Item | Value |
---|---|
geneid | 57707 |
ensemblid | ENSG00000140950.16 |
hgncid | 29325 |
symbol | MEAK7 |
name | MTOR associated protein, eak-7 homolog |
refseq_nuc | NM_020947.4 |
refseq_prot | NP_065998.3 |
ensembl_nuc | ENST00000343629.11 |
ensembl_prot | ENSP00000343635.6 |
mane_status | MANE Select |
chr | chr16 |
start | 84476355 |
end | 84504659 |
strand | - |
ver | v1.2 |
region | chr16:84476355-84504659 |
region5000 | chr16:84471355-84509659 |
regionname0 | MEAK7_chr16_84476355_84504659 |
regionname5000 | MEAK7_chr16_84471355_84509659 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 456 | 315 | 30 | 52 | 187 | 9 | 37 | 144 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0002 | 0/0 | 456 | 93 | 30 | 19 | 28 | 6 | 10 | 23 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0003 | 0/0 | 456 | 18 | 15 | 3 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0004 | 0/0 | 456 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0005 | 1/0 | 456 | 6 | 4 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0006 | 0/0 | 456 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0007 | 0/0 | 456 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0008 | 0/0 | 456 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0009 | 0/0 | 456 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0010 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0011 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0012 | 0/0 | 456 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0013 | 0/0 | 456 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0014 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0015 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0016 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0017 | 0/0 | 456 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0018 | 0/0 | 456 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0019 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0020 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0021 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0022 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
a0023 | 0/1 | 456 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | MGNSR others(451): Show |
chr16 | 84471355 | 84509659 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1368 | 198 | 17 | 45 | 106 | 3 | 27 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0001c0002 | 0/0 | 1368 | 90 | 2 | 6 | 69 | 3 | 10 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0001c0005 | 0/0 | 1368 | 15 | 4 | 0 | 9 | 2 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0001c0006 | 0/0 | 1368 | 7 | 7 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0001c0017 | 0/0 | 1368 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0001c0018 | 0/0 | 1368 | 2 | 0 | 1 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0001c0027 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0003 | 0/0 | 1368 | 70 | 12 | 16 | 26 | 6 | 10 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0009 | 0/0 | 1368 | 6 | 5 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0010 | 0/0 | 1368 | 5 | 5 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0013 | 0/0 | 1368 | 4 | 4 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0015 | 0/0 | 1368 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0016 | 0/0 | 1368 | 2 | 1 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0019 | 0/0 | 1368 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0023 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0002c0035 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0003c0004 | 0/0 | 1368 | 18 | 15 | 3 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0004c0011 | 0/0 | 1368 | 5 | 5 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0004c0020 | 0/0 | 1368 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0005c0008 | 1/0 | 1368 | 6 | 4 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0006c0007 | 0/0 | 1368 | 6 | 0 | 1 | 5 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0007c0012 | 0/0 | 1368 | 4 | 4 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0008c0014 | 0/0 | 1368 | 3 | 0 | 3 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0009c0036 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0009c0037 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0010c0022 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0011c0024 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0012c0032 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0013c0033 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0014c0025 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0015c0038 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0016c0034 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0017c0021 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0018c0029 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0019c0030 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0020c0028 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0021c0031 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0022c0039 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 | ||
a0023c0026 | 0/1 | 1368 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | ATGGG others(1363): Show |
chr16 | 84471355 | 84509659 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4957 | 10 | 0 | 0 | 10 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0002 | 0/0 | 4938 | 7 | 0 | 0 | 7 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0003 | 0/0 | 4977 | 12 | 0 | 0 | 10 | 0 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0004 | 0/0 | 4976 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0005 | 0/0 | 4958 | 13 | 0 | 9 | 1 | 0 | 3 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4953): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0006 | 0/0 | 4995 | 4 | 0 | 2 | 1 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0008 | 0/0 | 5052 | 6 | 0 | 0 | 6 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5047): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0009 | 0/0 | 4996 | 8 | 0 | 3 | 1 | 1 | 3 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0011 | 0/0 | 4958 | 7 | 0 | 5 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4953): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0012 | 0/0 | 4919 | 2 | 0 | 1 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0013 | 0/0 | 5015 | 6 | 0 | 3 | 0 | 1 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0016 | 0/0 | 4920 | 4 | 0 | 0 | 3 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4915): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0017 | 0/0 | 4976 | 5 | 0 | 0 | 4 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0021 | 0/0 | 4957 | 4 | 0 | 0 | 4 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0022 | 0/0 | 4976 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0023 | 0/0 | 5015 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0024 | 0/0 | 4976 | 2 | 1 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0030 | 0/0 | 4977 | 3 | 3 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0031 | 0/0 | 4938 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0033 | 0/0 | 4995 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0035 | 0/0 | 4940 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4935): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0036 | 0/0 | 4957 | 2 | 0 | 1 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0039 | 0/0 | 5015 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0045 | 0/0 | 4939 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0046 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0053 | 0/0 | 4977 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0054 | 0/0 | 4900 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4895): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0055 | 0/0 | 4919 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0057 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0058 | 0/0 | 4939 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0059 | 0/0 | 4939 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0060 | 0/0 | 5259 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5254): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0065 | 0/0 | 4995 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0067 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5330): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0068 | 0/0 | 5034 | 2 | 0 | 0 | 0 | 0 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5029): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0070 | 0/0 | 4977 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0074 | 0/0 | 4919 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0075 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0077 | 0/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0086 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0087 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5028): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0089 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5085): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0091 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0100 | 0/0 | 5053 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5048): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0101 | 0/0 | 5091 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5086): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0102 | 0/0 | 5411 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5406): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0103 | 0/0 | 5110 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5105): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0104 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5430): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0105 | 0/0 | 5243 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5238): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0119 | 0/0 | 4919 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0125 | 0/0 | 5015 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0131 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0134 | 0/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0144 | 0/0 | 5185 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5180): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0147 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0150 | 0/0 | 5204 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5199): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0154 | 0/0 | 4901 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4896): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0155 | 0/0 | 5232 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5227): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0156 | 0/0 | 5231 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5226): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0157 | 0/0 | 5230 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5225): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0158 | 0/0 | 5223 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5218): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0159 | 0/0 | 5222 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5217): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0160 | 0/0 | 5221 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5216): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0161 | 0/0 | 5223 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5218): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0164 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4915): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0166 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5237): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0168 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0170 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0172 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0173 | 0/0 | 5262 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5257): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0174 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5256): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0178 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0180 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4953): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0182 | 0/0 | 5278 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5273): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0184 | 0/0 | 4996 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0185 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0186 | 0/0 | 4978 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4973): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0191 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5302): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0192 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5298): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0194 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0197 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0198 | 0/0 | 5318 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5313): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0199 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0201 | 0/0 | 5326 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5321): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0202 | 0/0 | 5325 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5320): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0203 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5315): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0204 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0206 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5028): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0208 | 0/0 | 5053 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5048): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0209 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5047): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0211 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5047): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0213 | 0/0 | 5450 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5445): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0215 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0216 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0217 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0220 | 0/0 | 4919 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0221 | 0/0 | 4996 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0223 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0228 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5047): Show |
chr16 | 84471355 | 84509659 |
a0001c0001t0229 | 0/0 | 5015 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0001 | 0/0 | 4957 | 19 | 0 | 1 | 16 | 2 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0002 | 0/0 | 4938 | 9 | 0 | 1 | 8 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0003 | 0/0 | 4977 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0004 | 0/0 | 4976 | 11 | 0 | 1 | 10 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0006 | 0/0 | 4995 | 7 | 0 | 0 | 4 | 1 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0012 | 0/0 | 4919 | 4 | 0 | 1 | 2 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0022 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0023 | 0/0 | 5015 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0026 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5028): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0034 | 0/0 | 5014 | 3 | 1 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0038 | 0/0 | 4995 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0056 | 0/0 | 4938 | 2 | 0 | 0 | 0 | 0 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0059 | 0/0 | 4939 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0061 | 0/0 | 4957 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0063 | 0/0 | 4976 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0066 | 0/0 | 4995 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0081 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0082 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0083 | 0/0 | 5014 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0110 | 0/0 | 5300 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5295): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0143 | 0/0 | 5300 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5295): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0146 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0148 | 0/0 | 5014 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0151 | 0/0 | 4901 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4896): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0152 | 0/0 | 4900 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4895): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0153 | 0/0 | 4900 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4895): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0165 | 0/0 | 4919 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0169 | 0/0 | 4939 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0171 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0176 | 0/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0177 | 0/0 | 4957 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0181 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5281): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0188 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0189 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0190 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0195 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0200 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4989): Show |
chr16 | 84471355 | 84509659 |
a0001c0002t0214 | 0/0 | 5223 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5218): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0003 | 0/0 | 4977 | 4 | 0 | 0 | 4 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0064 | 0/0 | 4977 | 2 | 0 | 0 | 1 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0071 | 0/0 | 4977 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0072 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4876): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0073 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0129 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5027): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0130 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5329): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0140 | 0/0 | 4977 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0141 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0149 | 0/0 | 4882 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4877): Show |
chr16 | 84471355 | 84509659 |
a0001c0005t0179 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0006t0043 | 0/0 | 4937 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4932): Show |
chr16 | 84471355 | 84509659 |
a0001c0006t0044 | 0/0 | 4957 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0006t0069 | 0/0 | 4957 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0006t0113 | 0/0 | 4958 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4953): Show |
chr16 | 84471355 | 84509659 |
a0001c0006t0137 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0001c0017t0022 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0017t0175 | 0/0 | 5260 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5255): Show |
chr16 | 84471355 | 84509659 |
a0001c0018t0024 | 0/0 | 4976 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0001c0018t0078 | 0/0 | 4957 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0001c0027t0029 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0001 | 0/0 | 4957 | 2 | 0 | 1 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0006 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0007 | 0/0 | 4976 | 11 | 0 | 2 | 9 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0010 | 0/0 | 4957 | 5 | 0 | 2 | 1 | 1 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0014 | 0/0 | 5014 | 4 | 0 | 0 | 4 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0015 | 0/0 | 4957 | 5 | 0 | 0 | 5 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0019 | 0/0 | 4995 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0028 | 0/0 | 5091 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5086): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0029 | 0/0 | 4976 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0032 | 0/0 | 4957 | 3 | 0 | 1 | 0 | 2 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0042 | 0/0 | 5110 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5105): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0047 | 0/0 | 4976 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0048 | 0/0 | 4995 | 2 | 0 | 0 | 0 | 0 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0049 | 0/0 | 5033 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5028): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0050 | 0/0 | 4957 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0062 | 0/0 | 4976 | 2 | 0 | 1 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0067 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5330): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0093 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4951): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0112 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4876): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0115 | 0/0 | 4937 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4932): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0116 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0117 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4876): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0118 | 0/0 | 4900 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4895): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0120 | 0/0 | 5241 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5236): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0122 | 0/0 | 4956 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4951): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0123 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0124 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0126 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0127 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5066): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0128 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5256): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0135 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4951): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0136 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4951): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0139 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4932): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0145 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4856): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0162 | 0/0 | 4919 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4914): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0207 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5028): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0210 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5369): Show |
chr16 | 84471355 | 84509659 |
a0002c0003t0212 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5369): Show |
chr16 | 84471355 | 84509659 |
a0002c0009t0020 | 0/0 | 4976 | 4 | 4 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0009t0218 | 0/0 | 4976 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0009t0227 | 0/0 | 4976 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0002c0010t0040 | 0/0 | 5148 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5143): Show |
chr16 | 84471355 | 84509659 |
a0002c0010t0044 | 0/0 | 4957 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0002c0010t0132 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0002c0010t0133 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0002c0013t0025 | 0/0 | 5015 | 3 | 3 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0002c0013t0085 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5010): Show |
chr16 | 84471355 | 84509659 |
a0002c0015t0183 | 0/0 | 5282 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5277): Show |
chr16 | 84471355 | 84509659 |
a0002c0015t0193 | 0/0 | 5301 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5296): Show |
chr16 | 84471355 | 84509659 |
a0002c0016t0051 | 0/0 | 4939 | 2 | 1 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0002c0019t0027 | 0/0 | 4996 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0002c0023t0196 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0002c0035t0027 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0018 | 0/0 | 5053 | 4 | 3 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5048): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0028 | 0/0 | 5091 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5086): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0041 | 0/0 | 4977 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0042 | 0/0 | 5110 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5105): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0052 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5103): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0107 | 0/0 | 5091 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5086): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0108 | 0/0 | 5410 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5405): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0138 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5103): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0163 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4916): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0187 | 0/0 | 4978 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4973): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0222 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0225 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5029): Show |
chr16 | 84471355 | 84509659 |
a0003c0004t0226 | 0/0 | 5053 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5048): Show |
chr16 | 84471355 | 84509659 |
a0004c0011t0092 | 0/0 | 4958 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4953): Show |
chr16 | 84471355 | 84509659 |
a0004c0011t0094 | 0/0 | 5053 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5048): Show |
chr16 | 84471355 | 84509659 |
a0004c0011t0095 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5067): Show |
chr16 | 84471355 | 84509659 |
a0004c0011t0096 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5124): Show |
chr16 | 84471355 | 84509659 |
a0004c0011t0097 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5162): Show |
chr16 | 84471355 | 84509659 |
a0004c0020t0121 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4934): Show |
chr16 | 84471355 | 84509659 |
a0004c0020t0142 | 0/0 | 5204 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5199): Show |
chr16 | 84471355 | 84509659 |
a0005c0008t0079 | 0/0 | 4977 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0005c0008t0080 | 0/0 | 4977 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0005c0008t0088 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5067): Show |
chr16 | 84471355 | 84509659 |
a0005c0008t0090 | 0/0 | 4977 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4972): Show |
chr16 | 84471355 | 84509659 |
a0005c0008t0098 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0005c0008t0111 | 1/0 | 5013 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5008): Show |
chr16 | 84471355 | 84509659 |
a0006c0007t0006 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0006c0007t0008 | 0/0 | 5052 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5047): Show |
chr16 | 84471355 | 84509659 |
a0006c0007t0026 | 0/0 | 5033 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5028): Show |
chr16 | 84471355 | 84509659 |
a0007c0012t0037 | 0/0 | 4976 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0007c0012t0076 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0007c0012t0084 | 0/0 | 5013 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5008): Show |
chr16 | 84471355 | 84509659 |
a0008c0014t0010 | 0/0 | 4957 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0008c0014t0046 | 0/0 | 4938 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0009c0036t0099 | 0/0 | 4937 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4932): Show |
chr16 | 84471355 | 84509659 |
a0009c0037t0114 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4970): Show |
chr16 | 84471355 | 84509659 |
a0010c0022t0057 | 0/0 | 4938 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0011c0024t0004 | 0/0 | 4976 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0012c0032t0019 | 0/0 | 4995 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4990): Show |
chr16 | 84471355 | 84509659 |
a0013c0033t0106 | 0/0 | 4996 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0014c0025t0224 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4991): Show |
chr16 | 84471355 | 84509659 |
a0015c0038t0052 | 0/0 | 5108 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5103): Show |
chr16 | 84471355 | 84509659 |
a0016c0034t0167 | 0/0 | 5241 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5236): Show |
chr16 | 84471355 | 84509659 |
a0017c0021t0007 | 0/0 | 4976 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4971): Show |
chr16 | 84471355 | 84509659 |
a0018c0029t0205 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0019c0030t0109 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4952): Show |
chr16 | 84471355 | 84509659 |
a0020c0028t0002 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4933): Show |
chr16 | 84471355 | 84509659 |
a0021c0031t0219 | 0/0 | 4901 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4896): Show |
chr16 | 84471355 | 84509659 |
a0022c0039t0014 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(5009): Show |
chr16 | 84471355 | 84509659 |
a0023c0026t0016 | 0/1 | 4920 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | CTCGA others(4915): Show |
chr16 | 84471355 | 84509659 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0005g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0006g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0008g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0008g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0008g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0008g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0008g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0011g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0012g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0012g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0013g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0013g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0013g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0013g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0016g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0016g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0016g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0016g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0017g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0017g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0017g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0021g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0021g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0021g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0021g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0022g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0022g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0023g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0023g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0024g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0024g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0030g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0030g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0030g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0031g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0033g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0033g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0033g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0035g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0035g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0036g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0036g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0039g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0045g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0046g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0053g0434 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0053g0435 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0054g0415 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0054g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0055g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0055g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0057g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0058g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0058g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0059g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0060g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0060g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0065g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0065g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0067g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0068g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0068g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0070g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0074g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0075g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0077g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0086g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0087g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0089g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0091g0430 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0100g0429 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0101g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0102g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0103g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0104g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0105g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0119g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0125g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0131g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0134g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0144g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0147g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0150g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0154g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0155g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0156g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0157g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0158g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0159g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0160g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0161g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0164g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0166g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0168g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0170g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0172g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0173g0420 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0174g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0178g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0180g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0182g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0184g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0185g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0186g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0191g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0192g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0194g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0197g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0198g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0199g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0201g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0202g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0203g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0204g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0206g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0208g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0209g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0211g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0213g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0215g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0216g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0217g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0220g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0221g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0223g0441 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0228g0443 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0001t0229g0449 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0001g0440 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0002g0439 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0003g0406 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0004g0404 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0006g0417 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0012g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0012g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0012g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0012g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0022g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0023g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0026g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0034g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0034g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0034g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0038g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0038g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0056g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0056g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0059g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0061g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0061g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0063g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0063g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0066g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0066g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0081g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0082g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0083g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0110g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0143g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0146g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0148g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0151g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0152g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0153g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0165g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0169g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0171g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0176g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0177g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0181g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0188g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0189g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0190g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0195g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0200g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0002t0214g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0064g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0064g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0071g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0072g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0073g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0129g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0130g0431 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0140g0432 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0141g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0149g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0005t0179g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0043g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0043g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0044g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0069g0445 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0069g0446 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0113g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0006t0137g0421 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0017t0022g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0017t0175g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0018t0024g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0018t0078g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0001c0027t0029g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0007g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0010g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0010g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0010g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0014g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0014g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0015g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0015g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0015g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0019g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0019g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0028g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0029g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0029g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0032g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0032g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0042g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0047g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0047g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0048g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0049g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0050g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0062g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0062g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0067g0426 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0093g0437 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0112g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0115g0438 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0116g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0117g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0118g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0120g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0122g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0123g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0124g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0126g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0127g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0128g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0135g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0136g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0139g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0145g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0162g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0207g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0210g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0003t0212g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0009t0020g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0009t0020g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0009t0020g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0009t0020g0425 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0009t0218g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0009t0227g0444 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0010t0040g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0010t0044g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0010t0132g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0010t0133g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0013t0025g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0013t0025g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0013t0025g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0013t0085g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0015t0183g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0015t0193g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0016t0051g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0016t0051g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0019t0027g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0019t0027g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0023t0196g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0002c0035t0027g0433 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0018g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0018g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0018g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0018g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0028g0422 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0028g0424 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0041g0427 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0041g0428 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0042g0423 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0052g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0107g0436 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0108g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0138g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0163g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0187g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0222g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0225g0448 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0003c0004t0226g0442 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0011t0092g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0011t0094g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0011t0095g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0011t0096g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0011t0097g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0020t0121g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0004c0020t0142g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0005c0008t0079g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0005c0008t0080g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0005c0008t0088g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0005c0008t0090g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0005c0008t0098g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0005c0008t0111g0419 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0006c0007t0006g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0006c0007t0008g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0006c0007t0008g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0006c0007t0026g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0006c0007t0026g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0007c0012t0037g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0007c0012t0037g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0007c0012t0076g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0007c0012t0084g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0008c0014t0010g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0008c0014t0046g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0009c0036t0099g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0009c0037t0114g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0010c0022t0057g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0011c0024t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0012c0032t0019g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0013c0033t0106g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0014c0025t0224g0447 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0015c0038t0052g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0016c0034t0167g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0017c0021t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0018c0029t0205g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0019c0030t0109g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0020c0028t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0021c0031t0219g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0022c0039t0014g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
a0023c0026t0016g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0010 | c0022 | t0057 | g0182 | EUR | GBR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00099 | hp2 | a0001 | c0001 | t0009 | g0252 | EUR | GBR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00140 | hp1 | a0001 | c0002 | t0006 | g0417 | EUR | GBR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00140 | hp2 | a0011 | c0024 | t0004 | g0185 | EUR | GBR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00280 | hp1 | a0001 | c0018 | t0024 | g0208 | EUR | FIN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0285 | EUR | FIN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00323 | hp1 | a0001 | c0001 | t0013 | g0144 | EUR | FIN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00323 | hp2 | a0001 | c0005 | t0064 | g0039 | EUR | FIN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00423 | hp1 | a0001 | c0005 | t0149 | g0294 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00423 | hp2 | a0002 | c0003 | t0019 | g0147 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00438 | hp1 | a0001 | c0002 | t0189 | g0284 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00438 | hp2 | a0001 | c0017 | t0175 | g0183 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00544 | hp2 | a0001 | c0001 | t0174 | g0399 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0241 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00597 | hp1 | a0001 | c0001 | t0021 | g0163 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00597 | hp2 | a0001 | c0001 | t0017 | g0174 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00609 | hp1 | a0001 | c0002 | t0110 | g0276 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0440 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00621 | hp1 | a0001 | c0001 | t0203 | g0220 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00639 | hp1 | a0002 | c0016 | t0051 | g0217 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00639 | hp2 | a0001 | c0001 | t0087 | g0212 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00673 | hp1 | a0002 | c0003 | t0007 | g0138 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | CHS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00733 | hp1 | a0002 | c0023 | t0196 | g0209 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00733 | hp2 | a0012 | c0032 | t0019 | g0036 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00735 | hp1 | a0003 | c0004 | t0163 | g0324 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00735 | hp2 | a0001 | c0001 | t0011 | g0227 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00738 | hp1 | a0001 | c0001 | t0009 | g0250 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00738 | hp2 | a0001 | c0001 | t0013 | g0218 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0213 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0349 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0065 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01069 | hp2 | a0002 | c0003 | t0049 | g0005 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01070 | hp1 | a0008 | c0014 | t0010 | g0014 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01070 | hp2 | a0001 | c0001 | t0036 | g0136 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01071 | hp1 | a0002 | c0003 | t0049 | g0005 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01071 | hp2 | a0008 | c0014 | t0010 | g0014 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01081 | hp1 | a0002 | c0003 | t0050 | g0009 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01081 | hp2 | a0002 | c0003 | t0006 | g0131 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01099 | hp1 | a0001 | c0001 | t0160 | g0269 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0154 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01106 | hp1 | a0002 | c0003 | t0050 | g0009 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01106 | hp2 | a0001 | c0001 | t0086 | g0214 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01109 | hp1 | a0002 | c0003 | t0116 | g0126 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01109 | hp2 | a0001 | c0001 | t0105 | g0186 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01168 | hp1 | a0001 | c0001 | t0013 | g0254 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01168 | hp2 | a0002 | c0003 | t0032 | g0008 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01169 | hp1 | a0001 | c0001 | t0013 | g0255 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01169 | hp2 | a0002 | c0003 | t0115 | g0438 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01175 | hp1 | a0001 | c0001 | t0067 | g0394 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01175 | hp2 | a0002 | c0009 | t0218 | g0384 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0249 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01192 | hp2 | a0001 | c0001 | t0074 | g0145 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01243 | hp1 | a0001 | c0001 | t0100 | g0429 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01243 | hp2 | a0001 | c0001 | t0220 | g0387 | AMR | PUR | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01255 | hp1 | a0013 | c0033 | t0106 | g0373 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01255 | hp2 | a0002 | c0003 | t0062 | g0378 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01256 | hp1 | a0001 | c0001 | t0202 | g0263 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0404 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01257 | hp1 | a0002 | c0003 | t0007 | g0190 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01257 | hp2 | a0002 | c0003 | t0010 | g0007 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01258 | hp1 | a0001 | c0001 | t0201 | g0266 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01258 | hp2 | a0002 | c0003 | t0010 | g0007 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01261 | hp2 | a0001 | c0001 | t0024 | g0211 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0162 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01346 | hp2 | a0001 | c0001 | t0159 | g0264 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01358 | hp1 | a0001 | c0001 | t0011 | g0054 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01358 | hp2 | a0003 | c0004 | t0187 | g0325 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01361 | hp1 | a0001 | c0001 | t0035 | g0210 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01361 | hp2 | a0001 | c0001 | t0058 | g0063 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01433 | hp1 | a0003 | c0004 | t0018 | g0410 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01433 | hp2 | a0001 | c0001 | t0089 | g0256 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01496 | hp1 | a0001 | c0001 | t0035 | g0206 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01496 | hp2 | a0002 | c0003 | t0128 | g0401 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01515 | hp1 | a0002 | c0003 | t0032 | g0121 | EUR | IBS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01515 | hp2 | a0002 | c0003 | t0207 | g0119 | EUR | IBS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01516 | hp1 | a0002 | c0003 | t0122 | g0199 | EUR | IBS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01516 | hp2 | a0001 | c0001 | t0057 | g0197 | EUR | IBS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01517 | hp1 | a0002 | c0003 | t0010 | g0198 | EUR | IBS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01517 | hp2 | a0002 | c0003 | t0032 | g0008 | EUR | IBS | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01884 | hp1 | a0009 | c0036 | t0099 | g0017 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01884 | hp2 | a0007 | c0012 | t0084 | g0113 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01891 | hp1 | a0001 | c0001 | t0228 | g0443 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01891 | hp2 | a0002 | c0003 | t0135 | g0114 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0067 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01934 | hp2 | a0006 | c0007 | t0006 | g0352 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01943 | hp1 | a0001 | c0002 | t0181 | g0221 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01943 | hp2 | a0001 | c0001 | t0011 | g0228 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01952 | hp2 | a0001 | c0001 | t0011 | g0258 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01975 | hp2 | a0008 | c0014 | t0046 | g0369 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0066 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0243 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01981 | hp1 | a0002 | c0003 | t0007 | g0226 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01981 | hp2 | a0001 | c0001 | t0155 | g0262 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01993 | hp1 | a0001 | c0001 | t0058 | g0061 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01993 | hp2 | a0001 | c0001 | t0180 | g0230 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0062 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02004 | hp2 | a0001 | c0001 | t0060 | g0333 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02015 | hp1 | a0001 | c0005 | t0003 | g0040 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02015 | hp2 | a0001 | c0002 | t0006 | g0143 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02027 | hp1 | a0001 | c0002 | t0195 | g0292 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02027 | hp2 | a0001 | c0001 | t0054 | g0416 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02040 | hp1 | a0001 | c0001 | t0186 | g0164 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02040 | hp2 | a0001 | c0001 | t0147 | g0229 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02055 | hp1 | a0002 | c0003 | t0028 | g0023 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02055 | hp2 | a0002 | c0010 | t0133 | g0203 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02056 | hp1 | a0001 | c0002 | t0004 | g0390 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02056 | hp2 | a0001 | c0001 | t0199 | g0151 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02071 | hp1 | a0001 | c0002 | t0148 | g0233 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02080 | hp1 | a0002 | c0003 | t0127 | g0222 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02080 | hp2 | a0001 | c0001 | t0173 | g0420 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02083 | hp1 | a0001 | c0002 | t0038 | g0301 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02083 | hp2 | a0001 | c0001 | t0054 | g0415 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02129 | hp1 | a0001 | c0002 | t0004 | g0280 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02129 | hp2 | a0001 | c0001 | t0154 | g0068 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02132 | hp1 | a0001 | c0001 | t0194 | g0057 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02132 | hp2 | a0001 | c0005 | t0179 | g0403 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02135 | hp1 | a0002 | c0003 | t0007 | g0069 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02145 | hp1 | a0001 | c0001 | t0104 | g0344 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02145 | hp2 | a0002 | c0010 | t0040 | g0010 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0060 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02148 | hp2 | a0001 | c0001 | t0012 | g0261 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0439 | EAS | CDX | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | CDX | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | CDX | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02165 | hp2 | a0001 | c0001 | t0144 | g0238 | EAS | CDX | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02257 | hp1 | a0003 | c0004 | t0028 | g0422 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02257 | hp2 | a0002 | c0003 | t0126 | g0129 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02258 | hp1 | a0002 | c0013 | t0085 | g0194 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02258 | hp2 | a0002 | c0010 | t0040 | g0010 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0059 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02273 | hp2 | a0001 | c0002 | t0177 | g0361 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02280 | hp1 | a0002 | c0009 | t0020 | g0383 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02280 | hp2 | a0002 | c0010 | t0044 | g0346 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02293 | hp1 | a0001 | c0001 | t0060 | g0270 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02293 | hp2 | a0001 | c0002 | t0012 | g0225 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0392 | AMR | PEL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02451 | hp1 | a0001 | c0001 | t0039 | g0016 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02451 | hp2 | a0002 | c0003 | t0067 | g0426 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02523 | hp1 | a0001 | c0001 | t0119 | g0042 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02523 | hp2 | a0001 | c0001 | t0192 | g0398 | EAS | KHV | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02572 | hp1 | a0003 | c0004 | t0041 | g0427 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02572 | hp2 | a0001 | c0006 | t0044 | g0181 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02602 | hp1 | a0001 | c0001 | t0070 | g0246 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02602 | hp2 | a0001 | c0002 | t0056 | g0319 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02615 | hp1 | a0002 | c0003 | t0139 | g0115 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02615 | hp2 | a0004 | c0020 | t0142 | g0409 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02622 | hp1 | a0003 | c0004 | t0225 | g0448 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02622 | hp2 | a0002 | c0019 | t0027 | g0418 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02630 | hp1 | a0001 | c0006 | t0043 | g0215 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02630 | hp2 | a0004 | c0011 | t0097 | g0371 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02647 | hp1 | a0001 | c0006 | t0137 | g0421 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02647 | hp2 | a0005 | c0008 | t0098 | g0338 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02683 | hp2 | a0001 | c0002 | t0026 | g0308 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02698 | hp1 | a0001 | c0001 | t0221 | g0161 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02698 | hp2 | a0001 | c0001 | t0068 | g0245 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02717 | hp1 | a0001 | c0002 | t0143 | g0326 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02717 | hp2 | a0001 | c0001 | t0030 | g0368 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02723 | hp1 | a0001 | c0006 | t0043 | g0331 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02723 | hp2 | a0015 | c0038 | t0052 | g0343 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02735 | hp1 | a0001 | c0002 | t0056 | g0320 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02735 | hp2 | a0002 | c0003 | t0010 | g0189 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02738 | hp1 | a0002 | c0003 | t0062 | g0146 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0247 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02809 | hp1 | a0001 | c0001 | t0103 | g0412 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02809 | hp2 | a0001 | c0001 | t0161 | g0110 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02818 | hp1 | a0002 | c0003 | t0212 | g0120 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02818 | hp2 | a0002 | c0035 | t0027 | g0433 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02886 | hp1 | a0001 | c0001 | t0101 | g0187 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02886 | hp2 | a0005 | c0008 | t0080 | g0031 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02895 | hp1 | a0002 | c0003 | t0047 | g0377 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02895 | hp2 | a0002 | c0009 | t0020 | g0385 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02896 | hp1 | a0002 | c0003 | t0093 | g0437 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02896 | hp2 | a0001 | c0001 | t0053 | g0435 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02897 | hp1 | a0001 | c0001 | t0053 | g0434 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02897 | hp2 | a0002 | c0003 | t0047 | g0376 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02922 | hp1 | a0001 | c0001 | t0213 | g0388 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02922 | hp2 | a0003 | c0004 | t0108 | g0341 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02965 | hp1 | a0001 | c0001 | t0166 | g0111 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02965 | hp2 | a0002 | c0013 | t0025 | g0105 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02970 | hp1 | a0003 | c0004 | t0018 | g0411 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02970 | hp2 | a0004 | c0011 | t0092 | g0366 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02976 | hp1 | a0007 | c0012 | t0037 | g0367 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02976 | hp2 | a0002 | c0019 | t0027 | g0402 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03017 | hp2 | a0002 | c0003 | t0112 | g0125 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03041 | hp1 | a0002 | c0003 | t0136 | g0347 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03041 | hp2 | a0003 | c0004 | t0018 | g0337 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03098 | hp1 | a0004 | c0020 | t0121 | g0032 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03098 | hp2 | a0003 | c0004 | t0041 | g0428 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03130 | hp1 | a0003 | c0004 | t0018 | g0033 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03130 | hp2 | a0003 | c0004 | t0138 | g0342 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03139 | hp1 | a0002 | c0010 | t0132 | g0205 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03139 | hp2 | a0002 | c0009 | t0227 | g0444 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03209 | hp1 | a0001 | c0006 | t0113 | g0328 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03209 | hp2 | a0003 | c0004 | t0028 | g0424 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03225 | hp1 | a0001 | c0005 | t0129 | g0413 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03225 | hp2 | a0001 | c0001 | t0039 | g0016 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03239 | hp1 | a0001 | c0001 | t0009 | g0251 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03239 | hp2 | a0001 | c0001 | t0229 | g0449 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03453 | hp1 | a0001 | c0001 | t0030 | g0335 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03453 | hp2 | a0005 | c0008 | t0079 | g0030 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03486 | hp1 | a0007 | c0012 | t0037 | g0332 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03486 | hp2 | a0007 | c0012 | t0076 | g0345 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03490 | hp1 | a0001 | c0001 | t0009 | g0158 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03490 | hp2 | a0002 | c0003 | t0145 | g0191 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03491 | hp1 | a0002 | c0003 | t0048 | g0003 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03491 | hp2 | a0001 | c0001 | t0075 | g0184 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03492 | hp1 | a0002 | c0003 | t0048 | g0003 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03492 | hp2 | a0001 | c0001 | t0009 | g0159 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03516 | hp1 | a0002 | c0003 | t0042 | g0219 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03516 | hp2 | a0016 | c0034 | t0167 | g0339 | AFR | ESN | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0336 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03540 | hp2 | a0003 | c0004 | t0226 | g0442 | AFR | GWD | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03579 | hp1 | a0002 | c0009 | t0020 | g0382 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03579 | hp2 | a0001 | c0005 | t0140 | g0432 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0242 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03654 | hp2 | a0001 | c0001 | t0125 | g0248 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03669 | hp1 | a0001 | c0001 | t0013 | g0160 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03669 | hp2 | a0001 | c0001 | t0017 | g0148 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03688 | hp1 | a0001 | c0001 | t0131 | g0196 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03688 | hp2 | a0001 | c0001 | t0208 | g0028 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03704 | hp1 | a0017 | c0021 | t0007 | g0192 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03704 | hp2 | a0001 | c0001 | t0077 | g0330 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03710 | hp1 | a0001 | c0002 | t0006 | g0177 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03710 | hp2 | a0002 | c0003 | t0123 | g0035 | SAS | PJL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03831 | hp1 | a0001 | c0001 | t0134 | g0329 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0406 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03834 | hp1 | a0002 | c0003 | t0210 | g0374 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03834 | hp2 | a0018 | c0029 | t0205 | g0405 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03927 | hp1 | a0001 | c0001 | t0184 | g0176 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03927 | hp2 | a0001 | c0002 | t0012 | g0302 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03942 | hp1 | a0001 | c0001 | t0068 | g0195 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03942 | hp2 | a0001 | c0002 | t0023 | g0304 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0253 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04115 | hp2 | a0001 | c0002 | t0059 | g0178 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0380 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0122 | SAS | BEB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04199 | hp1 | a0001 | c0001 | t0013 | g0389 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04199 | hp2 | a0001 | c0001 | t0059 | g0045 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0375 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04204 | hp2 | a0001 | c0001 | t0036 | g0116 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04228 | hp1 | a0005 | c0008 | t0088 | g0188 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG04228 | hp2 | a0002 | c0003 | t0118 | g0127 | SAS | STU | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18522 | hp1 | a0001 | c0006 | t0069 | g0445 | AFR | YRI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18522 | hp2 | a0001 | c0005 | t0071 | g0407 | AFR | YRI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18612 | hp1 | a0001 | c0001 | t0223 | g0441 | EAS | CHB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18612 | hp2 | a0002 | c0003 | t0029 | g0078 | EAS | CHB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18906 | hp1 | a0001 | c0006 | t0069 | g0446 | AFR | YRI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18906 | hp2 | a0002 | c0013 | t0025 | g0104 | AFR | YRI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18939 | hp2 | a0001 | c0002 | t0022 | g0201 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18940 | hp1 | a0002 | c0003 | t0015 | g0002 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18940 | hp2 | a0001 | c0001 | t0012 | g0408 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18941 | hp2 | a0001 | c0001 | t0182 | g0322 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18942 | hp1 | a0001 | c0001 | t0215 | g0091 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18944 | hp2 | a0006 | c0007 | t0026 | g0101 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18945 | hp1 | a0001 | c0001 | t0016 | g0237 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18945 | hp2 | a0001 | c0001 | t0033 | g0084 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18946 | hp1 | a0002 | c0003 | t0007 | g0097 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18946 | hp2 | a0001 | c0002 | t0165 | g0273 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18947 | hp1 | a0001 | c0002 | t0061 | g0281 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18947 | hp2 | a0001 | c0001 | t0021 | g0168 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18948 | hp1 | a0001 | c0002 | t0063 | g0288 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18948 | hp2 | a0001 | c0001 | t0046 | g0093 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18949 | hp1 | a0002 | c0003 | t0014 | g0070 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18951 | hp1 | a0001 | c0002 | t0004 | g0309 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18951 | hp2 | a0002 | c0003 | t0117 | g0077 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18953 | hp1 | a0001 | c0001 | t0045 | g0015 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18953 | hp2 | a0001 | c0002 | t0082 | g0307 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18954 | hp1 | a0001 | c0001 | t0191 | g0265 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18954 | hp2 | a0006 | c0007 | t0008 | g0012 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18956 | hp1 | a0001 | c0001 | t0031 | g0170 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18957 | hp1 | a0002 | c0003 | t0007 | g0074 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18957 | hp2 | a0001 | c0002 | t0214 | g0290 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18959 | hp1 | a0001 | c0002 | t0200 | g0279 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18959 | hp2 | a0001 | c0002 | t0146 | g0300 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18960 | hp1 | a0001 | c0002 | t0004 | g0098 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18960 | hp2 | a0001 | c0001 | t0031 | g0086 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18962 | hp2 | a0001 | c0005 | t0073 | g0094 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18963 | hp1 | a0001 | c0002 | t0151 | g0296 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18963 | hp2 | a0001 | c0001 | t0017 | g0149 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18964 | hp2 | a0001 | c0002 | t0152 | g0318 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18965 | hp2 | a0001 | c0002 | t0034 | g0175 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18966 | hp1 | a0001 | c0001 | t0055 | g0395 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18966 | hp2 | a0001 | c0002 | t0004 | g0310 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18967 | hp1 | a0002 | c0003 | t0014 | g0124 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18967 | hp2 | a0001 | c0001 | t0031 | g0087 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18968 | hp1 | a0001 | c0002 | t0190 | g0317 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18968 | hp2 | a0001 | c0001 | t0023 | g0004 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18971 | hp1 | a0001 | c0002 | t0004 | g0316 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18973 | hp1 | a0002 | c0003 | t0015 | g0002 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18973 | hp2 | a0001 | c0001 | t0211 | g0414 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18975 | hp1 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18975 | hp2 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18977 | hp2 | a0001 | c0001 | t0206 | g0400 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18978 | hp1 | a0001 | c0002 | t0004 | g0106 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18978 | hp2 | a0001 | c0001 | t0216 | g0090 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18979 | hp1 | a0001 | c0001 | t0023 | g0004 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18980 | hp1 | a0002 | c0015 | t0183 | g0072 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18980 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18981 | hp1 | a0002 | c0003 | t0014 | g0130 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18981 | hp2 | a0001 | c0001 | t0065 | g0157 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18982 | hp1 | a0002 | c0003 | t0019 | g0152 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18984 | hp2 | a0001 | c0001 | t0033 | g0088 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18985 | hp1 | a0001 | c0001 | t0168 | g0171 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18985 | hp2 | a0001 | c0002 | t0169 | g0291 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18986 | hp1 | a0001 | c0001 | t0197 | g0259 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18986 | hp2 | a0001 | c0005 | t0072 | g0044 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18987 | hp1 | a0001 | c0001 | t0021 | g0167 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18987 | hp2 | a0006 | c0007 | t0008 | g0351 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18988 | hp2 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18989 | hp1 | a0002 | c0003 | t0015 | g0133 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18989 | hp2 | a0002 | c0003 | t0007 | g0096 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18991 | hp1 | a0002 | c0003 | t0007 | g0006 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18991 | hp2 | a0001 | c0001 | t0011 | g0049 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18993 | hp1 | a0001 | c0005 | t0064 | g0359 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18993 | hp2 | a0019 | c0030 | t0109 | g0231 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18994 | hp1 | a0001 | c0001 | t0217 | g0092 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18994 | hp2 | a0001 | c0002 | t0012 | g0272 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18995 | hp1 | a0001 | c0002 | t0006 | g0095 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18995 | hp2 | a0001 | c0001 | t0156 | g0268 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18997 | hp1 | a0001 | c0001 | t0172 | g0038 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18997 | hp2 | a0001 | c0002 | t0066 | g0202 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18998 | hp2 | a0002 | c0003 | t0019 | g0153 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18999 | hp1 | a0001 | c0001 | t0008 | g0353 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19000 | hp1 | a0002 | c0003 | t0015 | g0132 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0355 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19002 | hp1 | a0001 | c0001 | t0017 | g0166 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19003 | hp1 | a0001 | c0017 | t0022 | g0200 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19003 | hp2 | a0001 | c0001 | t0033 | g0082 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19004 | hp2 | a0001 | c0002 | t0153 | g0321 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19005 | hp1 | a0001 | c0001 | t0185 | g0391 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19007 | hp1 | a0001 | c0002 | t0038 | g0306 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19009 | hp1 | a0001 | c0001 | t0170 | g0327 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19009 | hp2 | a0001 | c0001 | t0065 | g0156 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19010 | hp1 | a0001 | c0005 | t0003 | g0358 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0393 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19011 | hp1 | a0002 | c0003 | t0015 | g0002 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19012 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19030 | hp1 | a0003 | c0004 | t0107 | g0436 | AFR | LWK | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19030 | hp2 | a0005 | c0008 | t0090 | g0204 | AFR | LWK | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19043 | hp1 | a0002 | c0003 | t0120 | g0134 | AFR | LWK | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19043 | hp2 | a0002 | c0013 | t0025 | g0018 | AFR | LWK | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19054 | hp1 | a0001 | c0001 | t0045 | g0015 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19054 | hp2 | a0001 | c0001 | t0164 | g0354 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19056 | hp1 | a0002 | c0003 | t0010 | g0071 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0356 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19057 | hp2 | a0001 | c0001 | t0158 | g0397 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19058 | hp2 | a0001 | c0001 | t0209 | g0381 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19060 | hp1 | a0001 | c0001 | t0022 | g0169 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19062 | hp1 | a0001 | c0001 | t0016 | g0235 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19063 | hp1 | a0006 | c0007 | t0026 | g0102 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19063 | hp2 | a0001 | c0027 | t0029 | g0299 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19064 | hp2 | a0001 | c0001 | t0009 | g0109 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19065 | hp1 | a0002 | c0015 | t0193 | g0073 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19065 | hp2 | a0001 | c0001 | t0023 | g0051 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19066 | hp1 | a0001 | c0001 | t0021 | g0165 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19067 | hp1 | a0001 | c0001 | t0008 | g0360 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19067 | hp2 | a0001 | c0002 | t0081 | g0312 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19068 | hp1 | a0001 | c0002 | t0188 | g0363 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19070 | hp1 | a0006 | c0007 | t0008 | g0012 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19070 | hp2 | a0001 | c0002 | t0006 | g0277 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19074 | hp1 | a0001 | c0001 | t0204 | g0085 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0056 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19076 | hp1 | a0001 | c0002 | t0063 | g0287 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19076 | hp2 | a0020 | c0028 | t0002 | g0257 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19077 | hp1 | a0001 | c0002 | t0061 | g0283 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19077 | hp2 | a0002 | c0003 | t0029 | g0079 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19078 | hp1 | a0001 | c0002 | t0083 | g0193 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19078 | hp2 | a0001 | c0001 | t0055 | g0173 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19079 | hp1 | a0002 | c0003 | t0007 | g0075 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19079 | hp2 | a0001 | c0001 | t0022 | g0172 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19080 | hp2 | a0001 | c0001 | t0178 | g0286 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19081 | hp1 | a0001 | c0002 | t0006 | g0289 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19081 | hp2 | a0001 | c0001 | t0017 | g0150 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19082 | hp1 | a0001 | c0001 | t0016 | g0239 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19082 | hp2 | a0001 | c0001 | t0198 | g0396 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19084 | hp2 | a0002 | c0003 | t0007 | g0076 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19085 | hp1 | a0001 | c0001 | t0150 | g0107 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19085 | hp2 | a0002 | c0003 | t0014 | g0128 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19086 | hp1 | a0001 | c0005 | t0003 | g0357 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19087 | hp1 | a0001 | c0002 | t0034 | g0278 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19087 | hp2 | a0001 | c0005 | t0003 | g0041 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19088 | hp2 | a0001 | c0002 | t0066 | g0118 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19090 | hp1 | a0001 | c0002 | t0012 | g0271 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19091 | hp1 | a0001 | c0001 | t0157 | g0260 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19091 | hp2 | a0001 | c0002 | t0171 | g0362 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19240 | hp1 | a0003 | c0004 | t0052 | g0340 | AFR | YRI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA19240 | hp2 | a0004 | c0011 | t0094 | g0370 | AFR | YRI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20129 | hp1 | a0021 | c0031 | t0219 | g0112 | AFR | ASW | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20129 | hp2 | a0004 | c0011 | t0096 | g0034 | AFR | ASW | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20752 | hp1 | a0022 | c0039 | t0014 | g0142 | EUR | TSI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0137 | EUR | TSI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20805 | hp1 | a0001 | c0005 | t0130 | g0431 | EUR | TSI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20805 | hp2 | a0002 | c0003 | t0162 | g0379 | EUR | TSI | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20905 | hp1 | a0001 | c0002 | t0006 | g0323 | SAS | GIH | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20905 | hp2 | a0001 | c0002 | t0176 | g0311 | SAS | GIH | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01123 | hp1 | a0002 | c0003 | t0124 | g0123 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG01123 | hp2 | a0001 | c0018 | t0078 | g0207 | AMR | CLM | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02109 | hp1 | a0009 | c0037 | t0114 | g0386 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02109 | hp2 | a0002 | c0009 | t0020 | g0425 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02486 | hp1 | a0001 | c0001 | t0102 | g0350 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02486 | hp2 | a0003 | c0004 | t0042 | g0423 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02559 | hp1 | a0014 | c0025 | t0224 | g0447 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG02559 | hp2 | a0001 | c0005 | t0141 | g0348 | AFR | ACB | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03471 | hp1 | a0002 | c0016 | t0051 | g0216 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
HG03471 | hp2 | a0001 | c0001 | t0091 | g0430 | AFR | MSL | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20300 | hp1 | a0001 | c0002 | t0034 | g0282 | AFR | USA | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA20300 | hp2 | a0001 | c0001 | t0024 | g0135 | AFR | USA | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA21309 | hp1 | a0004 | c0011 | t0095 | g0372 | AFR | LWK | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
NA21309 | hp2 | a0003 | c0004 | t0222 | g0022 | AFR | LWK | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
homoSapiens | chm13v2 | a0023 | c0026 | t0016 | g0334 | REF | REF | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
homoSapiens | grch38p0 | a0005 | c0008 | t0111 | g0419 | REF | REF | MEAK7_chr16_84471355_84509659 | MEAK7 | chr16 | 84471355 | 84509659 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:84479956 | G | A | 1 | a0008 | 3 | HG01070.hp1 HG01071.hp2 HG01975.hp2 |
missense_variant | MODERATE | c.1328C>T | p.Ser443Leu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1412/5013 | 1328/1371 | 443/456 | chr16 | 84479956 | |||
chr16:84479971 | T | C | 1 | a0019 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.1313A>G | p.Glu438Gly | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1397/5013 | 1313/1371 | 438/456 | chr16 | 84479971 | |||
chr16:84479998 | G | A | 1 | a0017 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1286C>T | p.Ala429Val | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1370/5013 | 1286/1371 | 429/456 | chr16 | 84479998 | |||
chr16:84480599 | G | A | 1 | a0010 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1187C>T | p.Ser396Leu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/8 | 1271/5013 | 1187/1371 | 396/456 | chr16 | 84480599 | |||
chr16:84480629 | G | A | 1 | a0014 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1157C>T | p.Thr386Met | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/8 | 1241/5013 | 1157/1371 | 386/456 | chr16 | 84480629 | |||
chr16:84480699 | C | G | 1 | a0020 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1087G>C | p.Gly363Arg | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/8 | 1171/5013 | 1087/1371 | 363/456 | chr16 | 84480699 | |||
chr16:84482647 | T | A | 1 | a0018 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1022A>T | p.Tyr341Phe | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/8 | 1106/5013 | 1022/1371 | 341/456 | chr16 | 84482647 | |||
chr16:84486822 | G | C | 1 | a0011 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.767C>G | p.Ala256Gly | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 851/5013 | 767/1371 | 256/456 | chr16 | 84486822 | |||
chr16:84486890 | C | G | 1 | a0007 | 4 | HG01884.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.699G>C | p.Glu233Asp | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 783/5013 | 699/1371 | 233/456 | chr16 | 84486890 | |||
chr16:84486900 | A | G | 1 | a0006 | 6 | HG01934.hp2 NA18944.hp2 NA18954.hp2 others(3): Show |
missense_variant | MODERATE | c.689T>C | p.Leu230Pro | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 773/5013 | 689/1371 | 230/456 | chr16 | 84486900 | |||
chr16:84486931 | T | C | 21 | a0001 a0002 a0003 others(18): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
missense_variant | MODERATE | c.658A>G | p.Ile220Val | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 742/5013 | 658/1371 | 220/456 | chr16 | 84486931 | |||
chr16:84487013 | G | C | 1 | a0013 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.576C>G | p.Asp192Glu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 660/5013 | 576/1371 | 192/456 | chr16 | 84487013 | |||
chr16:84489284 | G | C | 1 | a0021 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.523C>G | p.Leu175Val | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/8 | 607/5013 | 523/1371 | 175/456 | chr16 | 84489284 | |||
chr16:84489291 | G | C | 9 | a0001 a0006 a0009 others(6): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
missense_variant | MODERATE | c.516C>G | p.Asp172Glu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/8 | 600/5013 | 516/1371 | 172/456 | chr16 | 84489291 | |||
chr16:84489419 | T | C | 2 | a0012 a0022 |
2 | HG00733.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.388A>G | p.Thr130Ala | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/8 | 472/5013 | 388/1371 | 130/456 | chr16 | 84489419 | |||
chr16:84495776 | G | C | 3 | a0003 a0013 a0016 |
20 | HG00735.hp1 HG01255.hp1 HG01358.hp2 others(17): Show |
missense_variant | MODERATE | c.291C>G | p.His97Gln | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/8 | 375/5013 | 291/1371 | 97/456 | chr16 | 84495776 | |||
chr16:84495781 | A | C | 1 | a0006 | 6 | HG01934.hp2 NA18944.hp2 NA18954.hp2 others(3): Show |
missense_variant | MODERATE | c.286T>G | p.Ser96Ala | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/8 | 370/5013 | 286/1371 | 96/456 | chr16 | 84495781 | |||
chr16:84497956 | G | A | 1 | a0009 | 2 | HG01884.hp1 HG02109.hp1 |
missense_variant | MODERATE | c.131C>T | p.Ser44Phe | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/8 | 215/5013 | 131/1371 | 44/456 | chr16 | 84497956 | |||
chr16:84497971 | T | C | 1 | a0015 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.116A>G | p.Asn39Ser | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/8 | 200/5013 | 116/1371 | 39/456 | chr16 | 84497971 | |||
chr16:84497989 | G | A | 1 | a0022 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.98C>T | p.Ser33Leu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/8 | 182/5013 | 98/1371 | 33/456 | chr16 | 84497989 | |||
chr16:84498058 | C | A | 1 | a0004 | 7 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(4): Show |
missense_variant | MODERATE | c.29G>T | p.Arg10Leu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/8 | 113/5013 | 29/1371 | 10/456 | chr16 | 84498058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:84479922 | G | A | 1 | a0014c0025 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1362C>T | p.Asp454Asp | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1446/5013 | 1362/1371 | 454/456 | chr16 | 84479922 | |||
chr16:84482598 | G | A | 1 | a0001c0018 | 2 | HG00280.hp1 HG01123.hp2 |
synonymous_variant | LOW | c.1071C>T | p.Asn357Asn | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/8 | 1155/5013 | 1071/1371 | 357/456 | chr16 | 84482598 | |||
chr16:84482601 | C | T | 1 | a0002c0016 | 2 | HG00639.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1068G>A | p.Pro356Pro | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/8 | 1152/5013 | 1068/1371 | 356/456 | chr16 | 84482601 | |||
chr16:84482703 | G | A | 8 | a0001c0001 a0001c0017 a0001c0018 others(5): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
synonymous_variant | LOW | c.966C>T | p.Asn322Asn | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/8 | 1050/5013 | 966/1371 | 322/456 | chr16 | 84482703 | |||
chr16:84486686 | C | T | 8 | a0001c0002 a0001c0006 a0001c0017 others(5): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
synonymous_variant | LOW | c.903G>A | p.Lys301Lys | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 987/5013 | 903/1371 | 301/456 | chr16 | 84486686 | |||
chr16:84486719 | T | C | 18 | a0001c0001 a0001c0002 a0001c0005 others(15): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
synonymous_variant | LOW | c.870A>G | p.Gly290Gly | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 954/5013 | 870/1371 | 290/456 | chr16 | 84486719 | |||
chr16:84486776 | C | T | 1 | a0002c0010 | 5 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(2): Show |
synonymous_variant | LOW | c.813G>A | p.Ser271Ser | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 897/5013 | 813/1371 | 271/456 | chr16 | 84486776 | |||
chr16:84486821 | G | A | 1 | a0002c0035 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.768C>T | p.Ala256Ala | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 852/5013 | 768/1371 | 256/456 | chr16 | 84486821 | |||
chr16:84486853 | G | A | 3 | a0002c0009 a0002c0013 a0014c0025 |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
synonymous_variant | LOW | c.736C>T | p.Leu246Leu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/8 | 820/5013 | 736/1371 | 246/456 | chr16 | 84486853 | |||
chr16:84489318 | C | T | 1 | a0002c0015 | 2 | NA18980.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.489G>A | p.Gln163Gln | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/8 | 573/5013 | 489/1371 | 163/456 | chr16 | 84489318 | |||
chr16:84495697 | T | G | 4 | a0001c0006 a0002c0009 a0002c0019 others(1): Show |
16 | HG01175.hp2 HG02109.hp2 HG02280.hp1 others(13): Show |
synonymous_variant | LOW | c.370A>C | p.Arg124Arg | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/8 | 454/5013 | 370/1371 | 124/456 | chr16 | 84495697 | |||
chr16:84495871 | G | A | 2 | a0002c0019 a0002c0035 |
3 | HG02622.hp2 HG02818.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.196C>T | p.Leu66Leu | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/8 | 280/5013 | 196/1371 | 66/456 | chr16 | 84495871 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:84476358 | G | A | 65 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(62): Show |
127 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*3555C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3555 | chr16 | 84476358 | ||||||
chr16:84476383 | G | A | 1 | a0001c0001t0077 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3530C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3530 | chr16 | 84476383 | ||||||
chr16:84476385 | T | G | 102 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(99): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*3528A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3528 | chr16 | 84476385 | ||||||
chr16:84476416 | G | C | 43 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(40): Show |
83 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3497C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3497 | chr16 | 84476416 | ||||||
chr16:84476452 | T | A | 2 | a0007c0012t0037 a0007c0012t0076 |
3 | HG02976.hp1 HG03486.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3461A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3461 | chr16 | 84476452 | ||||||
chr16:84476467 | T | C | 2 | a0002c0003t0136 a0002c0003t0139 |
2 | HG02615.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3446A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3446 | chr16 | 84476467 | ||||||
chr16:84476609 | G | A | 2 | a0001c0005t0130 a0002c0003t0145 |
2 | HG03490.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3304C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3304 | chr16 | 84476609 | ||||||
chr16:84476649 | C | T | 13 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(10): Show |
43 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3264G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3264 | chr16 | 84476649 | ||||||
chr16:84476689 | C | T | 1 | a0002c0003t0210 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3224G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3224 | chr16 | 84476689 | ||||||
chr16:84476713 | C | T | 3 | a0003c0004t0052 a0003c0004t0138 a0015c0038t0052 |
3 | HG02723.hp2 HG03130.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3200G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3200 | chr16 | 84476713 | ||||||
chr16:84476758 | A | C | 42 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0023 others(39): Show |
71 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3155T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3155 | chr16 | 84476758 | ||||||
chr16:84476800 | G | A | 4 | a0001c0001t0178 a0001c0001t0197 a0001c0027t0029 others(1): Show |
5 | NA18612.hp2 NA18986.hp1 NA19063.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3113C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3113 | chr16 | 84476800 | ||||||
chr16:84476826 | G | C | 1 | a0001c0002t0063 | 2 | NA18948.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3087C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3087 | chr16 | 84476826 | ||||||
chr16:84476826 | G | T | 1 | a0001c0002t0056 | 2 | HG02602.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3087C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 3087 | chr16 | 84476826 | ||||||
chr16:84476943 | G | A | 1 | a0001c0001t0180 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2970C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2970 | chr16 | 84476943 | ||||||
chr16:84476976 | C | G | 2 | a0001c0005t0129 a0009c0036t0099 |
2 | HG01884.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2937G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2937 | chr16 | 84476976 | ||||||
chr16:84477025 | A | G | 79 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(76): Show |
144 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2888T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2888 | chr16 | 84477025 | ||||||
chr16:84477050 | C | G | 3 | a0003c0004t0052 a0003c0004t0138 a0015c0038t0052 |
3 | HG02723.hp2 HG03130.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2863G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2863 | chr16 | 84477050 | ||||||
chr16:84477064 | G | A | 3 | a0001c0002t0061 a0001c0002t0189 a0001c0002t0200 |
4 | HG00438.hp1 NA18947.hp1 NA18959.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2849C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2849 | chr16 | 84477064 | ||||||
chr16:84477068 | T | A | 1 | a0004c0020t0142 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2845A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2845 | chr16 | 84477068 | ||||||
chr16:84477103 | C | G | 1 | a0003c0004t0226 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2810G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2810 | chr16 | 84477103 | ||||||
chr16:84477169 | A | C | 14 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(11): Show |
44 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2744T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2744 | chr16 | 84477169 | ||||||
chr16:84477175 | G | A | 147 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(144): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*2738C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2738 | chr16 | 84477175 | ||||||
chr16:84477186 | C | T | 1 | a0001c0002t0082 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2727 | chr16 | 84477186 | ||||||
chr16:84477214 | G | T | 33 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(30): Show |
69 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2699C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2699 | chr16 | 84477214 | ||||||
chr16:84477223 | C | A | 1 | a0001c0001t0198 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2690G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2690 | chr16 | 84477223 | ||||||
chr16:84477243 | G | A | 1 | a0002c0010t0133 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2670C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2670 | chr16 | 84477243 | ||||||
chr16:84477312 | C | T | 1 | a0001c0006t0113 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2601G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2601 | chr16 | 84477312 | ||||||
chr16:84477411 | G | C | 1 | a0001c0002t0190 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2502C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2502 | chr16 | 84477411 | ||||||
chr16:84477487 | G | C | 14 | a0001c0001t0053 a0001c0001t0100 a0001c0001t0101 others(11): Show |
20 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2426C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2426 | chr16 | 84477487 | ||||||
chr16:84477489 | C | G | 2 | a0002c0003t0136 a0002c0003t0139 |
2 | HG02615.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2424G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2424 | chr16 | 84477489 | ||||||
chr16:84477564 | T | A | 4 | a0001c0001t0022 a0001c0002t0022 a0001c0002t0066 others(1): Show |
6 | NA18939.hp2 NA18997.hp2 NA19003.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2349A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2349 | chr16 | 84477564 | ||||||
chr16:84477571 | C | T | 2 | a0001c0002t0152 a0002c0013t0085 |
2 | HG02258.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2342G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2342 | chr16 | 84477571 | ||||||
chr16:84477576 | A | ACAAATTT others(313): Show |
1 | a0003c0004t0108 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(316): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(314): Show |
1 | a0001c0001t0182 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(317): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(314): Show |
5 | a0001c0001t0060 a0001c0001t0067 a0001c0001t0102 others(2): Show |
6 | HG01099.hp1 HG01175.hp1 HG02004.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(317): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(315): Show |
1 | a0001c0017t0175 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(318): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(315): Show |
6 | a0001c0001t0159 a0001c0001t0213 a0002c0003t0120 others(3): Show |
6 | HG01346.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(318): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(316): Show |
8 | a0001c0001t0144 a0001c0001t0150 a0001c0001t0158 others(5): Show |
8 | HG00544.hp2 HG02165.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(319): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(317): Show |
3 | a0001c0001t0173 a0001c0002t0110 a0001c0002t0143 |
3 | HG00609.hp1 HG02080.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(320): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(318): Show |
3 | a0001c0001t0203 a0002c0015t0183 a0002c0015t0193 |
3 | HG00621.hp1 NA18980.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(321): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(319): Show |
1 | a0001c0001t0104 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(322): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(320): Show |
1 | a0001c0001t0192 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(323): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(322): Show |
1 | a0001c0002t0181 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(325): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(323): Show |
2 | a0001c0001t0157 a0001c0001t0202 |
2 | HG01256.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(326): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(324): Show |
3 | a0001c0001t0156 a0001c0001t0191 a0001c0001t0201 |
3 | HG01258.hp1 NA18954.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(327): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477576 | A | ACAAATTT others(325): Show |
1 | a0001c0001t0155 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336_*2337insGCCG others(328): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2336 | chr16 | 84477576 | ||||||
chr16:84477595 | C | T | 259 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(256): Show |
465 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(462): Show |
3_prime_UTR_variant | MODIFIER | c.*2318G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2318 | chr16 | 84477595 | ||||||
chr16:84477602 | C | T | 6 | a0001c0002t0171 a0001c0002t0177 a0001c0002t0188 others(3): Show |
6 | HG02273.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2311G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2311 | chr16 | 84477602 | ||||||
chr16:84477622 | T | TGA | 78 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(75): Show |
143 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2289_*2290dupTC | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2290 | chr16 | 84477622 | ||||||
chr16:84477625 | T | G | 5 | a0001c0001t0057 a0002c0003t0047 a0002c0003t0062 others(2): Show |
7 | HG00099.hp1 HG01255.hp2 HG01516.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2288A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2288 | chr16 | 84477625 | ||||||
chr16:84477654 | T | C | 49 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0023 others(46): Show |
80 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2259A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2259 | chr16 | 84477654 | ||||||
chr16:84477715 | C | A | 1 | a0002c0003t0145 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2198 | chr16 | 84477715 | ||||||
chr16:84477719 | G | C | 147 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(144): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*2194C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2194 | chr16 | 84477719 | ||||||
chr16:84477753 | T | G | 2 | a0002c0015t0183 a0002c0015t0193 |
2 | NA18980.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2160A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2160 | chr16 | 84477753 | ||||||
chr16:84477782 | G | A | 150 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(147): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*2131C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2131 | chr16 | 84477782 | ||||||
chr16:84477790 | A | T | 105 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(102): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2123T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2123 | chr16 | 84477790 | ||||||
chr16:84477803 | C | G | 1 | a0001c0001t0198 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2110 | chr16 | 84477803 | ||||||
chr16:84477859 | C | G | 107 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(104): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*2054G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2054 | chr16 | 84477859 | ||||||
chr16:84477879 | A | C | 115 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(112): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2034T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2034 | chr16 | 84477879 | ||||||
chr16:84477976 | C | T | 7 | a0002c0010t0040 a0002c0019t0027 a0002c0035t0027 others(4): Show |
9 | HG02145.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1937 | chr16 | 84477976 | ||||||
chr16:84477991 | G | A | 1 | a0001c0001t0204 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1922 | chr16 | 84477991 | ||||||
chr16:84478009 | A | C | 1 | a0002c0003t0145 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1904T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1904 | chr16 | 84478009 | ||||||
chr16:84478049 | A | AT | 164 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(161): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*1863dupA | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1863 | chr16 | 84478049 | ||||||
chr16:84478049 | A | ATT | 5 | a0001c0001t0030 a0001c0001t0045 a0001c0002t0151 others(2): Show |
8 | HG02027.hp1 HG02717.hp2 HG03453.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1862_*1863dupAA | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1863 | chr16 | 84478049 | ||||||
chr16:84478072 | A | G | 1 | a0003c0004t0107 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1841 | chr16 | 84478072 | ||||||
chr16:84478088 | G | A | 1 | a0001c0001t0154 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1825C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1825 | chr16 | 84478088 | ||||||
chr16:84478110 | T | TAAAAAAC others(314): Show |
1 | a0001c0005t0130 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1802_*1803insTTTT others(317): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1802 | chr16 | 84478110 | ||||||
chr16:84478152 | C | A | 1 | a0001c0001t0161 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1761G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1761 | chr16 | 84478152 | ||||||
chr16:84478205 | C | T | 2 | a0001c0001t0068 a0001c0001t0208 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1708G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1708 | chr16 | 84478205 | ||||||
chr16:84478236 | A | G | 1 | a0001c0002t0056 | 2 | HG02602.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1677T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1677 | chr16 | 84478236 | ||||||
chr16:84478248 | A | C | 1 | a0005c0008t0079 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1665T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1665 | chr16 | 84478248 | ||||||
chr16:84478327 | G | T | 2 | a0001c0005t0130 a0002c0003t0145 |
2 | HG03490.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1586C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1586 | chr16 | 84478327 | ||||||
chr16:84478425 | G | T | 1 | a0004c0011t0095 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1488C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1488 | chr16 | 84478425 | ||||||
chr16:84478447 | C | T | 1 | a0001c0001t0091 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1466G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1466 | chr16 | 84478447 | ||||||
chr16:84478455 | T | C | 2 | a0001c0005t0130 a0002c0003t0145 |
2 | HG03490.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1458A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1458 | chr16 | 84478455 | ||||||
chr16:84478457 | T | C | 2 | a0001c0005t0130 a0002c0003t0145 |
2 | HG03490.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1456A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1456 | chr16 | 84478457 | ||||||
chr16:84478537 | G | A | 1 | a0001c0005t0130 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1376 | chr16 | 84478537 | ||||||
chr16:84478610 | G | A | 2 | a0001c0005t0130 a0002c0003t0145 |
2 | HG03490.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1303C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1303 | chr16 | 84478610 | ||||||
chr16:84478620 | C | T | 1 | a0001c0001t0134 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1293G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1293 | chr16 | 84478620 | ||||||
chr16:84478651 | C | G | 1 | a0001c0005t0071 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1262G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1262 | chr16 | 84478651 | ||||||
chr16:84478707 | G | C | 1 | a0001c0002t0165 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1206 | chr16 | 84478707 | ||||||
chr16:84478722 | C | G | 259 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(256): Show |
465 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(462): Show |
3_prime_UTR_variant | MODIFIER | c.*1191G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1191 | chr16 | 84478722 | ||||||
chr16:84478733 | G | A | 2 | a0001c0005t0130 a0002c0003t0145 |
2 | HG03490.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1180C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1180 | chr16 | 84478733 | ||||||
chr16:84478750 | C | T | 1 | a0002c0010t0040 | 2 | HG02145.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1163G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1163 | chr16 | 84478750 | ||||||
chr16:84478795 | G | T | 1 | a0001c0001t0216 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1118 | chr16 | 84478795 | ||||||
chr16:84478908 | C | T | 1 | a0002c0003t0032 | 3 | HG01168.hp2 HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1005G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 1005 | chr16 | 84478908 | ||||||
chr16:84478954 | A | C | 3 | a0001c0001t0185 a0001c0001t0194 a0001c0005t0149 |
3 | HG00423.hp1 HG02132.hp1 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*959T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 959 | chr16 | 84478954 | ||||||
chr16:84478972 | G | A | 47 | a0001c0001t0024 a0001c0001t0031 a0001c0001t0033 others(44): Show |
54 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*941C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 941 | chr16 | 84478972 | ||||||
chr16:84479219 | T | C | 3 | a0001c0001t0039 a0001c0001t0091 a0014c0025t0224 |
4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*694A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 694 | chr16 | 84479219 | ||||||
chr16:84479243 | C | T | 7 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0055 others(4): Show |
16 | HG00597.hp1 HG00597.hp2 HG03669.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 670 | chr16 | 84479243 | ||||||
chr16:84479374 | T | G | 1 | a0002c0003t0145 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 539 | chr16 | 84479374 | ||||||
chr16:84479388 | A | G | 1 | a0001c0005t0129 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*525T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 525 | chr16 | 84479388 | ||||||
chr16:84479390 | G | GCTAATGC others(12): Show |
8 | a0001c0001t0068 a0001c0001t0087 a0001c0001t0206 others(5): Show |
11 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*522dupGGAATT others(13): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(31): Show |
11 | a0001c0001t0008 a0001c0001t0100 a0001c0001t0208 others(8): Show |
21 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*485_*522dupGGAATT others(32): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(50): Show |
2 | a0002c0003t0127 a0005c0008t0088 |
2 | HG02080.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*466_*522dupGGAATT others(51): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(69): Show |
7 | a0001c0001t0089 a0001c0001t0101 a0001c0001t0102 others(4): Show |
8 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*522dupGGAATT others(70): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(88): Show |
4 | a0001c0001t0103 a0001c0001t0104 a0002c0003t0042 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*428_*522dupGGAATT others(89): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(107): Show |
1 | a0001c0001t0213 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409_*522dupGGAATT others(108): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(202): Show |
1 | a0001c0002t0214 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522_*523insGGAATT others(203): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(221): Show |
1 | a0001c0001t0105 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522_*523insGGAATT others(222): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | G | GCTAATGC others(240): Show |
1 | a0002c0003t0128 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522_*523insGGAATT others(241): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 522 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(12): Show |
G | 33 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0033 others(30): Show |
58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*522delGGAATT others(13): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 504 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(31): Show |
G | 48 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0017 others(45): Show |
103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*485_*522delGGAATT others(32): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 485 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(50): Show |
G | 36 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(33): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*522delGGAATT others(51): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 466 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(69): Show |
G | 38 | a0001c0001t0002 a0001c0001t0031 a0001c0001t0035 others(35): Show |
61 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*522delGGAATT others(70): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 447 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(88): Show |
G | 14 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0055 others(11): Show |
22 | HG00735.hp1 HG01192.hp2 HG01243.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*428_*522delGGAATT others(89): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 428 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(107): Show |
G | 14 | a0001c0001t0054 a0001c0001t0154 a0001c0001t0155 others(11): Show |
15 | HG01099.hp1 HG01346.hp2 HG01981.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*409_*522del | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 409 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(126): Show |
G | 6 | a0001c0001t0150 a0001c0005t0072 a0001c0005t0149 others(3): Show |
6 | HG00423.hp1 HG02615.hp2 HG03017.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*390_*522del | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 390 | chr16 | 84479390 | ||||||
chr16:84479390 | GCTAATGC others(145): Show |
G | 2 | a0001c0001t0144 a0002c0003t0145 |
2 | HG02165.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371_*522del | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 371 | chr16 | 84479390 | ||||||
chr16:84479402 | G | GGAATTCC others(12): Show |
3 | a0003c0004t0052 a0003c0004t0138 a0015c0038t0052 |
3 | HG02723.hp2 HG03130.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510_*511insTGCTGG others(13): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 510 | chr16 | 84479402 | ||||||
chr16:84479439 | C | T | 1 | a0001c0001t0184 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*474G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 474 | chr16 | 84479439 | ||||||
chr16:84479460 | G | C | 1 | a0001c0001t0215 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 453 | chr16 | 84479460 | ||||||
chr16:84479478 | G | GGAATTCC others(12): Show |
1 | a0001c0005t0129 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*434_*435insTGCTGA others(13): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 434 | chr16 | 84479478 | ||||||
chr16:84479479 | G | C | 2 | a0001c0001t0216 a0001c0001t0217 |
2 | NA18978.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*434C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 434 | chr16 | 84479479 | ||||||
chr16:84479497 | G | A | 5 | a0001c0005t0129 a0002c0009t0020 a0002c0009t0218 others(2): Show |
8 | HG01175.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*416C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 416 | chr16 | 84479497 | ||||||
chr16:84479516 | G | A | 11 | a0001c0001t0039 a0001c0001t0091 a0001c0005t0129 others(8): Show |
16 | HG01175.hp2 HG02109.hp2 HG02280.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 397 | chr16 | 84479516 | ||||||
chr16:84479534 | C | T | 3 | a0001c0001t0147 a0001c0002t0146 a0001c0002t0148 |
3 | HG02040.hp2 HG02071.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 379 | chr16 | 84479534 | ||||||
chr16:84479535 | G | A | 4 | a0001c0001t0039 a0001c0001t0091 a0002c0003t0115 others(1): Show |
5 | HG01169.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*378C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 378 | chr16 | 84479535 | ||||||
chr16:84479542 | C | T | 1 | a0002c0003t0116 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*371G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 371 | chr16 | 84479542 | ||||||
chr16:84479554 | G | A | 13 | a0001c0005t0129 a0001c0005t0130 a0002c0003t0093 others(10): Show |
18 | HG00639.hp1 HG01169.hp2 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*359C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 359 | chr16 | 84479554 | ||||||
chr16:84479554 | G | GGAATTCC others(31): Show |
1 | a0004c0011t0094 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358_*359insTGCTGG others(32): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 358 | chr16 | 84479554 | ||||||
chr16:84479554 | G | GGAATTCC others(50): Show |
1 | a0004c0011t0095 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358_*359insTGCTGG others(51): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 358 | chr16 | 84479554 | ||||||
chr16:84479554 | G | GGAATTCC others(88): Show |
3 | a0003c0004t0052 a0003c0004t0138 a0015c0038t0052 |
3 | HG02723.hp2 HG03130.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*358_*359insTGCTGG others(89): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 358 | chr16 | 84479554 | ||||||
chr16:84479554 | G | GGAATTCC others(107): Show |
1 | a0004c0011t0096 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358_*359insTGCTGG others(108): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 358 | chr16 | 84479554 | ||||||
chr16:84479554 | G | GGAATTCC others(126): Show |
1 | a0002c0010t0040 | 2 | HG02145.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*358_*359insTGCTGG others(127): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 358 | chr16 | 84479554 | ||||||
chr16:84479554 | G | GGAATTCC others(145): Show |
1 | a0004c0011t0097 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358_*359insTGCTGG others(146): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 358 | chr16 | 84479554 | ||||||
chr16:84479611 | G | C | 1 | a0002c0003t0050 | 2 | HG01081.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*302C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 302 | chr16 | 84479611 | ||||||
chr16:84479635 | T | C | 5 | a0001c0005t0130 a0001c0005t0141 a0002c0016t0051 others(2): Show |
6 | HG00639.hp1 HG01884.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*278A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 278 | chr16 | 84479635 | ||||||
chr16:84479693 | A | C | 191 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(188): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
3_prime_UTR_variant | MODIFIER | c.*220T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 220 | chr16 | 84479693 | ||||||
chr16:84479727 | G | A | 1 | a0002c0003t0139 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 186 | chr16 | 84479727 | ||||||
chr16:84479750 | A | G | 33 | a0001c0001t0030 a0001c0001t0053 a0001c0001t0100 others(30): Show |
43 | HG01109.hp2 HG01169.hp2 HG01243.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*163T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 163 | chr16 | 84479750 | ||||||
chr16:84479771 | T | C | 4 | a0001c0001t0220 a0001c0005t0140 a0001c0005t0141 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*142A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 142 | chr16 | 84479771 | ||||||
chr16:84479791 | A | T | 103 | a0001c0001t0008 a0001c0001t0024 a0001c0001t0035 others(100): Show |
157 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*122T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 122 | chr16 | 84479791 | ||||||
chr16:84479803 | G | A | 1 | a0001c0001t0221 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 110 | chr16 | 84479803 | ||||||
chr16:84479806 | C | T | 1 | a0002c0003t0112 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 107 | chr16 | 84479806 | ||||||
chr16:84479812 | G | A | 1 | a0003c0004t0222 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 101 | chr16 | 84479812 | ||||||
chr16:84479857 | T | G | 196 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(193): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 56 | chr16 | 84479857 | ||||||
chr16:84479911 | C | T | 1 | a0001c0001t0070 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 8/8 | 2 | chr16 | 84479911 | ||||||
chr16:84504607 | G | C | 1 | a0001c0001t0223 | 1 | NA18612.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/8 | 6521 | chr16 | 84504607 | ||||||
chr16:84504626 | G | C | 6 | a0001c0001t0228 a0001c0006t0069 a0002c0009t0227 others(3): Show |
7 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/8 | 6540 | chr16 | 84504626 | ||||||
chr16:84504646 | G | C | 1 | a0001c0001t0229 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/8 | 6560 | chr16 | 84504646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:84480055 | T | A | 1 | a0002c0019t0027g0418 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1258-29A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480055 | |||||||
chr16:84480076 | G | A | 10 | a0002c0003t0093g0437 a0002c0010t0040g0010 a0002c0019t0027g0402 others(7): Show |
11 | HG02145.hp2 HG02258.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1258-50C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480076 | |||||||
chr16:84480122 | G | A | 1 | a0003c0004t0222g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1258-96C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480122 | |||||||
chr16:84480299 | C | T | 1 | a0001c0001t0228g0443 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1257+230G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480299 | |||||||
chr16:84480309 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1257+220C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480309 | |||||||
chr16:84480316 | C | G | 2 | a0001c0002t0171g0362 a0001c0002t0188g0363 |
2 | NA19068.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1257+213G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480316 | |||||||
chr16:84480329 | G | A | 1 | a0011c0024t0004g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1257+200C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480329 | |||||||
chr16:84480374 | G | C | 2 | a0002c0003t0135g0114 a0007c0012t0084g0113 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1257+155C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480374 | |||||||
chr16:84480413 | C | T | 1 | a0002c0019t0027g0418 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1257+116G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480413 | |||||||
chr16:84480455 | T | C | 70 | a0001c0001t0001g0267 a0001c0001t0001g0393 a0001c0001t0003g0029 others(67): Show |
70 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1257+74A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480455 | |||||||
chr16:84480460 | G | C | 2 | a0003c0004t0041g0427 a0003c0004t0041g0428 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1257+69C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480460 | |||||||
chr16:84480518 | G | C | 2 | a0001c0002t0056g0319 a0001c0002t0056g0320 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1257+11C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 7/7 | chr16 | 84480518 | |||||||
chr16:84480735 | A | G | 150 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(147): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1078-27T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84480735 | |||||||
chr16:84480797 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1078-89C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84480797 | |||||||
chr16:84481031 | G | A | 2 | a0001c0002t0056g0319 a0001c0002t0056g0320 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1078-323C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481031 | |||||||
chr16:84481033 | G | T | 6 | a0001c0001t0053g0434 a0001c0001t0053g0435 a0001c0001t0161g0110 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-325C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481033 | |||||||
chr16:84481047 | C | T | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1078-339G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481047 | |||||||
chr16:84481059 | AG | A | 142 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(139): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1078-352delC | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481059 | |||||||
chr16:84481069 | T | G | 2 | a0002c0003t0048g0003 a0002c0003t0123g0035 |
3 | HG03491.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1078-361A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481069 | |||||||
chr16:84481088 | T | C | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1078-380A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481088 | |||||||
chr16:84481099 | T | C | 1 | a0001c0001t0036g0116 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1078-391A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481099 | |||||||
chr16:84481146 | A | G | 2 | a0001c0001t0031g0086 a0001c0001t0031g0087 |
2 | NA18960.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1078-438T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481146 | |||||||
chr16:84481156 | G | A | 1 | a0002c0023t0196g0209 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1078-448C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481156 | |||||||
chr16:84481159 | A | T | 6 | a0001c0001t0100g0429 a0001c0001t0101g0187 a0001c0001t0102g0350 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-451T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481159 | |||||||
chr16:84481193 | G | T | 1 | a0001c0002t0001g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1078-485C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481193 | |||||||
chr16:84481224 | T | C | 1 | a0001c0001t0172g0038 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1078-516A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481224 | |||||||
chr16:84481282 | G | A | 1 | a0001c0005t0179g0403 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1078-574C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481282 | |||||||
chr16:84481312 | T | G | 442 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(439): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.1078-604A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481312 | |||||||
chr16:84481347 | AC | A | 11 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078-640delG | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481347 | |||||||
chr16:84481358 | G | A | 63 | a0001c0005t0072g0044 a0001c0005t0073g0094 a0001c0027t0029g0299 others(60): Show |
72 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1078-650C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481358 | |||||||
chr16:84481385 | G | C | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1078-677C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481385 | |||||||
chr16:84481413 | C | T | 1 | a0003c0004t0107g0436 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078-705G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481413 | |||||||
chr16:84481421 | G | A | 1 | a0001c0006t0113g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1078-713C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481421 | |||||||
chr16:84481521 | C | T | 1 | a0001c0001t0003g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1078-813G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481521 | |||||||
chr16:84481539 | G | A | 1 | a0001c0001t0031g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1078-831C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481539 | |||||||
chr16:84481562 | G | A | 1 | a0022c0039t0014g0142 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1078-854C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481562 | |||||||
chr16:84481569 | G | A | 1 | a0002c0003t0062g0378 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1078-861C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481569 | |||||||
chr16:84481611 | G | A | 1 | a0001c0002t0004g0310 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1078-903C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481611 | |||||||
chr16:84481636 | A | G | 30 | a0001c0001t0001g0055 a0001c0001t0001g0089 a0001c0001t0001g0099 others(27): Show |
31 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1078-928T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481636 | |||||||
chr16:84481740 | T | C | 15 | a0001c0002t0143g0326 a0002c0003t0093g0437 a0002c0019t0027g0402 others(12): Show |
15 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+852A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481740 | |||||||
chr16:84481760 | C | T | 1 | a0001c0001t0012g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1077+832G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481760 | |||||||
chr16:84481771 | A | G | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+821T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481771 | |||||||
chr16:84481772 | A | G | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+820T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481772 | |||||||
chr16:84481773 | A | G | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+819T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481773 | |||||||
chr16:84481774 | A | T | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+818T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481774 | |||||||
chr16:84481779 | A | C | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+813T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481779 | |||||||
chr16:84481780 | A | C | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+812T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481780 | |||||||
chr16:84481782 | A | T | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+810T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481782 | |||||||
chr16:84481784 | A | G | 1 | a0001c0002t0083g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+808T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481784 | |||||||
chr16:84481802 | C | T | 3 | a0001c0001t0030g0335 a0001c0001t0030g0336 a0001c0001t0030g0368 |
3 | HG02717.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1077+790G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481802 | |||||||
chr16:84481833 | C | G | 97 | a0001c0002t0001g0011 a0001c0002t0001g0020 a0001c0002t0001g0103 others(94): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1077+759G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481833 | |||||||
chr16:84481856 | C | A | 1 | a0001c0001t0006g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1077+736G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481856 | |||||||
chr16:84481876 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0002g0232 |
2 | NA19011.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1077+716C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481876 | |||||||
chr16:84481889 | G | A | 3 | a0001c0001t0030g0335 a0001c0001t0030g0336 a0001c0001t0030g0368 |
3 | HG02717.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1077+703C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481889 | |||||||
chr16:84481891 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1077+701C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481891 | |||||||
chr16:84481905 | G | T | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+687C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481905 | |||||||
chr16:84481912 | C | G | 61 | a0001c0005t0072g0044 a0001c0005t0073g0094 a0001c0027t0029g0299 others(58): Show |
69 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1077+680G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481912 | |||||||
chr16:84481964 | G | C | 61 | a0001c0005t0072g0044 a0001c0005t0073g0094 a0001c0027t0029g0299 others(58): Show |
70 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1077+628C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84481964 | |||||||
chr16:84482024 | G | A | 1 | a0019c0030t0109g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1077+568C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482024 | |||||||
chr16:84482067 | G | A | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1077+525C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482067 | |||||||
chr16:84482081 | C | T | 1 | a0002c0003t0127g0222 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1077+511G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482081 | |||||||
chr16:84482090 | G | A | 1 | a0001c0002t0059g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1077+502C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482090 | |||||||
chr16:84482101 | C | T | 63 | a0001c0005t0072g0044 a0001c0005t0073g0094 a0001c0027t0029g0299 others(60): Show |
72 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1077+491G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482101 | |||||||
chr16:84482106 | G | C | 308 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(305): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1077+486C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482106 | |||||||
chr16:84482132 | C | A | 2 | a0003c0004t0052g0340 a0003c0004t0138g0342 |
2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1077+460G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482132 | |||||||
chr16:84482146 | G | A | 1 | a0002c0013t0025g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1077+446C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482146 | |||||||
chr16:84482175 | A | C | 1 | a0002c0010t0133g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1077+417T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482175 | |||||||
chr16:84482176 | A | C | 23 | a0002c0003t0028g0023 a0002c0003t0042g0219 a0002c0013t0025g0018 others(20): Show |
23 | HG00735.hp1 HG01255.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.1077+416T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482176 | |||||||
chr16:84482207 | C | T | 1 | a0001c0001t0009g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1077+385G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482207 | |||||||
chr16:84482235 | C | T | 1 | a0001c0002t0056g0319 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1077+357G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482235 | |||||||
chr16:84482246 | G | A | 308 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(305): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1077+346C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482246 | |||||||
chr16:84482259 | G | A | 2 | a0001c0002t0001g0313 a0001c0005t0071g0407 |
2 | HG02165.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1077+333C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482259 | |||||||
chr16:84482268 | G | A | 3 | a0001c0005t0140g0432 a0001c0005t0141g0348 a0021c0031t0219g0112 |
3 | HG02559.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077+324C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482268 | |||||||
chr16:84482354 | T | C | 99 | a0001c0001t0045g0015 a0001c0002t0001g0011 a0001c0002t0001g0020 others(96): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1077+238A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482354 | |||||||
chr16:84482407 | G | A | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+185C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482407 | |||||||
chr16:84482424 | G | A | 3 | a0001c0005t0140g0432 a0001c0005t0141g0348 a0021c0031t0219g0112 |
3 | HG02559.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077+168C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482424 | |||||||
chr16:84482450 | A | C | 1 | a0001c0001t0119g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1077+142T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482450 | |||||||
chr16:84482473 | G | A | 11 | a0001c0005t0140g0432 a0001c0005t0141g0348 a0002c0009t0020g0382 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1077+119C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482473 | |||||||
chr16:84482484 | A | G | 442 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(439): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.1077+108T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 6/7 | chr16 | 84482484 | |||||||
chr16:84482789 | C | A | 1 | a0001c0001t0011g0258 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.959-79G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84482789 | |||||||
chr16:84482913 | G | A | 14 | a0002c0003t0047g0376 a0002c0003t0047g0377 a0002c0003t0062g0378 others(11): Show |
15 | HG00099.hp1 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.959-203C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84482913 | |||||||
chr16:84482957 | G | T | 3 | a0001c0005t0071g0407 a0001c0005t0129g0413 a0001c0005t0130g0431 |
3 | HG03225.hp1 NA18522.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.959-247C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84482957 | |||||||
chr16:84482992 | G | T | 13 | a0002c0003t0047g0376 a0002c0003t0047g0377 a0002c0003t0062g0378 others(10): Show |
14 | HG00099.hp1 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.959-282C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84482992 | |||||||
chr16:84483150 | G | A | 1 | a0001c0001t0011g0349 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.959-440C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483150 | |||||||
chr16:84483253 | A | C | 1 | a0001c0017t0022g0200 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.959-543T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483253 | |||||||
chr16:84483297 | T | A | 1 | a0001c0017t0022g0200 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.959-587A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483297 | |||||||
chr16:84483344 | C | G | 1 | a0001c0001t0013g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.959-634G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483344 | |||||||
chr16:84483358 | G | A | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.959-648C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483358 | |||||||
chr16:84483371 | C | T | 4 | a0001c0001t0003g0024 a0001c0001t0003g0046 a0001c0001t0003g0052 others(1): Show |
4 | HG00544.hp1 HG00558.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-661G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483371 | |||||||
chr16:84483422 | G | C | 3 | a0001c0005t0140g0432 a0001c0005t0141g0348 a0021c0031t0219g0112 |
3 | HG02559.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.959-712C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483422 | |||||||
chr16:84483425 | C | T | 1 | a0001c0001t0024g0135 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.959-715G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483425 | |||||||
chr16:84483532 | G | A | 2 | a0002c0003t0028g0023 a0002c0003t0042g0219 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.959-822C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483532 | |||||||
chr16:84483657 | G | A | 212 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(209): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.959-947C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483657 | |||||||
chr16:84483674 | G | C | 1 | a0001c0017t0022g0200 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.959-964C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483674 | |||||||
chr16:84483682 | C | T | 61 | a0001c0001t0022g0169 a0001c0005t0073g0094 a0001c0027t0029g0299 others(58): Show |
70 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.959-972G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483682 | |||||||
chr16:84483705 | G | T | 1 | a0001c0017t0022g0200 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.959-995C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483705 | |||||||
chr16:84483740 | G | C | 2 | a0002c0003t0048g0003 a0002c0003t0123g0035 |
3 | HG03491.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.959-1030C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483740 | |||||||
chr16:84483741 | A | G | 1 | a0001c0001t0031g0170 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.959-1031T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483741 | |||||||
chr16:84483781 | C | G | 5 | a0002c0003t0007g0190 a0002c0003t0010g0189 a0002c0003t0050g0009 others(2): Show |
6 | HG01081.hp1 HG01106.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.959-1071G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483781 | |||||||
chr16:84483828 | G | A | 11 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.959-1118C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483828 | |||||||
chr16:84483840 | G | A | 2 | a0002c0003t0007g0075 a0002c0003t0010g0071 |
2 | NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.959-1130C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483840 | |||||||
chr16:84483965 | G | T | 1 | a0001c0001t0208g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.959-1255C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483965 | |||||||
chr16:84483999 | T | C | 1 | a0001c0001t0003g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.959-1289A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84483999 | |||||||
chr16:84484038 | C | T | 212 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(209): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.959-1328G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484038 | |||||||
chr16:84484041 | C | T | 11 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.959-1331G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484041 | |||||||
chr16:84484043 | C | G | 1 | a0002c0010t0133g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.959-1333G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484043 | |||||||
chr16:84484062 | C | A | 1 | a0001c0001t0100g0429 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.959-1352G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484062 | |||||||
chr16:84484081 | C | A | 1 | a0001c0002t0066g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.959-1371G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484081 | |||||||
chr16:84484114 | G | A | 212 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(209): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.959-1404C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484114 | |||||||
chr16:84484120 | C | G | 1 | a0002c0010t0133g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.959-1410G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484120 | |||||||
chr16:84484156 | C | T | 1 | a0009c0037t0114g0386 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.959-1446G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484156 | |||||||
chr16:84484182 | C | A | 1 | a0002c0003t0115g0438 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.959-1472G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484182 | |||||||
chr16:84484234 | A | G | 215 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(212): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.959-1524T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484234 | |||||||
chr16:84484247 | G | C | 9 | a0002c0003t0093g0437 a0002c0019t0027g0402 a0002c0019t0027g0418 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.959-1537C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484247 | |||||||
chr16:84484264 | T | C | 3 | a0001c0001t0006g0213 a0001c0001t0086g0214 a0001c0001t0087g0212 |
3 | HG00639.hp2 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.959-1554A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484264 | |||||||
chr16:84484363 | G | A | 6 | a0001c0001t0100g0429 a0001c0001t0101g0187 a0001c0001t0102g0350 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.959-1653C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484363 | |||||||
chr16:84484559 | C | A | 1 | a0001c0001t0055g0173 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.959-1849G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484559 | |||||||
chr16:84484560 | C | A | 59 | a0001c0027t0029g0299 a0002c0003t0001g0122 a0002c0003t0001g0154 others(56): Show |
68 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.959-1850G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484560 | |||||||
chr16:84484731 | C | T | 1 | a0002c0003t0120g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.958+1900G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484731 | |||||||
chr16:84484733 | T | C | 5 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.958+1898A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484733 | |||||||
chr16:84484801 | G | A | 1 | a0001c0002t0176g0311 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.958+1830C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484801 | |||||||
chr16:84484832 | G | A | 1 | a0015c0038t0052g0343 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.958+1799C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484832 | |||||||
chr16:84484857 | G | C | 1 | a0004c0011t0096g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.958+1774C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484857 | |||||||
chr16:84484919 | G | C | 1 | a0002c0013t0085g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.958+1712C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484919 | |||||||
chr16:84484973 | T | G | 1 | a0013c0033t0106g0373 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.958+1658A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84484973 | |||||||
chr16:84485043 | G | T | 1 | a0003c0004t0018g0411 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.958+1588C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485043 | |||||||
chr16:84485046 | C | A | 61 | a0001c0027t0029g0299 a0002c0003t0001g0122 a0002c0003t0001g0154 others(58): Show |
70 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.958+1585G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485046 | |||||||
chr16:84485088 | G | A | 4 | a0001c0002t0143g0326 a0004c0020t0121g0032 a0004c0020t0142g0409 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+1543C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485088 | |||||||
chr16:84485128 | G | A | 1 | a0001c0001t0009g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.958+1503C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485128 | |||||||
chr16:84485128 | G | C | 1 | a0012c0032t0019g0036 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.958+1503C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485128 | |||||||
chr16:84485138 | G | A | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.958+1493C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485138 | |||||||
chr16:84485173 | G | A | 1 | a0001c0002t0001g0020 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.958+1458C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485173 | |||||||
chr16:84485206 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.958+1425G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485206 | |||||||
chr16:84485348 | A | G | 206 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(203): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.958+1283T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485348 | |||||||
chr16:84485369 | A | G | 76 | a0001c0001t0001g0037 a0001c0001t0001g0083 a0001c0001t0001g0267 others(73): Show |
80 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.958+1262T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485369 | |||||||
chr16:84485433 | G | A | 1 | a0001c0001t0208g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.958+1198C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485433 | |||||||
chr16:84485439 | G | A | 6 | a0001c0005t0071g0407 a0001c0005t0129g0413 a0001c0005t0130g0431 others(3): Show |
6 | HG02559.hp2 HG03225.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.958+1192C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485439 | |||||||
chr16:84485476 | C | T | 1 | a0001c0002t0177g0361 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.958+1155G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485476 | |||||||
chr16:84485587 | G | A | 1 | a0009c0037t0114g0386 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.958+1044C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485587 | |||||||
chr16:84485629 | A | ACTAT | 3 | a0001c0001t0003g0024 a0006c0007t0008g0012 a0006c0007t0008g0351 |
4 | HG00558.hp2 NA18954.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+998_958+1001du others(5): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485629 | |||||||
chr16:84485639 | T | TATCTATC others(1): Show |
210 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(207): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.958+991_958+992ins others(8): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485639 | |||||||
chr16:84485639 | TATCC | T | 61 | a0001c0027t0029g0299 a0002c0003t0001g0122 a0002c0003t0001g0154 others(58): Show |
70 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.958+988_958+991del others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485639 | |||||||
chr16:84485643 | C | T | 1 | a0001c0001t0001g0364 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.958+988G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485643 | |||||||
chr16:84485663 | C | T | 1 | a0002c0003t0145g0191 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.958+968G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485663 | |||||||
chr16:84485669 | T | C | 211 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(208): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.958+962A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485669 | |||||||
chr16:84485673 | C | CCTAT | 90 | a0001c0001t0045g0015 a0001c0002t0001g0011 a0001c0002t0001g0020 others(87): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.958+954_958+957dup others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485673 | C | CCTATCTA others(1): Show |
12 | a0001c0002t0001g0179 a0001c0002t0002g0027 a0001c0002t0034g0175 others(9): Show |
13 | HG00438.hp2 HG01099.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.958+950_958+957dup others(8): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485673 | C | CCTATCTA others(5): Show |
40 | a0002c0003t0001g0122 a0002c0003t0006g0131 a0002c0003t0007g0006 others(37): Show |
46 | HG00423.hp2 HG00733.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.958+946_958+957dup others(12): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485673 | C | CCTATCTA others(9): Show |
15 | a0001c0027t0029g0299 a0002c0003t0007g0096 a0002c0003t0007g0097 others(12): Show |
17 | HG00673.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.958+942_958+957dup others(16): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485673 | C | CCTATCTA others(13): Show |
1 | a0002c0003t0139g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.958+938_958+957dup others(20): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485673 | C | T | 1 | a0002c0003t0145g0191 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.958+958G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485673 | CCTAT | C | 5 | a0001c0002t0001g0315 a0001c0002t0004g0098 a0001c0002t0004g0316 others(2): Show |
5 | NA18960.hp1 NA18962.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.958+954_958+957del others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485673 | |||||||
chr16:84485677 | T | C | 214 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(211): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.958+954A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485677 | |||||||
chr16:84485681 | T | C | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.958+950A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485681 | |||||||
chr16:84485686 | C | T | 211 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(208): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.958+945G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485686 | |||||||
chr16:84485738 | G | A | 1 | a0001c0002t0001g0274 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.958+893C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485738 | |||||||
chr16:84485774 | G | C | 214 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.958+857C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485774 | |||||||
chr16:84485827 | A | G | 442 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(439): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.958+804T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485827 | |||||||
chr16:84485831 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.958+800C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485831 | |||||||
chr16:84485883 | C | G | 210 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(207): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.958+748G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485883 | |||||||
chr16:84485933 | C | T | 2 | a0001c0006t0043g0215 a0001c0006t0043g0331 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.958+698G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485933 | |||||||
chr16:84485987 | A | AT | 13 | a0001c0002t0143g0326 a0002c0003t0115g0438 a0002c0003t0135g0114 others(10): Show |
13 | HG01169.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.958+643dupA | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485987 | |||||||
chr16:84485987 | A | T | 2 | a0003c0004t0041g0427 a0003c0004t0041g0428 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.958+644T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485987 | |||||||
chr16:84485987 | AT | A | 65 | a0001c0027t0029g0299 a0002c0003t0001g0122 a0002c0003t0001g0154 others(62): Show |
74 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.958+643delA | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485987 | |||||||
chr16:84485989 | T | TA | 325 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(322): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.958+641_958+642ins others(1): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485989 | |||||||
chr16:84485990 | T | A | 11 | a0001c0001t0147g0229 a0001c0002t0006g0277 a0002c0003t0093g0437 others(8): Show |
11 | HG02040.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.958+641A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485990 | |||||||
chr16:84485992 | T | A | 215 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(212): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.958+639A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485992 | |||||||
chr16:84485993 | T | A | 1 | a0001c0001t0147g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.958+638A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485993 | |||||||
chr16:84485995 | T | A | 16 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0008g0013 others(13): Show |
18 | HG00408.hp1 HG00735.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.958+636A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84485995 | |||||||
chr16:84486124 | C | G | 1 | a0009c0037t0114g0386 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.958+507G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486124 | |||||||
chr16:84486157 | C | T | 1 | a0002c0003t0136g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.958+474G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486157 | |||||||
chr16:84486229 | T | TG | 4 | a0001c0002t0143g0326 a0004c0020t0121g0032 a0004c0020t0142g0409 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+401dupC | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486229 | |||||||
chr16:84486267 | C | T | 5 | a0002c0003t0135g0114 a0007c0012t0037g0332 a0007c0012t0037g0367 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.958+364G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486267 | |||||||
chr16:84486270 | TG | T | 217 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(214): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.958+360delC | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486270 | |||||||
chr16:84486276 | C | T | 217 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(214): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.958+355G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486276 | |||||||
chr16:84486284 | G | C | 9 | a0002c0003t0093g0437 a0002c0019t0027g0402 a0002c0019t0027g0418 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.958+347C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486284 | |||||||
chr16:84486411 | T | C | 108 | a0001c0001t0045g0015 a0001c0002t0001g0011 a0001c0002t0001g0020 others(105): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.958+220A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486411 | |||||||
chr16:84486416 | G | A | 339 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(336): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.958+215C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486416 | |||||||
chr16:84486474 | T | C | 323 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(320): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.958+157A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486474 | |||||||
chr16:84486501 | C | T | 1 | a0001c0001t0198g0396 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.958+130G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486501 | |||||||
chr16:84486567 | C | T | 9 | a0002c0003t0047g0376 a0002c0003t0047g0377 a0002c0003t0062g0378 others(6): Show |
10 | HG00099.hp1 HG01255.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.958+64G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486567 | |||||||
chr16:84486617 | A | T | 323 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(320): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.958+14T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 5/7 | chr16 | 84486617 | |||||||
chr16:84487065 | G | A | 4 | a0002c0010t0040g0010 a0002c0010t0044g0346 a0002c0010t0132g0205 others(1): Show |
5 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.530-6C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487065 | |||||||
chr16:84487174 | G | C | 442 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(439): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.530-115C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487174 | |||||||
chr16:84487297 | A | C | 1 | a0002c0003t0115g0438 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.530-238T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487297 | |||||||
chr16:84487333 | CCT | C | 68 | a0001c0027t0029g0299 a0002c0003t0001g0122 a0002c0003t0001g0154 others(65): Show |
77 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.530-276_530-275del others(2): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487333 | |||||||
chr16:84487373 | G | T | 99 | a0001c0002t0001g0011 a0001c0002t0001g0020 a0001c0002t0001g0103 others(96): Show |
100 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.530-314C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487373 | |||||||
chr16:84487410 | A | G | 1 | a0001c0001t0144g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.530-351T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487410 | |||||||
chr16:84487430 | G | A | 9 | a0002c0003t0093g0437 a0002c0019t0027g0402 a0002c0019t0027g0418 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-371C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487430 | |||||||
chr16:84487507 | G | C | 319 | a0001c0001t0001g0055 a0001c0001t0001g0089 a0001c0001t0001g0099 others(316): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.530-448C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487507 | |||||||
chr16:84487665 | A | C | 1 | a0002c0003t0127g0222 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.530-606T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487665 | |||||||
chr16:84487763 | C | A | 5 | a0002c0003t0007g0190 a0002c0003t0010g0189 a0002c0003t0050g0009 others(2): Show |
6 | HG01081.hp1 HG01106.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.530-704G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487763 | |||||||
chr16:84487766 | G | C | 329 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(326): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.530-707C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487766 | |||||||
chr16:84487791 | C | G | 2 | a0002c0003t0048g0003 a0002c0003t0123g0035 |
3 | HG03491.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.530-732G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487791 | |||||||
chr16:84487847 | A | G | 324 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(321): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.530-788T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487847 | |||||||
chr16:84487881 | C | T | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530-822G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487881 | |||||||
chr16:84487972 | G | A | 324 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(321): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.530-913C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84487972 | |||||||
chr16:84488046 | C | T | 58 | a0001c0001t0001g0267 a0001c0001t0001g0393 a0001c0001t0006g0392 others(55): Show |
58 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.530-987G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488046 | |||||||
chr16:84488090 | CA | C | 3 | a0001c0005t0140g0432 a0001c0005t0141g0348 a0021c0031t0219g0112 |
3 | HG02559.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.530-1032delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488090 | |||||||
chr16:84488222 | G | A | 324 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(321): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.529+1056C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488222 | |||||||
chr16:84488237 | A | C | 324 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(321): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.529+1041T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488237 | |||||||
chr16:84488256 | G | A | 1 | a0002c0003t0007g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.529+1022C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488256 | |||||||
chr16:84488273 | T | C | 104 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(101): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.529+1005A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488273 | |||||||
chr16:84488307 | C | T | 2 | a0005c0008t0090g0204 a0005c0008t0098g0338 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.529+971G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488307 | |||||||
chr16:84488343 | T | C | 105 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(102): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.529+935A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488343 | |||||||
chr16:84488346 | A | C | 1 | a0001c0001t0005g0243 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.529+932T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488346 | |||||||
chr16:84488350 | T | A | 11 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+928A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488350 | |||||||
chr16:84488424 | GT | G | 72 | a0002c0003t0001g0122 a0002c0003t0001g0154 a0002c0003t0006g0131 others(69): Show |
81 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.529+853delA | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488424 | |||||||
chr16:84488457 | T | C | 1 | a0001c0002t0153g0321 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.529+821A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488457 | |||||||
chr16:84488588 | T | C | 215 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(212): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.529+690A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488588 | |||||||
chr16:84488653 | C | T | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.529+625G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488653 | |||||||
chr16:84488690 | C | T | 103 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(100): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.529+588G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488690 | |||||||
chr16:84488694 | T | C | 1 | a0001c0001t0016g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.529+584A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488694 | |||||||
chr16:84488718 | G | T | 4 | a0001c0002t0143g0326 a0004c0020t0121g0032 a0004c0020t0142g0409 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+560C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488718 | |||||||
chr16:84488726 | G | T | 2 | a0001c0006t0043g0215 a0001c0006t0043g0331 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.529+552C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488726 | |||||||
chr16:84488836 | G | C | 2 | a0003c0004t0041g0427 a0003c0004t0041g0428 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.529+442C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488836 | |||||||
chr16:84488845 | G | A | 1 | a0001c0001t0017g0166 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.529+433C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488845 | |||||||
chr16:84488919 | A | G | 103 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(100): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.529+359T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84488919 | |||||||
chr16:84489001 | A | T | 209 | a0001c0001t0001g0055 a0001c0001t0001g0089 a0001c0001t0001g0099 others(206): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.529+277T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489001 | |||||||
chr16:84489003 | T | C | 442 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(439): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.529+275A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489003 | |||||||
chr16:84489016 | G | A | 60 | a0001c0001t0001g0267 a0001c0001t0001g0393 a0001c0001t0003g0029 others(57): Show |
60 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.529+262C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489016 | |||||||
chr16:84489060 | C | G | 323 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(320): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.529+218G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489060 | |||||||
chr16:84489088 | G | A | 2 | a0001c0001t0009g0158 a0001c0001t0009g0159 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.529+190C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489088 | |||||||
chr16:84489096 | C | CCT | 3 | a0004c0020t0121g0032 a0004c0020t0142g0409 a0015c0038t0052g0343 |
3 | HG02615.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.529+180_529+181dup others(2): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489096 | |||||||
chr16:84489198 | A | G | 1 | a0001c0001t0013g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.529+80T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489198 | |||||||
chr16:84489261 | C | A | 322 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(319): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.529+17G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 4/7 | chr16 | 84489261 | |||||||
chr16:84489425 | G | T | 12 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.385-3C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84489425 | |||||||
chr16:84489478 | G | A | 103 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(100): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.385-56C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84489478 | |||||||
chr16:84489546 | G | C | 2 | a0012c0032t0019g0036 a0022c0039t0014g0142 |
2 | HG00733.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.385-124C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84489546 | |||||||
chr16:84489729 | G | T | 2 | a0006c0007t0026g0101 a0006c0007t0026g0102 |
2 | NA18944.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.385-307C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84489729 | |||||||
chr16:84489794 | G | T | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385-372C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84489794 | |||||||
chr16:84489986 | A | G | 394 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(391): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.385-564T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84489986 | |||||||
chr16:84490016 | C | T | 1 | a0001c0001t0070g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.385-594G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490016 | |||||||
chr16:84490043 | T | C | 1 | a0007c0012t0076g0345 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385-621A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490043 | |||||||
chr16:84490111 | C | T | 1 | a0001c0001t0077g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.385-689G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490111 | |||||||
chr16:84490184 | T | G | 227 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(224): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.385-762A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490184 | |||||||
chr16:84490207 | G | C | 4 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-785C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490207 | |||||||
chr16:84490235 | T | C | 1 | a0001c0001t0013g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.385-813A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490235 | |||||||
chr16:84490280 | G | GA | 74 | a0001c0001t0001g0055 a0001c0001t0001g0393 a0001c0027t0029g0299 others(71): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.385-859dupT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490280 | |||||||
chr16:84490280 | GA | G | 11 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-859delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490280 | |||||||
chr16:84490281 | A | C | 5 | a0005c0008t0079g0030 a0005c0008t0080g0031 a0005c0008t0088g0188 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-859T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490281 | |||||||
chr16:84490321 | G | T | 1 | a0002c0003t0136g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-899C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490321 | |||||||
chr16:84490321 | GA | G | 13 | a0001c0001t0001g0240 a0001c0001t0001g0275 a0001c0001t0002g0232 others(10): Show |
14 | HG00558.hp1 HG02074.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.385-900delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490321 | |||||||
chr16:84490348 | G | A | 1 | a0001c0006t0113g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385-926C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490348 | |||||||
chr16:84490443 | C | CT | 7 | a0001c0005t0071g0407 a0002c0003t0028g0023 a0002c0003t0042g0219 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-1022dupA | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | C | CTT | 8 | a0003c0004t0018g0337 a0003c0004t0042g0423 a0003c0004t0107g0436 others(5): Show |
8 | HG00735.hp1 HG01358.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-1023_385-1022d others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTT | C | 17 | a0001c0001t0002g0108 a0001c0001t0003g0043 a0001c0001t0004g0081 others(14): Show |
17 | HG00621.hp2 HG00639.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-1025_385-1022d others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTT | C | 104 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(101): Show |
105 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.385-1026_385-1022d others(7): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTT | C | 101 | a0001c0001t0001g0099 a0001c0001t0001g0267 a0001c0001t0001g0275 others(98): Show |
108 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.385-1027_385-1022d others(8): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT | C | 34 | a0001c0001t0004g0305 a0001c0002t0001g0020 a0001c0002t0001g0140 others(31): Show |
34 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.385-1028_385-1022d others(9): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(1): Show |
C | 60 | a0001c0002t0001g0011 a0001c0002t0001g0103 a0001c0002t0001g0139 others(57): Show |
61 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.385-1029_385-1022d others(10): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(2): Show |
C | 12 | a0001c0002t0004g0404 a0001c0006t0043g0215 a0001c0006t0043g0331 others(9): Show |
12 | HG01256.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.385-1030_385-1022d others(11): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0001g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.385-1033_385-1022d others(14): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(7): Show |
C | 3 | a0003c0004t0018g0033 a0003c0004t0018g0410 a0003c0004t0225g0448 |
3 | HG01433.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.385-1035_385-1022d others(16): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(9): Show |
C | 3 | a0002c0003t0093g0437 a0002c0003t0115g0438 a0002c0003t0124g0123 |
3 | HG01123.hp1 HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.385-1037_385-1022d others(18): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(10): Show |
C | 3 | a0002c0003t0001g0122 a0002c0003t0015g0132 a0002c0003t0062g0146 |
3 | HG02738.hp1 HG04184.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.385-1038_385-1022d others(19): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490443 | CTTTTTTT others(11): Show |
C | 69 | a0002c0003t0001g0154 a0002c0003t0006g0131 a0002c0003t0007g0006 others(66): Show |
78 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.385-1039_385-1022d others(20): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490443 | |||||||
chr16:84490460 | T | C | 1 | a0002c0003t0124g0123 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.385-1038A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490460 | |||||||
chr16:84490461 | T | C | 3 | a0002c0003t0001g0122 a0002c0003t0015g0132 a0002c0003t0062g0146 |
3 | HG02738.hp1 HG04184.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.385-1039A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490461 | |||||||
chr16:84490462 | T | C | 62 | a0002c0003t0001g0154 a0002c0003t0006g0131 a0002c0003t0007g0006 others(59): Show |
71 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.385-1040A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490462 | |||||||
chr16:84490489 | G | A | 217 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(214): Show |
224 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.385-1067C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490489 | |||||||
chr16:84490621 | G | C | 218 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(215): Show |
226 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.385-1199C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490621 | |||||||
chr16:84490653 | G | GGT | 6 | a0001c0001t0022g0172 a0001c0001t0174g0399 a0001c0001t0178g0286 others(3): Show |
6 | HG00544.hp2 HG00621.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGT | 47 | a0001c0001t0001g0037 a0001c0001t0001g0083 a0001c0001t0001g0267 others(44): Show |
50 | HG01099.hp1 HG01175.hp1 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGT | 8 | a0001c0001t0013g0160 a0001c0001t0021g0167 a0001c0001t0021g0168 others(5): Show |
8 | HG03453.hp1 HG03540.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(8): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(1): Show |
14 | a0001c0001t0017g0166 a0001c0001t0021g0165 a0001c0001t0057g0197 others(11): Show |
14 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(10): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(3): Show |
22 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0240 others(19): Show |
23 | HG00408.hp1 HG00597.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(12): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(5): Show |
32 | a0001c0001t0001g0055 a0001c0001t0002g0232 a0001c0001t0002g0365 others(29): Show |
33 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(14): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(7): Show |
28 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0048 others(25): Show |
30 | HG00544.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(16): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(9): Show |
21 | a0001c0001t0003g0024 a0001c0001t0004g0236 a0001c0001t0005g0025 others(18): Show |
21 | HG00558.hp2 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(18): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(11): Show |
16 | a0001c0001t0005g0058 a0001c0001t0005g0062 a0001c0001t0006g0213 others(13): Show |
16 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(20): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(13): Show |
9 | a0001c0001t0005g0060 a0001c0001t0005g0253 a0001c0001t0013g0144 others(6): Show |
9 | HG00323.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(22): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(15): Show |
7 | a0001c0001t0003g0244 a0001c0001t0013g0255 a0001c0001t0035g0206 others(4): Show |
7 | HG01169.hp1 HG01496.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-1232_385-1231i others(24): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GGTGTGTG others(17): Show |
3 | a0001c0001t0003g0043 a0001c0001t0013g0254 a0015c0038t0052g0343 |
3 | HG00621.hp2 HG01168.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.385-1232_385-1231i others(26): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0199g0151 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.385-1232_385-1231i others(13): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GTGTGTGT others(8): Show |
1 | a0001c0005t0003g0358 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.385-1232_385-1231i others(17): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | G | GTGTGTGT others(10): Show |
1 | a0001c0001t0134g0329 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.385-1232_385-1231i others(19): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | GAT | G | 3 | a0001c0001t0045g0015 a0001c0001t0086g0214 a0004c0011t0095g0372 |
4 | HG01106.hp2 NA18953.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-1233_385-1232d others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490653 | GATGTGTG others(5): Show |
G | 1 | a0001c0001t0046g0093 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.385-1243_385-1232d others(14): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490653 | |||||||
chr16:84490654 | A | ATG | 86 | a0001c0001t0004g0305 a0001c0002t0001g0020 a0001c0002t0001g0137 others(83): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.385-1234_385-1233d others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTG | 15 | a0001c0002t0004g0298 a0001c0002t0214g0290 a0001c0006t0113g0328 others(12): Show |
17 | HG00140.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-1236_385-1233d others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTG | 20 | a0001c0002t0001g0297 a0001c0002t0004g0295 a0001c0002t0006g0143 others(17): Show |
21 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.385-1238_385-1233d others(8): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(1): Show |
7 | a0001c0002t0002g0293 a0001c0005t0149g0294 a0001c0006t0137g0421 others(4): Show |
7 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-1240_385-1233d others(10): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(3): Show |
3 | a0001c0002t0195g0292 a0001c0006t0043g0215 a0001c0006t0043g0331 |
3 | HG02027.hp1 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.385-1242_385-1233d others(12): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(7): Show |
1 | a0001c0002t0169g0291 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.385-1246_385-1233d others(16): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(9): Show |
1 | a0002c0016t0051g0216 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.385-1248_385-1233d others(18): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(11): Show |
2 | a0002c0009t0020g0385 a0002c0009t0020g0425 |
2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.385-1250_385-1233d others(20): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(13): Show |
2 | a0002c0009t0218g0384 a0002c0013t0025g0105 |
2 | HG01175.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.385-1252_385-1233d others(22): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(15): Show |
3 | a0002c0009t0020g0383 a0002c0009t0227g0444 a0014c0025t0224g0447 |
3 | HG02280.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.385-1254_385-1233d others(24): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(17): Show |
3 | a0002c0009t0020g0382 a0002c0013t0025g0018 a0002c0013t0085g0194 |
3 | HG02258.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.385-1256_385-1233d others(26): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | ATGTGTGT others(19): Show |
1 | a0002c0013t0025g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.385-1258_385-1233d others(28): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | A | G | 218 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(215): Show |
225 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.385-1232T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | ATG | A | 10 | a0001c0002t0001g0313 a0002c0003t0028g0023 a0002c0003t0029g0078 others(7): Show |
11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-1234_385-1233d others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | ATGTG | A | 4 | a0005c0008t0079g0030 a0005c0008t0080g0031 a0005c0008t0090g0204 others(1): Show |
4 | HG01884.hp1 HG02886.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1236_385-1233d others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | ATGTGTGT others(1): Show |
A | 18 | a0001c0002t0001g0139 a0003c0004t0018g0033 a0003c0004t0018g0337 others(15): Show |
18 | HG00735.hp1 HG01255.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-1240_385-1233d others(10): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490654 | ATGTGTGT others(3): Show |
A | 28 | a0001c0002t0001g0011 a0001c0002t0001g0140 a0001c0002t0001g0141 others(25): Show |
29 | HG00438.hp2 HG00609.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.385-1242_385-1233d others(12): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490654 | |||||||
chr16:84490717 | T | G | 1 | a0001c0001t0036g0136 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.385-1295A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490717 | |||||||
chr16:84490722 | T | C | 223 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(220): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.385-1300A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490722 | |||||||
chr16:84490863 | G | C | 8 | a0001c0001t0119g0042 a0001c0006t0043g0215 a0001c0006t0043g0331 others(5): Show |
8 | HG02523.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-1441C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490863 | |||||||
chr16:84490902 | A | G | 1 | a0015c0038t0052g0343 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385-1480T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490902 | |||||||
chr16:84490939 | C | G | 5 | a0004c0011t0092g0366 a0004c0011t0094g0370 a0004c0011t0095g0372 others(2): Show |
5 | HG02630.hp2 HG02970.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-1517G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490939 | |||||||
chr16:84490954 | G | C | 1 | a0003c0004t0018g0411 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385-1532C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490954 | |||||||
chr16:84490978 | C | CTGCT | 298 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(295): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.385-1560_385-1557d others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490978 | |||||||
chr16:84490987 | T | C | 4 | a0002c0010t0040g0010 a0002c0010t0044g0346 a0002c0010t0132g0205 others(1): Show |
5 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-1565A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84490987 | |||||||
chr16:84491008 | T | A | 16 | a0002c0003t0135g0114 a0002c0009t0020g0382 a0002c0009t0020g0383 others(13): Show |
16 | HG01175.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.385-1586A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491008 | |||||||
chr16:84491055 | T | G | 1 | a0001c0002t0188g0363 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.385-1633A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491055 | |||||||
chr16:84491063 | T | A | 7 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-1641A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491063 | |||||||
chr16:84491175 | C | A | 7 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-1753G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491175 | |||||||
chr16:84491177 | C | T | 1 | a0003c0004t0052g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385-1755G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491177 | |||||||
chr16:84491186 | T | C | 227 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(224): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.385-1764A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491186 | |||||||
chr16:84491191 | C | A | 96 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(93): Show |
97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.385-1769G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491191 | |||||||
chr16:84491210 | C | T | 2 | a0003c0004t0041g0427 a0003c0004t0041g0428 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.385-1788G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491210 | |||||||
chr16:84491211 | G | A | 1 | a0003c0004t0222g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.385-1789C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491211 | |||||||
chr16:84491311 | G | T | 214 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.385-1889C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491311 | |||||||
chr16:84491312 | C | T | 214 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.385-1890G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491312 | |||||||
chr16:84491341 | C | A | 7 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-1919G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491341 | |||||||
chr16:84491359 | G | T | 1 | a0007c0012t0037g0332 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.385-1937C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491359 | |||||||
chr16:84491367 | C | A | 220 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(217): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.385-1945G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491367 | |||||||
chr16:84491399 | T | C | 220 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(217): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.385-1977A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491399 | |||||||
chr16:84491404 | T | G | 220 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(217): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.385-1982A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491404 | |||||||
chr16:84491407 | C | A | 220 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(217): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.385-1985G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491407 | |||||||
chr16:84491408 | A | G | 220 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(217): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.385-1986T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491408 | |||||||
chr16:84491413 | C | T | 11 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(8): Show |
11 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-1991G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491413 | |||||||
chr16:84491479 | T | C | 413 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(410): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.385-2057A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491479 | |||||||
chr16:84491491 | G | A | 5 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-2069C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491491 | |||||||
chr16:84491511 | A | C | 294 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(291): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.385-2089T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491511 | |||||||
chr16:84491538 | T | TAAAAA | 170 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0099 others(167): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.385-2121_385-2117d others(7): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491538 | |||||||
chr16:84491538 | T | TAAAAAA | 43 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0240 others(40): Show |
43 | HG00741.hp1 HG01106.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.385-2122_385-2117d others(8): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491538 | |||||||
chr16:84491538 | TA | T | 21 | a0001c0002t0066g0202 a0001c0002t0083g0193 a0001c0002t0152g0318 others(18): Show |
21 | HG00639.hp1 HG01081.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.385-2117delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491538 | |||||||
chr16:84491538 | TAA | T | 196 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(193): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.385-2118_385-2117d others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491538 | |||||||
chr16:84491540 | A | T | 3 | a0001c0002t0066g0202 a0001c0002t0083g0193 a0001c0002t0152g0318 |
3 | NA18964.hp2 NA18997.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.385-2118T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491540 | |||||||
chr16:84491541 | A | T | 94 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(91): Show |
95 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.385-2119T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491541 | |||||||
chr16:84491588 | C | G | 1 | a0001c0001t0067g0394 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.385-2166G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491588 | |||||||
chr16:84491599 | G | A | 1 | a0004c0011t0096g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385-2177C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491599 | |||||||
chr16:84491605 | G | A | 96 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(93): Show |
97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.385-2183C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491605 | |||||||
chr16:84491612 | G | A | 62 | a0002c0003t0001g0122 a0002c0003t0001g0154 a0002c0003t0006g0131 others(59): Show |
71 | HG00099.hp1 HG00423.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.385-2190C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491612 | |||||||
chr16:84491620 | C | G | 97 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(94): Show |
98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.385-2198G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491620 | |||||||
chr16:84491641 | A | T | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.385-2219T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491641 | |||||||
chr16:84491699 | G | A | 1 | a0001c0001t0011g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.385-2277C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491699 | |||||||
chr16:84491707 | G | A | 1 | a0001c0001t0011g0349 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.385-2285C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491707 | |||||||
chr16:84491708 | T | G | 413 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(410): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.385-2286A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491708 | |||||||
chr16:84491755 | G | A | 1 | a0002c0003t0014g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.385-2333C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491755 | |||||||
chr16:84491764 | G | A | 1 | a0003c0004t0028g0424 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.385-2342C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491764 | |||||||
chr16:84491769 | C | T | 1 | a0001c0001t0160g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.385-2347G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491769 | |||||||
chr16:84491792 | G | A | 7 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-2370C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491792 | |||||||
chr16:84491793 | C | T | 1 | a0002c0016t0051g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.385-2371G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491793 | |||||||
chr16:84491813 | G | A | 2 | a0001c0001t0013g0254 a0001c0001t0013g0255 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385-2391C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491813 | |||||||
chr16:84491814 | G | C | 73 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(70): Show |
82 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.385-2392C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491814 | |||||||
chr16:84491821 | C | T | 2 | a0009c0036t0099g0017 a0009c0037t0114g0386 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.385-2399G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491821 | |||||||
chr16:84491831 | C | T | 5 | a0002c0013t0025g0018 a0002c0013t0025g0104 a0002c0013t0025g0105 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2409G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491831 | |||||||
chr16:84491836 | C | CA | 11 | a0002c0003t0006g0131 a0002c0003t0015g0132 a0003c0004t0018g0411 others(8): Show |
11 | HG01081.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.385-2415dupT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491836 | |||||||
chr16:84491836 | CA | C | 222 | a0001c0001t0001g0055 a0001c0001t0001g0083 a0001c0001t0001g0089 others(219): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.385-2415delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491836 | |||||||
chr16:84491911 | C | A | 1 | a0001c0001t0005g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.385-2489G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491911 | |||||||
chr16:84491931 | G | C | 7 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-2509C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491931 | |||||||
chr16:84491944 | T | G | 1 | a0004c0011t0096g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385-2522A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491944 | |||||||
chr16:84491982 | T | A | 1 | a0001c0001t0005g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.385-2560A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84491982 | |||||||
chr16:84492029 | T | A | 5 | a0004c0011t0092g0366 a0004c0011t0094g0370 a0004c0011t0095g0372 others(2): Show |
5 | HG02630.hp2 HG02970.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2607A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492029 | |||||||
chr16:84492068 | G | C | 59 | a0002c0003t0001g0122 a0002c0003t0001g0154 a0002c0003t0006g0131 others(56): Show |
68 | HG00423.hp2 HG00639.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.385-2646C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492068 | |||||||
chr16:84492104 | T | G | 97 | a0001c0001t0004g0305 a0001c0002t0001g0011 a0001c0002t0001g0020 others(94): Show |
98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.385-2682A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492104 | |||||||
chr16:84492127 | A | C | 1 | a0001c0001t0009g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.385-2705T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492127 | |||||||
chr16:84492156 | C | T | 3 | a0002c0019t0027g0402 a0002c0019t0027g0418 a0002c0035t0027g0433 |
3 | HG02622.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385-2734G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492156 | |||||||
chr16:84492157 | G | A | 1 | a0003c0004t0138g0342 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.385-2735C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492157 | |||||||
chr16:84492207 | A | G | 15 | a0002c0009t0020g0382 a0002c0009t0020g0383 a0002c0009t0020g0385 others(12): Show |
15 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.385-2785T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492207 | |||||||
chr16:84492285 | A | C | 225 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(222): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.385-2863T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492285 | |||||||
chr16:84492337 | C | T | 224 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.385-2915G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492337 | |||||||
chr16:84492340 | C | G | 1 | a0001c0001t0006g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.385-2918G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492340 | |||||||
chr16:84492367 | T | C | 1 | a0001c0001t0173g0420 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.385-2945A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492367 | |||||||
chr16:84492424 | G | A | 2 | a0002c0003t0010g0198 a0002c0003t0122g0199 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.385-3002C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492424 | |||||||
chr16:84492430 | T | C | 4 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-3008A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492430 | |||||||
chr16:84492492 | C | T | 1 | a0001c0001t0105g0186 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.385-3070G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492492 | |||||||
chr16:84492569 | T | TTTAATTT others(13): Show |
2 | a0001c0001t0001g0393 a0001c0001t0012g0408 |
2 | NA18940.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.384+3113_384+3114i others(22): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492569 | T | TTTTA | 15 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(12): Show |
16 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.384+3110_384+3113d others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492569 | T | TTTTATTT others(1): Show |
50 | a0001c0001t0229g0449 a0001c0005t0071g0407 a0001c0005t0129g0413 others(47): Show |
57 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.384+3106_384+3113d others(10): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492569 | T | TTTTATTT others(5): Show |
26 | a0001c0001t0100g0429 a0001c0001t0101g0187 a0001c0001t0102g0350 others(23): Show |
28 | HG01099.hp2 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.384+3102_384+3113d others(14): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492569 | T | TTTTATTT others(9): Show |
142 | a0001c0001t0001g0037 a0001c0001t0001g0083 a0001c0001t0001g0267 others(139): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.384+3098_384+3113d others(18): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492569 | T | TTTTATTT others(13): Show |
61 | a0001c0001t0001g0055 a0001c0001t0001g0089 a0001c0001t0001g0240 others(58): Show |
61 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.384+3094_384+3113d others(22): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492569 | T | TTTTATTT others(17): Show |
1 | a0001c0001t0011g0056 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.384+3090_384+3113d others(26): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492569 | |||||||
chr16:84492595 | T | TTATTTAT others(11): Show |
1 | a0001c0001t0021g0163 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.384+3087_384+3088i others(20): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492595 | |||||||
chr16:84492674 | C | T | 1 | a0002c0003t0049g0005 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.384+3009G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492674 | |||||||
chr16:84492789 | C | T | 7 | a0001c0005t0071g0407 a0001c0005t0129g0413 a0001c0005t0130g0431 others(4): Show |
7 | HG02559.hp2 HG02723.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+2894G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492789 | |||||||
chr16:84492794 | C | A | 1 | a0004c0011t0092g0366 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.384+2889G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492794 | |||||||
chr16:84492811 | A | C | 1 | a0001c0001t0197g0259 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.384+2872T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492811 | |||||||
chr16:84492829 | A | G | 443 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(440): Show |
462 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(459): Show |
intron_variant | MODIFIER | c.384+2854T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492829 | |||||||
chr16:84492852 | C | G | 224 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(221): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.384+2831G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492852 | |||||||
chr16:84492864 | C | G | 288 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(285): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.384+2819G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492864 | |||||||
chr16:84492900 | C | T | 1 | a0001c0001t0203g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.384+2783G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84492900 | |||||||
chr16:84493025 | C | G | 2 | a0001c0006t0043g0215 a0001c0006t0043g0331 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.384+2658G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493025 | |||||||
chr16:84493118 | T | C | 1 | a0015c0038t0052g0343 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.384+2565A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493118 | |||||||
chr16:84493157 | T | C | 3 | a0001c0005t0071g0407 a0001c0005t0129g0413 a0001c0005t0130g0431 |
3 | HG03225.hp1 NA18522.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.384+2526A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493157 | |||||||
chr16:84493277 | T | C | 1 | a0004c0011t0095g0372 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.384+2406A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493277 | |||||||
chr16:84493316 | T | C | 2 | a0014c0025t0224g0447 a0015c0038t0052g0343 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.384+2367A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493316 | |||||||
chr16:84493327 | A | G | 293 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(290): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.384+2356T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493327 | |||||||
chr16:84493359 | C | T | 281 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(278): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.384+2324G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493359 | |||||||
chr16:84493395 | T | C | 443 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(440): Show |
462 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(459): Show |
intron_variant | MODIFIER | c.384+2288A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493395 | |||||||
chr16:84493408 | G | C | 97 | a0001c0001t0001g0099 a0001c0001t0004g0305 a0001c0001t0045g0015 others(94): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.384+2275C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493408 | |||||||
chr16:84493415 | C | T | 101 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(98): Show |
112 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.384+2268G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493415 | |||||||
chr16:84493433 | C | A | 2 | a0001c0002t0056g0319 a0001c0002t0056g0320 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.384+2250G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493433 | |||||||
chr16:84493973 | A | G | 1 | a0001c0002t0214g0290 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.384+1710T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84493973 | |||||||
chr16:84494025 | G | T | 1 | a0004c0020t0121g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384+1658C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494025 | |||||||
chr16:84494195 | A | G | 3 | a0001c0002t0002g0027 a0001c0002t0004g0026 a0001c0002t0004g0106 |
3 | NA18971.hp2 NA18975.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.384+1488T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494195 | |||||||
chr16:84494205 | C | A | 275 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(272): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.384+1478G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494205 | |||||||
chr16:84494253 | G | C | 5 | a0004c0011t0092g0366 a0004c0011t0094g0370 a0004c0011t0095g0372 others(2): Show |
5 | HG02630.hp2 HG02970.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+1430C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494253 | |||||||
chr16:84494280 | T | C | 1 | a0001c0001t0160g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.384+1403A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494280 | |||||||
chr16:84494303 | A | G | 110 | a0001c0001t0001g0364 a0001c0001t0001g0393 a0001c0001t0004g0305 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.384+1380T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494303 | |||||||
chr16:84494513 | C | T | 2 | a0002c0003t0047g0376 a0002c0003t0047g0377 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.384+1170G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494513 | |||||||
chr16:84494629 | T | C | 68 | a0001c0001t0006g0241 a0001c0001t0013g0389 a0001c0001t0186g0164 others(65): Show |
77 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.384+1054A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494629 | |||||||
chr16:84494687 | C | T | 60 | a0001c0001t0229g0449 a0001c0006t0043g0215 a0001c0006t0043g0331 others(57): Show |
68 | HG00423.hp2 HG00673.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.384+996G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494687 | |||||||
chr16:84494711 | G | C | 422 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(419): Show |
441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.384+972C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494711 | |||||||
chr16:84494839 | G | C | 2 | a0001c0002t0063g0287 a0001c0002t0063g0288 |
2 | NA18948.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.384+844C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84494839 | |||||||
chr16:84495011 | A | G | 1 | a0021c0031t0219g0112 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.384+672T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495011 | |||||||
chr16:84495055 | G | A | 1 | a0001c0001t0036g0116 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.384+628C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495055 | |||||||
chr16:84495097 | C | T | 61 | a0001c0001t0203g0220 a0001c0001t0229g0449 a0001c0006t0043g0215 others(58): Show |
69 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.384+586G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495097 | |||||||
chr16:84495114 | C | G | 1 | a0001c0006t0113g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.384+569G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495114 | |||||||
chr16:84495225 | C | T | 2 | a0002c0016t0051g0216 a0002c0016t0051g0217 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.384+458G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495225 | |||||||
chr16:84495261 | T | G | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.384+422A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495261 | |||||||
chr16:84495326 | T | A | 1 | a0001c0001t0147g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.384+357A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495326 | |||||||
chr16:84495352 | C | A | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.384+331G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495352 | |||||||
chr16:84495355 | G | A | 1 | a0001c0001t0005g0380 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.384+328C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495355 | |||||||
chr16:84495442 | C | T | 3 | a0001c0005t0140g0432 a0001c0005t0141g0348 a0021c0031t0219g0112 |
3 | HG02559.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.384+241G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495442 | |||||||
chr16:84495443 | C | T | 1 | a0018c0029t0205g0405 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.384+240G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495443 | |||||||
chr16:84495462 | G | C | 441 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(438): Show |
460 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(457): Show |
intron_variant | MODIFIER | c.384+221C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495462 | |||||||
chr16:84495670 | G | A | 11 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(8): Show |
11 | HG01069.hp1 HG01361.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.384+13C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | 84495670 | |||||||
chr16:84495965 | G | C | 1 | a0002c0003t0029g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.154-52C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84495965 | |||||||
chr16:84495980 | T | C | 1 | a0001c0001t0154g0068 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.154-67A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84495980 | |||||||
chr16:84495988 | G | C | 2 | a0002c0003t0136g0347 a0002c0003t0139g0115 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-75C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84495988 | |||||||
chr16:84496108 | G | A | 1 | a0001c0001t0209g0381 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.154-195C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496108 | |||||||
chr16:84496190 | C | T | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-277G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496190 | |||||||
chr16:84496191 | G | A | 8 | a0001c0005t0071g0407 a0001c0005t0129g0413 a0001c0005t0130g0431 others(5): Show |
8 | HG02258.hp1 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-278C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496191 | |||||||
chr16:84496208 | C | G | 5 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-295G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496208 | |||||||
chr16:84496208 | C | T | 5 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0002c0019t0027g0402 others(2): Show |
5 | HG02622.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-295G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496208 | |||||||
chr16:84496437 | C | A | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-524G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496437 | |||||||
chr16:84496457 | G | A | 10 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(7): Show |
10 | HG02572.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-544C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496457 | |||||||
chr16:84496490 | C | T | 1 | a0002c0003t0212g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.154-577G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496490 | |||||||
chr16:84496536 | C | T | 1 | a0001c0005t0003g0040 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.154-623G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496536 | |||||||
chr16:84496549 | C | G | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.154-636G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496549 | |||||||
chr16:84496583 | C | T | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-670G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496583 | |||||||
chr16:84496626 | A | T | 10 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(7): Show |
10 | HG02572.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-713T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496626 | |||||||
chr16:84496703 | G | A | 2 | a0002c0003t0093g0437 a0002c0003t0115g0438 |
2 | HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.154-790C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496703 | |||||||
chr16:84496775 | C | T | 22 | a0002c0003t0093g0437 a0002c0003t0115g0438 a0003c0004t0018g0033 others(19): Show |
22 | HG00735.hp1 HG01169.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.154-862G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496775 | |||||||
chr16:84496776 | C | T | 2 | a0002c0003t0093g0437 a0002c0003t0115g0438 |
2 | HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.154-863G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496776 | |||||||
chr16:84496841 | A | G | 2 | a0002c0003t0136g0347 a0002c0003t0139g0115 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-928T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496841 | |||||||
chr16:84496891 | C | T | 2 | a0009c0036t0099g0017 a0009c0037t0114g0386 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.154-978G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496891 | |||||||
chr16:84496893 | G | C | 2 | a0009c0036t0099g0017 a0009c0037t0114g0386 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.154-980C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496893 | |||||||
chr16:84496907 | A | G | 5 | a0004c0011t0092g0366 a0004c0011t0094g0370 a0004c0011t0095g0372 others(2): Show |
5 | HG02630.hp2 HG02970.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-994T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84496907 | |||||||
chr16:84497008 | A | G | 3 | a0001c0005t0003g0040 a0001c0005t0003g0041 a0001c0005t0064g0039 |
3 | HG00323.hp2 HG02015.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.153+926T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497008 | |||||||
chr16:84497138 | C | T | 443 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(440): Show |
462 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(459): Show |
intron_variant | MODIFIER | c.153+796G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497138 | |||||||
chr16:84497148 | G | C | 1 | a0001c0005t0141g0348 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.153+786C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497148 | |||||||
chr16:84497185 | A | G | 1 | a0001c0001t0006g0392 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.153+749T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497185 | |||||||
chr16:84497187 | G | A | 5 | a0002c0013t0025g0018 a0002c0013t0025g0104 a0002c0013t0025g0105 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+747C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497187 | |||||||
chr16:84497277 | A | C | 47 | a0001c0001t0001g0055 a0001c0001t0001g0089 a0001c0001t0001g0099 others(44): Show |
49 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.153+657T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497277 | |||||||
chr16:84497367 | T | G | 5 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+567A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497367 | |||||||
chr16:84497409 | A | C | 2 | a0008c0014t0010g0014 a0008c0014t0046g0369 |
3 | HG01070.hp1 HG01071.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.153+525T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497409 | |||||||
chr16:84497433 | A | C | 1 | a0001c0006t0069g0446 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.153+501T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497433 | |||||||
chr16:84497465 | C | T | 91 | a0001c0001t0004g0305 a0001c0001t0178g0286 a0001c0002t0001g0011 others(88): Show |
92 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.153+469G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497465 | |||||||
chr16:84497476 | G | A | 1 | a0001c0001t0075g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.153+458C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497476 | |||||||
chr16:84497476 | G | C | 5 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+458C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497476 | |||||||
chr16:84497600 | G | A | 16 | a0002c0003t0139g0115 a0002c0009t0020g0382 a0002c0009t0020g0383 others(13): Show |
16 | HG01175.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.153+334C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497600 | |||||||
chr16:84497670 | T | C | 1 | a0001c0001t0013g0389 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153+264A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497670 | |||||||
chr16:84497701 | G | C | 236 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(233): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.153+233C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497701 | |||||||
chr16:84497840 | A | G | 7 | a0002c0003t0135g0114 a0005c0008t0090g0204 a0005c0008t0098g0338 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+94T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497840 | |||||||
chr16:84497891 | C | G | 7 | a0002c0003t0139g0115 a0002c0009t0020g0382 a0002c0009t0020g0383 others(4): Show |
7 | HG01175.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+43G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 2/7 | chr16 | 84497891 | |||||||
chr16:84498134 | A | T | 1 | a0001c0001t0170g0327 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-25-23T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498134 | |||||||
chr16:84498140 | A | T | 26 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(23): Show |
26 | HG01175.hp2 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-25-29T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498140 | |||||||
chr16:84498161 | C | A | 86 | a0001c0001t0004g0305 a0001c0001t0178g0286 a0001c0002t0001g0011 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-25-50G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498161 | |||||||
chr16:84498174 | T | C | 268 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(265): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.-25-63A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498174 | |||||||
chr16:84498210 | T | C | 1 | a0015c0038t0052g0343 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-25-99A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498210 | |||||||
chr16:84498216 | C | A | 1 | a0001c0002t0153g0321 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-25-105G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498216 | |||||||
chr16:84498218 | A | C | 1 | a0002c0003t0207g0119 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-25-107T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498218 | |||||||
chr16:84498268 | G | C | 7 | a0004c0011t0092g0366 a0004c0011t0094g0370 a0004c0011t0095g0372 others(4): Show |
7 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25-157C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498268 | |||||||
chr16:84498315 | C | A | 1 | a0001c0001t0228g0443 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-25-204G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498315 | |||||||
chr16:84498394 | G | C | 24 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(21): Show |
24 | HG01175.hp2 HG02109.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.-25-283C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498394 | |||||||
chr16:84498435 | A | ATT | 16 | a0002c0003t0139g0115 a0002c0009t0020g0382 a0002c0009t0020g0383 others(13): Show |
16 | HG01175.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25-326_-25-325dup others(2): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498435 | |||||||
chr16:84498435 | A | ATTT | 10 | a0001c0006t0043g0215 a0001c0006t0043g0331 a0001c0006t0044g0181 others(7): Show |
10 | HG02572.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-327_-25-325dup others(3): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498435 | |||||||
chr16:84498506 | C | G | 2 | a0009c0036t0099g0017 a0009c0037t0114g0386 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25-395G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498506 | |||||||
chr16:84498509 | A | C | 11 | a0002c0003t0135g0114 a0002c0010t0040g0010 a0002c0010t0044g0346 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-398T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498509 | |||||||
chr16:84498514 | A | G | 91 | a0001c0001t0004g0305 a0001c0001t0178g0286 a0001c0002t0001g0011 others(88): Show |
92 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-25-403T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498514 | |||||||
chr16:84498552 | G | C | 1 | a0003c0004t0018g0337 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-25-441C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498552 | |||||||
chr16:84498674 | C | CTCAA | 2 | a0001c0001t0008g0013 a0001c0001t0008g0360 |
3 | NA18988.hp1 NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-25-564_-25-563ins others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498674 | |||||||
chr16:84498696 | A | T | 234 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(231): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.-25-585T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498696 | |||||||
chr16:84498717 | T | C | 421 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(418): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.-25-606A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498717 | |||||||
chr16:84498929 | A | C | 3 | a0002c0019t0027g0402 a0002c0019t0027g0418 a0002c0035t0027g0433 |
3 | HG02622.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-818T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498929 | |||||||
chr16:84498994 | G | A | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-25-883C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498994 | |||||||
chr16:84498995 | C | G | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-25-884G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84498995 | |||||||
chr16:84499040 | C | A | 1 | a0001c0002t0001g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-25-929G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499040 | |||||||
chr16:84499052 | C | T | 3 | a0001c0005t0071g0407 a0001c0005t0129g0413 a0001c0005t0130g0431 |
3 | HG03225.hp1 NA18522.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-25-941G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499052 | |||||||
chr16:84499074 | G | A | 1 | a0003c0004t0107g0436 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-25-963C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499074 | |||||||
chr16:84499078 | G | A | 1 | a0001c0001t0011g0349 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-25-967C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499078 | |||||||
chr16:84499100 | G | A | 1 | a0004c0020t0121g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-989C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499100 | |||||||
chr16:84499142 | G | T | 53 | a0001c0001t0229g0449 a0001c0002t0006g0143 a0001c0005t0129g0413 others(50): Show |
61 | HG00423.hp2 HG00639.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-25-1031C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499142 | |||||||
chr16:84499143 | G | C | 1 | a0001c0001t0060g0270 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-25-1032C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499143 | |||||||
chr16:84499185 | G | T | 3 | a0002c0019t0027g0402 a0002c0019t0027g0418 a0002c0035t0027g0433 |
3 | HG02622.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-1074C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499185 | |||||||
chr16:84499267 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-25-1156A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499267 | |||||||
chr16:84499495 | A | G | 203 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(200): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-25-1384T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499495 | |||||||
chr16:84499500 | A | C | 2 | a0002c0003t0093g0437 a0002c0003t0115g0438 |
2 | HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-25-1389T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499500 | |||||||
chr16:84499507 | A | G | 202 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(199): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-25-1396T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499507 | |||||||
chr16:84499508 | T | A | 202 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(199): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-25-1397A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499508 | |||||||
chr16:84499539 | A | C | 197 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(194): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.-25-1428T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499539 | |||||||
chr16:84499539 | A | G | 3 | a0001c0001t0021g0163 a0001c0001t0223g0441 a0001c0017t0175g0183 |
3 | HG00438.hp2 HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-25-1428T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499539 | |||||||
chr16:84499637 | C | G | 4 | a0002c0019t0027g0402 a0002c0019t0027g0418 a0002c0035t0027g0433 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-1526G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499637 | |||||||
chr16:84499774 | C | T | 1 | a0001c0002t0006g0289 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-25-1663G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499774 | |||||||
chr16:84499837 | G | C | 1 | a0007c0012t0037g0332 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-25-1726C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499837 | |||||||
chr16:84499890 | C | A | 2 | a0001c0002t0006g0143 a0002c0003t0007g0138 |
2 | HG00673.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.-25-1779G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499890 | |||||||
chr16:84499910 | G | T | 5 | a0001c0001t0102g0350 a0002c0013t0025g0104 a0002c0013t0025g0105 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-1799C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499910 | |||||||
chr16:84499947 | G | C | 341 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(338): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.-25-1836C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499947 | |||||||
chr16:84499947 | G | T | 1 | a0002c0003t0136g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-25-1836C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499947 | |||||||
chr16:84499954 | G | C | 102 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(99): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-25-1843C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499954 | |||||||
chr16:84499979 | G | T | 11 | a0001c0001t0001g0240 a0001c0001t0004g0236 a0001c0001t0006g0241 others(8): Show |
11 | HG00323.hp2 HG00558.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-1868C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499979 | |||||||
chr16:84499998 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-25-1887G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84499998 | |||||||
chr16:84500013 | G | C | 92 | a0001c0001t0003g0080 a0001c0001t0004g0305 a0001c0001t0045g0015 others(89): Show |
94 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-25-1902C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500013 | |||||||
chr16:84500023 | CA | C | 7 | a0001c0001t0005g0375 a0001c0001t0005g0380 a0002c0003t0047g0376 others(4): Show |
7 | HG00099.hp1 HG01255.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-1913delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500023 | |||||||
chr16:84500054 | G | C | 1 | a0001c0001t0004g0081 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-25-1943C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500054 | |||||||
chr16:84500066 | G | A | 69 | a0001c0001t0004g0305 a0001c0001t0045g0015 a0001c0002t0001g0011 others(66): Show |
71 | HG00140.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-25-1955C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500066 | |||||||
chr16:84500091 | T | C | 235 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(232): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-25-1980A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500091 | |||||||
chr16:84500099 | G | C | 1 | a0002c0003t0136g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-25-1988C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500099 | |||||||
chr16:84500129 | T | C | 1 | a0001c0001t0003g0024 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-25-2018A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500129 | |||||||
chr16:84500133 | G | A | 2 | a0001c0001t0001g0364 a0001c0001t0002g0365 |
2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-25-2022C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500133 | |||||||
chr16:84500169 | G | A | 68 | a0001c0001t0001g0037 a0001c0001t0001g0083 a0001c0001t0001g0267 others(65): Show |
71 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-25-2058C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500169 | |||||||
chr16:84500246 | G | A | 1 | a0001c0001t0184g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-25-2135C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500246 | |||||||
chr16:84500374 | G | A | 1 | a0002c0009t0227g0444 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-25-2263C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500374 | |||||||
chr16:84500399 | C | G | 2 | a0002c0003t0093g0437 a0002c0003t0115g0438 |
2 | HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-25-2288G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500399 | |||||||
chr16:84500444 | G | T | 2 | a0003c0004t0226g0442 a0007c0012t0037g0332 |
2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-25-2333C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500444 | |||||||
chr16:84500445 | C | T | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-25-2334G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500445 | |||||||
chr16:84500469 | T | C | 252 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(249): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-25-2358A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500469 | |||||||
chr16:84500474 | C | G | 253 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(250): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-25-2363G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500474 | |||||||
chr16:84500480 | T | C | 253 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(250): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-25-2369A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500480 | |||||||
chr16:84500532 | C | G | 1 | a0003c0004t0226g0442 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-25-2421G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500532 | |||||||
chr16:84500554 | T | C | 1 | a0001c0001t0104g0344 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-25-2443A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500554 | |||||||
chr16:84500591 | G | A | 71 | a0001c0001t0004g0305 a0001c0001t0045g0015 a0001c0001t0075g0184 others(68): Show |
73 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-25-2480C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500591 | |||||||
chr16:84500646 | G | C | 175 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0004g0305 others(172): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-25-2535C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500646 | |||||||
chr16:84500675 | G | A | 1 | a0002c0003t0007g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-25-2564C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500675 | |||||||
chr16:84500760 | G | A | 119 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(116): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-25-2649C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500760 | |||||||
chr16:84500760 | G | C | 1 | a0001c0001t0172g0038 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-25-2649C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500760 | |||||||
chr16:84500775 | G | A | 11 | a0001c0006t0044g0181 a0001c0006t0069g0445 a0001c0006t0069g0446 others(8): Show |
11 | HG02109.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25-2664C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500775 | |||||||
chr16:84500827 | A | C | 2 | a0001c0001t0053g0434 a0001c0001t0053g0435 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-25-2716T>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500827 | |||||||
chr16:84500853 | G | C | 74 | a0001c0001t0004g0305 a0001c0001t0045g0015 a0001c0001t0178g0286 others(71): Show |
76 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-25-2742C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500853 | |||||||
chr16:84500983 | T | G | 127 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(124): Show |
139 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-25-2872A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84500983 | |||||||
chr16:84501039 | G | A | 1 | a0009c0036t0099g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-25-2928C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501039 | |||||||
chr16:84501058 | A | G | 445 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(442): Show |
464 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(461): Show |
intron_variant | MODIFIER | c.-25-2947T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501058 | |||||||
chr16:84501088 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-25-2977G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501088 | |||||||
chr16:84501105 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-25-2994C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501105 | |||||||
chr16:84501105 | G | GA | 94 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(91): Show |
102 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-25-2995dupT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501105 | |||||||
chr16:84501105 | GAA | G | 7 | a0001c0001t0004g0236 a0001c0001t0011g0049 a0001c0001t0054g0416 others(4): Show |
7 | HG01169.hp2 HG02027.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-2996_-25-2995d others(4): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501105 | |||||||
chr16:84501105 | GAAA | G | 213 | a0001c0001t0001g0055 a0001c0001t0001g0083 a0001c0001t0001g0089 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-25-2997_-25-2995d others(5): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501105 | |||||||
chr16:84501105 | GAAAA | G | 77 | a0001c0001t0003g0024 a0001c0001t0004g0305 a0001c0001t0009g0158 others(74): Show |
79 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-25-2998_-25-2995d others(6): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501105 | |||||||
chr16:84501108 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0172g0038 |
2 | NA18955.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-25-2997T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501108 | |||||||
chr16:84501155 | T | C | 414 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(411): Show |
432 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(429): Show |
intron_variant | MODIFIER | c.-25-3044A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501155 | |||||||
chr16:84501169 | G | C | 10 | a0001c0005t0129g0413 a0001c0005t0130g0431 a0001c0005t0140g0432 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25-3058C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501169 | |||||||
chr16:84501171 | G | A | 1 | a0001c0005t0140g0432 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-25-3060C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501171 | |||||||
chr16:84501190 | G | T | 220 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(217): Show |
227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-25-3079C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501190 | |||||||
chr16:84501260 | T | C | 5 | a0003c0004t0052g0340 a0003c0004t0108g0341 a0003c0004t0138g0342 others(2): Show |
5 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-3149A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501260 | |||||||
chr16:84501263 | G | C | 182 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0004g0305 others(179): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-25-3152C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501263 | |||||||
chr16:84501293 | G | A | 1 | a0001c0001t0104g0344 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-25-3182C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501293 | |||||||
chr16:84501295 | T | C | 419 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(416): Show |
437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
intron_variant | MODIFIER | c.-25-3184A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501295 | |||||||
chr16:84501424 | G | C | 219 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(216): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-26+3177C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501424 | |||||||
chr16:84501504 | C | T | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-26+3097G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501504 | |||||||
chr16:84501514 | G | A | 1 | a0001c0001t0011g0349 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-26+3087C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501514 | |||||||
chr16:84501556 | G | C | 94 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(91): Show |
104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-26+3045C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501556 | |||||||
chr16:84501574 | G | A | 16 | a0001c0001t0104g0344 a0001c0002t0143g0326 a0002c0009t0227g0444 others(13): Show |
17 | HG00735.hp1 HG01358.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-26+3027C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501574 | |||||||
chr16:84501703 | C | G | 1 | a0008c0014t0046g0369 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-26+2898G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501703 | |||||||
chr16:84501727 | C | T | 1 | a0001c0002t0006g0277 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-26+2874G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501727 | |||||||
chr16:84501742 | G | A | 1 | a0002c0009t0227g0444 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-26+2859C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501742 | |||||||
chr16:84501748 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-26+2853G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501748 | |||||||
chr16:84501749 | A | G | 276 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(273): Show |
284 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-26+2852T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501749 | |||||||
chr16:84501760 | A | G | 34 | a0001c0001t0030g0335 a0001c0001t0030g0336 a0001c0001t0104g0344 others(31): Show |
35 | HG00735.hp1 HG01358.hp2 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.-26+2841T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501760 | |||||||
chr16:84501808 | C | G | 71 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(68): Show |
75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-26+2793G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501808 | |||||||
chr16:84501913 | G | C | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-26+2688C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501913 | |||||||
chr16:84501966 | G | A | 4 | a0001c0005t0129g0413 a0001c0005t0130g0431 a0001c0005t0140g0432 others(1): Show |
4 | HG03225.hp1 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+2635C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84501966 | |||||||
chr16:84502004 | T | C | 415 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(412): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.-26+2597A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502004 | |||||||
chr16:84502018 | C | T | 7 | a0002c0003t0135g0114 a0002c0019t0027g0418 a0002c0035t0027g0433 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26+2583G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502018 | |||||||
chr16:84502054 | G | A | 1 | a0001c0002t0012g0225 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-26+2547C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502054 | |||||||
chr16:84502144 | C | CA | 95 | a0001c0001t0004g0305 a0001c0001t0030g0335 a0001c0001t0030g0336 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-26+2456dupT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502144 | |||||||
chr16:84502184 | C | G | 208 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0004g0305 others(205): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-26+2417G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502184 | |||||||
chr16:84502227 | G | A | 8 | a0001c0001t0100g0429 a0002c0003t0067g0426 a0002c0013t0025g0018 others(5): Show |
8 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26+2374C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502227 | |||||||
chr16:84502244 | G | A | 1 | a0007c0012t0037g0332 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-26+2357C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502244 | |||||||
chr16:84502268 | G | C | 1 | a0001c0005t0179g0403 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-26+2333C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502268 | |||||||
chr16:84502338 | T | TA | 221 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(218): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-26+2262dupT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502338 | |||||||
chr16:84502373 | G | A | 29 | a0001c0001t0030g0335 a0001c0001t0030g0336 a0001c0001t0104g0344 others(26): Show |
30 | HG00735.hp1 HG01358.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.-26+2228C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502373 | |||||||
chr16:84502422 | G | C | 98 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(95): Show |
108 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.-26+2179C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502422 | |||||||
chr16:84502445 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-26+2156C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502445 | |||||||
chr16:84502447 | A | G | 1 | a0003c0004t0226g0442 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-26+2154T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502447 | |||||||
chr16:84502460 | C | T | 225 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(222): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-26+2141G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502460 | |||||||
chr16:84502688 | T | C | 1 | a0001c0001t0012g0408 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-26+1913A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502688 | |||||||
chr16:84502728 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-26+1873C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502728 | |||||||
chr16:84502775 | G | T | 2 | a0001c0001t0017g0149 a0001c0001t0017g0150 |
2 | NA18963.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-26+1826C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502775 | |||||||
chr16:84502778 | G | T | 3 | a0007c0012t0037g0367 a0007c0012t0084g0113 a0021c0031t0219g0112 |
3 | HG01884.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-26+1823C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502778 | |||||||
chr16:84502805 | G | T | 40 | a0001c0001t0024g0135 a0001c0001t0036g0136 a0001c0002t0001g0137 others(37): Show |
47 | HG00423.hp2 HG00673.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-26+1796C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502805 | |||||||
chr16:84502853 | G | C | 1 | a0004c0020t0142g0409 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-26+1748C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502853 | |||||||
chr16:84502916 | G | C | 1 | a0001c0005t0129g0413 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-26+1685C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502916 | |||||||
chr16:84502919 | G | T | 11 | a0001c0001t0101g0187 a0001c0001t0103g0412 a0001c0005t0129g0413 others(8): Show |
11 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26+1682C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502919 | |||||||
chr16:84502968 | T | A | 1 | a0001c0001t0170g0327 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-26+1633A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502968 | |||||||
chr16:84502981 | T | C | 1 | a0011c0024t0004g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-26+1620A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84502981 | |||||||
chr16:84503003 | A | G | 1 | a0001c0001t0017g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-26+1598T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503003 | |||||||
chr16:84503013 | A | G | 97 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(94): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-26+1588T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503013 | |||||||
chr16:84503078 | C | G | 103 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(100): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-26+1523G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503078 | |||||||
chr16:84503087 | T | G | 52 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(49): Show |
55 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-26+1514A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503087 | |||||||
chr16:84503100 | G | C | 1 | a0001c0001t0003g0100 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-26+1501C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503100 | |||||||
chr16:84503104 | T | C | 52 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(49): Show |
55 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-26+1497A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503104 | |||||||
chr16:84503205 | G | A | 2 | a0003c0004t0018g0410 a0003c0004t0018g0411 |
2 | HG01433.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-26+1396C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503205 | |||||||
chr16:84503206 | TA | T | 438 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(435): Show |
457 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(454): Show |
intron_variant | MODIFIER | c.-26+1394delT | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503206 | |||||||
chr16:84503208 | A | T | 3 | a0001c0002t0001g0224 a0001c0002t0002g0223 a0001c0002t0012g0225 |
3 | HG01261.hp1 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-26+1393T>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503208 | |||||||
chr16:84503234 | G | C | 1 | a0001c0002t0001g0103 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-26+1367C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503234 | |||||||
chr16:84503240 | G | C | 2 | a0002c0013t0025g0018 a0009c0036t0099g0017 |
2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-26+1361C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503240 | |||||||
chr16:84503281 | T | C | 328 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(325): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-26+1320A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503281 | |||||||
chr16:84503291 | G | A | 14 | a0001c0001t0054g0415 a0001c0001t0054g0416 a0001c0001t0101g0187 others(11): Show |
14 | HG02027.hp2 HG02083.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26+1310C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503291 | |||||||
chr16:84503299 | C | T | 54 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0006g0213 others(51): Show |
57 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-26+1302G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503299 | |||||||
chr16:84503384 | C | T | 40 | a0001c0001t0006g0213 a0001c0001t0024g0211 a0001c0001t0035g0206 others(37): Show |
41 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-26+1217G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503384 | |||||||
chr16:84503407 | C | T | 435 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(432): Show |
454 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(451): Show |
intron_variant | MODIFIER | c.-26+1194G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503407 | |||||||
chr16:84503447 | C | T | 1 | a0001c0001t0203g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-26+1154G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503447 | |||||||
chr16:84503473 | G | C | 9 | a0001c0001t0006g0213 a0001c0001t0024g0211 a0001c0001t0035g0206 others(6): Show |
9 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+1128C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503473 | |||||||
chr16:84503580 | C | A | 99 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(96): Show |
105 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-26+1021G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503580 | |||||||
chr16:84503617 | C | T | 5 | a0001c0001t0011g0349 a0001c0001t0102g0350 a0001c0005t0141g0348 others(2): Show |
5 | HG00741.hp2 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+984G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503617 | |||||||
chr16:84503627 | G | C | 3 | a0001c0001t0053g0434 a0001c0001t0053g0435 a0001c0002t0006g0417 |
3 | HG00140.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-26+974C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503627 | |||||||
chr16:84503660 | G | A | 1 | a0010c0022t0057g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-26+941C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503660 | |||||||
chr16:84503758 | T | C | 2 | a0002c0003t0093g0437 a0002c0003t0115g0438 |
2 | HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-26+843A>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503758 | |||||||
chr16:84503817 | C | A | 1 | a0001c0017t0175g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-26+784G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503817 | |||||||
chr16:84503849 | G | T | 2 | a0002c0003t0136g0347 a0002c0010t0044g0346 |
2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-26+752C>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503849 | |||||||
chr16:84503850 | C | T | 1 | a0002c0019t0027g0418 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-26+751G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503850 | |||||||
chr16:84503921 | C | A | 109 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(106): Show |
115 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-26+680G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84503921 | |||||||
chr16:84504010 | C | T | 85 | a0001c0001t0001g0364 a0001c0001t0001g0393 a0001c0001t0002g0365 others(82): Show |
89 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-26+591G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504010 | |||||||
chr16:84504022 | C | G | 7 | a0001c0001t0228g0443 a0001c0006t0069g0445 a0001c0006t0069g0446 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+579G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504022 | |||||||
chr16:84504024 | G | C | 1 | a0007c0012t0076g0345 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26+577C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504024 | |||||||
chr16:84504037 | C | T | 7 | a0001c0001t0104g0344 a0003c0004t0052g0340 a0003c0004t0108g0341 others(4): Show |
7 | HG02145.hp1 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26+564G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504037 | |||||||
chr16:84504038 | T | A | 270 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(267): Show |
279 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-26+563A>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504038 | |||||||
chr16:84504042 | G | A | 3 | a0002c0013t0025g0104 a0002c0013t0025g0105 a0003c0004t0107g0436 |
3 | HG02965.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-26+559C>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504042 | |||||||
chr16:84504073 | T | G | 3 | a0002c0013t0025g0104 a0002c0013t0025g0105 a0003c0004t0107g0436 |
3 | HG02965.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-26+528A>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504073 | |||||||
chr16:84504105 | C | T | 4 | a0001c0001t0030g0335 a0001c0001t0030g0336 a0003c0004t0018g0337 others(1): Show |
4 | HG02647.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+496G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504105 | |||||||
chr16:84504192 | C | A | 426 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(423): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.-26+409G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504192 | |||||||
chr16:84504193 | C | A | 1 | a0001c0002t0004g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-26+408G>T | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504193 | |||||||
chr16:84504248 | C | G | 2 | a0002c0013t0025g0018 a0009c0036t0099g0017 |
2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-26+353G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504248 | |||||||
chr16:84504311 | G | C | 2 | a0002c0003t0093g0437 a0002c0003t0115g0438 |
2 | HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-26+290C>G | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504311 | |||||||
chr16:84504316 | A | G | 5 | a0001c0001t0161g0110 a0001c0001t0166g0111 a0002c0003t0135g0114 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+285T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504316 | |||||||
chr16:84504351 | C | T | 331 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.-26+250G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504351 | |||||||
chr16:84504381 | C | G | 5 | a0001c0001t0161g0110 a0001c0001t0166g0111 a0002c0003t0135g0114 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+220G>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504381 | |||||||
chr16:84504418 | CCACCCCT others(17): Show |
C | 3 | a0001c0001t0223g0441 a0001c0002t0001g0440 a0001c0002t0002g0439 |
3 | HG00609.hp2 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-26+159_-26+182del others(24): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504418 | |||||||
chr16:84504473 | A | G | 124 | a0001c0001t0006g0213 a0001c0001t0009g0158 a0001c0001t0009g0159 others(121): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-26+128T>C | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504473 | |||||||
chr16:84504545 | C | T | 1 | a0001c0001t0009g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-26+56G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504545 | |||||||
chr16:84504582 | C | T | 95 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0083 others(92): Show |
100 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.-26+19G>A | MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 1/7 | chr16 | 84504582 |