||||||
chr15:48176311 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.161+1766C>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176311 | |||||||
chr15:48176339 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.161+1738A>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176339 | |||||||
chr15:48176364 | A | G | 1 | a0002c0002t0004g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.161+1713T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176364 | |||||||
chr15:48176933 | AAG | A | 1 | a0001c0001t0008g0032 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.161+1142_161+1143d others(4): Show |
MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48176933 | |||||||
chr15:48177118 | A | C | 1 | a0002c0002t0013g0016 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+959T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48177118 | |||||||
chr15:48177394 | T | TA | 15 | a0001c0001t0002g0167 a0001c0001t0003g0160 a0001c0001t0006g0159 others(12): Show |
20 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.161+682dupT | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48177394 | |||||||
chr15:48177506 | A | G | 1 | a0001c0001t0009g0038 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.161+571T>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48177506 | |||||||
chr15:48177727 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.161+350T>G | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48177727 | |||||||
chr15:48177745 | C | A | 1 | a0001c0001t0005g0034 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.161+332G>T | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48177745 | |||||||
chr15:48178042 | C | G | 1 | a0002c0002t0004g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.161+35G>C | MYEF2 | ENSG00000104177.20 | transcript | ENST00000324324.12 | protein_coding | 1/16 | chr15 | 48178042 |