Item | Value |
---|---|
geneid | 55556 |
ensemblid | ENSG00000132199.20 |
hgncid | 30365 |
symbol | ENOSF1 |
name | enolase superfamily member 1 |
refseq_nuc | NM_017512.7 |
refseq_prot | NP_059982.2 |
ensembl_nuc | ENST00000647584.2 |
ensembl_prot | ENSP00000497230.2 |
mane_status | MANE Select |
chr | chr18 |
start | 670318 |
end | 712630 |
strand | - |
ver | v1.2 |
region | chr18:670318-712630 |
region5000 | chr18:665318-717630 |
regionname0 | ENOSF1_chr18_670318_712630 |
regionname5000 | ENOSF1_chr18_665318_717630 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 443 | 267 | 60 | 43 | 119 | 10 | 34 | 96 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0002 | 0/1 | 443 | 82 | 24 | 26 | 17 | 3 | 11 | 10 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0003 | 0/0 | 443 | 55 | 1 | 3 | 47 | 1 | 3 | 33 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0004 | 0/0 | 443 | 7 | 0 | 4 | 0 | 3 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0005 | 0/0 | 443 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0006 | 0/0 | 195 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(190): Show |
chr18 | 665318 | 717630 |
a0007 | 0/0 | 443 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0008 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
a0009 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | MVRGR others(438): Show |
chr18 | 665318 | 717630 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1329 | 212 | 45 | 41 | 83 | 10 | 32 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0001c0003 | 0/0 | 1329 | 41 | 3 | 2 | 34 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0001c0006 | 0/0 | 1329 | 12 | 12 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0001c0013 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0001c0017 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0002c0002 | 0/1 | 1329 | 64 | 23 | 12 | 16 | 2 | 10 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0002c0005 | 0/0 | 1329 | 17 | 0 | 14 | 1 | 1 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0002c0015 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0003c0004 | 0/0 | 1329 | 40 | 0 | 3 | 36 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0003c0007 | 0/0 | 1329 | 12 | 1 | 0 | 10 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0003c0011 | 0/0 | 1329 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0003c0018 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0004c0008 | 0/0 | 1329 | 7 | 0 | 4 | 0 | 3 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0005c0010 | 0/0 | 1329 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0006c0009 | 0/0 | 988 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(983): Show |
chr18 | 665318 | 717630 | ||
a0007c0012 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0008c0014 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 | ||
a0009c0016 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | ATGGT others(1324): Show |
chr18 | 665318 | 717630 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5362 | 63 | 9 | 22 | 10 | 8 | 13 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0001t0002 | 0/0 | 5353 | 103 | 17 | 10 | 58 | 1 | 17 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0005 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5358): Show |
chr18 | 665318 | 717630 |
a0001c0001t0006 | 0/0 | 5353 | 9 | 9 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0007 | 0/0 | 5362 | 8 | 0 | 0 | 8 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0001t0010 | 0/0 | 5362 | 5 | 0 | 5 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0001t0011 | 0/0 | 5353 | 6 | 5 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0013 | 0/0 | 5353 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0014 | 0/0 | 5353 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0015 | 0/0 | 5353 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0016 | 0/0 | 5353 | 2 | 0 | 1 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0017 | 0/0 | 5353 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0019 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0001t0024 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0001t0028 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0030 | 0/0 | 5354 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5349): Show |
chr18 | 665318 | 717630 |
a0001c0001t0031 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0032 | 0/0 | 5353 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0001t0033 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5354): Show |
chr18 | 665318 | 717630 |
a0001c0003t0001 | 0/0 | 5362 | 38 | 3 | 2 | 31 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0003t0021 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0003t0023 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0001c0003t0026 | 0/0 | 5409 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5404): Show |
chr18 | 665318 | 717630 |
a0001c0006t0004 | 0/0 | 5353 | 12 | 12 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0013t0002 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0001c0017t0001 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0002c0002t0001 | 0/0 | 5362 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0002c0002t0002 | 0/0 | 5353 | 4 | 0 | 1 | 2 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0002c0002t0004 | 0/0 | 5353 | 18 | 0 | 1 | 14 | 0 | 3 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0002c0002t0005 | 0/1 | 5363 | 17 | 2 | 7 | 0 | 2 | 5 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5358): Show |
chr18 | 665318 | 717630 |
a0002c0002t0006 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0002c0002t0008 | 0/0 | 5362 | 7 | 7 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0002c0002t0009 | 0/0 | 5364 | 6 | 6 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5359): Show |
chr18 | 665318 | 717630 |
a0002c0002t0012 | 0/0 | 5362 | 5 | 5 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0002c0002t0018 | 0/0 | 5353 | 2 | 1 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0002c0002t0020 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5358): Show |
chr18 | 665318 | 717630 |
a0002c0002t0027 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0002c0005t0001 | 0/0 | 5362 | 17 | 0 | 14 | 1 | 1 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0002c0015t0002 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0003c0004t0001 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0003c0004t0002 | 0/0 | 5353 | 2 | 0 | 1 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0003c0004t0003 | 0/0 | 5353 | 35 | 0 | 1 | 33 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0003c0004t0004 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0003c0004t0029 | 0/0 | 5379 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5374): Show |
chr18 | 665318 | 717630 |
a0003c0007t0002 | 0/0 | 5353 | 8 | 1 | 0 | 7 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0003c0007t0003 | 0/0 | 5353 | 3 | 0 | 0 | 3 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0003c0007t0010 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0003c0011t0001 | 0/0 | 5362 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0003c0018t0001 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0004c0008t0001 | 0/0 | 5362 | 3 | 0 | 2 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0004c0008t0004 | 0/0 | 5353 | 4 | 0 | 2 | 0 | 2 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0005c0010t0002 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0005c0010t0025 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5357): Show |
chr18 | 665318 | 717630 |
a0006c0009t0001 | 0/0 | 5021 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5016): Show |
chr18 | 665318 | 717630 |
a0007c0012t0002 | 0/0 | 5353 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
a0008c0014t0022 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5358): Show |
chr18 | 665318 | 717630 |
a0009c0016t0002 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | AGTCC others(5348): Show |
chr18 | 665318 | 717630 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0002 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0007 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0011g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0014g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0015g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0016g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0016g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0017g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0019g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0024g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0028g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0031g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0032g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0033g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0021g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0023g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0026g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0013t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0017t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0018g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0018g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0020g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0027g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0015t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0002g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0029g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0010g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0011t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0011t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0018t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0004g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0005c0010t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0005c0010t0025g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0006c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0006c0009t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0007c0012t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0008c0014t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0009c0016t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00140 | hp2 | a0003 | c0007 | t0010 | g0381 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00280 | hp1 | a0002 | c0005 | t0001 | g0159 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0313 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00323 | hp1 | a0001 | c0001 | t0016 | g0162 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00323 | hp2 | a0007 | c0012 | t0002 | g0165 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00408 | hp2 | a0002 | c0002 | t0004 | g0211 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00423 | hp1 | a0003 | c0004 | t0003 | g0335 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00438 | hp2 | a0003 | c0004 | t0003 | g0377 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00544 | hp2 | a0003 | c0018 | t0001 | g0374 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00609 | hp1 | a0003 | c0007 | t0002 | g0363 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00621 | hp1 | a0002 | c0002 | t0004 | g0145 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00621 | hp2 | a0003 | c0004 | t0003 | g0343 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00642 | hp2 | a0002 | c0005 | t0001 | g0100 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0240 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0272 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00741 | hp2 | a0001 | c0001 | t0010 | g0254 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01069 | hp1 | a0002 | c0002 | t0005 | g0179 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0301 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01070 | hp1 | a0001 | c0001 | t0010 | g0225 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01070 | hp2 | a0002 | c0005 | t0001 | g0160 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0224 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01071 | hp2 | a0002 | c0002 | t0005 | g0178 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01074 | hp2 | a0004 | c0008 | t0004 | g0368 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01081 | hp2 | a0002 | c0005 | t0001 | g0067 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01106 | hp1 | a0002 | c0002 | t0005 | g0213 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0194 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01109 | hp2 | a0001 | c0001 | t0032 | g0296 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01167 | hp1 | a0002 | c0002 | t0018 | g0183 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01175 | hp1 | a0003 | c0004 | t0002 | g0376 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01175 | hp2 | a0002 | c0005 | t0001 | g0099 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01192 | hp1 | a0002 | c0002 | t0020 | g0105 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01256 | hp1 | a0002 | c0002 | t0005 | g0135 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01257 | hp1 | a0002 | c0005 | t0001 | g0011 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01257 | hp2 | a0004 | c0008 | t0001 | g0352 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01258 | hp1 | a0004 | c0008 | t0001 | g0353 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01261 | hp2 | a0003 | c0004 | t0029 | g0348 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0302 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01361 | hp1 | a0002 | c0005 | t0001 | g0044 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01433 | hp1 | a0002 | c0002 | t0005 | g0133 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01433 | hp2 | a0002 | c0002 | t0005 | g0097 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01496 | hp1 | a0002 | c0002 | t0005 | g0177 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01496 | hp2 | a0002 | c0002 | t0004 | g0181 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01515 | hp2 | a0002 | c0002 | t0005 | g0279 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01516 | hp1 | a0004 | c0008 | t0004 | g0019 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01517 | hp1 | a0002 | c0002 | t0005 | g0280 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01517 | hp2 | a0004 | c0008 | t0004 | g0019 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01884 | hp1 | a0002 | c0002 | t0008 | g0108 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01884 | hp2 | a0001 | c0006 | t0004 | g0286 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01891 | hp1 | a0001 | c0006 | t0004 | g0236 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0063 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01928 | hp1 | a0002 | c0005 | t0001 | g0209 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01934 | hp1 | a0002 | c0005 | t0001 | g0176 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01943 | hp2 | a0002 | c0005 | t0001 | g0027 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01978 | hp2 | a0002 | c0005 | t0001 | g0137 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01993 | hp1 | a0004 | c0008 | t0004 | g0382 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0030 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02004 | hp1 | a0003 | c0004 | t0003 | g0371 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02004 | hp2 | a0002 | c0005 | t0001 | g0011 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0215 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02055 | hp2 | a0002 | c0002 | t0009 | g0034 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02056 | hp1 | a0002 | c0005 | t0001 | g0146 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02071 | hp1 | a0002 | c0002 | t0004 | g0141 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02080 | hp2 | a0002 | c0002 | t0004 | g0116 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02083 | hp1 | a0003 | c0004 | t0003 | g0021 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0282 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02132 | hp2 | a0003 | c0004 | t0004 | g0340 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02135 | hp1 | a0003 | c0004 | t0003 | g0331 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02148 | hp1 | a0002 | c0005 | t0001 | g0210 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02155 | hp1 | a0003 | c0004 | t0003 | g0384 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02155 | hp2 | a0002 | c0002 | t0004 | g0138 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02165 | hp2 | a0003 | c0004 | t0003 | g0021 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02257 | hp1 | a0008 | c0014 | t0022 | g0158 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0314 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02258 | hp1 | a0002 | c0002 | t0009 | g0093 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0232 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02300 | hp1 | a0002 | c0005 | t0001 | g0233 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02451 | hp1 | a0001 | c0006 | t0004 | g0004 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02523 | hp2 | a0003 | c0004 | t0003 | g0358 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02572 | hp2 | a0001 | c0006 | t0004 | g0150 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02602 | hp2 | a0002 | c0002 | t0005 | g0102 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02615 | hp1 | a0002 | c0002 | t0009 | g0094 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0320 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02622 | hp1 | a0001 | c0001 | t0017 | g0237 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02630 | hp2 | a0001 | c0006 | t0004 | g0214 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02647 | hp1 | a0001 | c0006 | t0004 | g0004 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02683 | hp1 | a0003 | c0011 | t0001 | g0385 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02683 | hp2 | a0002 | c0002 | t0005 | g0175 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02717 | hp1 | a0001 | c0001 | t0033 | g0109 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02738 | hp2 | a0002 | c0002 | t0005 | g0101 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02809 | hp1 | a0002 | c0002 | t0012 | g0174 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02809 | hp2 | a0002 | c0002 | t0008 | g0107 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02818 | hp1 | a0002 | c0002 | t0008 | g0065 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02886 | hp1 | a0002 | c0002 | t0009 | g0134 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02886 | hp2 | a0001 | c0001 | t0031 | g0319 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0132 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02895 | hp2 | a0003 | c0007 | t0002 | g0337 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02922 | hp1 | a0001 | c0006 | t0004 | g0012 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02976 | hp1 | a0002 | c0002 | t0027 | g0321 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02976 | hp2 | a0002 | c0002 | t0018 | g0185 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03041 | hp2 | a0002 | c0002 | t0012 | g0258 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03130 | hp1 | a0001 | c0006 | t0004 | g0151 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03130 | hp2 | a0001 | c0006 | t0004 | g0238 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03139 | hp1 | a0002 | c0002 | t0012 | g0026 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0207 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03195 | hp1 | a0001 | c0006 | t0004 | g0012 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03209 | hp1 | a0002 | c0002 | t0008 | g0287 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0110 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03225 | hp1 | a0001 | c0001 | t0017 | g0193 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03453 | hp1 | a0002 | c0002 | t0008 | g0153 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0064 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03486 | hp1 | a0002 | c0002 | t0009 | g0098 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03540 | hp1 | a0005 | c0010 | t0025 | g0329 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03540 | hp2 | a0002 | c0002 | t0008 | g0239 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03579 | hp1 | a0001 | c0006 | t0004 | g0004 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0325 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0103 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03704 | hp1 | a0002 | c0005 | t0001 | g0068 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03710 | hp2 | a0003 | c0004 | t0003 | g0357 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03831 | hp1 | a0002 | c0002 | t0005 | g0136 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03831 | hp2 | a0002 | c0002 | t0004 | g0184 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03834 | hp1 | a0003 | c0011 | t0001 | g0386 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03927 | hp1 | a0001 | c0001 | t0030 | g0129 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04115 | hp1 | a0002 | c0002 | t0004 | g0032 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04115 | hp2 | a0001 | c0001 | t0024 | g0291 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04184 | hp2 | a0002 | c0002 | t0004 | g0234 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18522 | hp1 | a0002 | c0002 | t0012 | g0131 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18612 | hp1 | a0003 | c0004 | t0003 | g0366 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18747 | hp1 | a0003 | c0004 | t0003 | g0361 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18747 | hp2 | a0003 | c0004 | t0003 | g0359 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18940 | hp2 | a0003 | c0004 | t0003 | g0334 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0142 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18942 | hp1 | a0003 | c0004 | t0003 | g0365 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18943 | hp1 | a0003 | c0007 | t0003 | g0345 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18945 | hp1 | a0009 | c0016 | t0002 | g0126 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18947 | hp2 | a0001 | c0003 | t0023 | g0246 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18951 | hp1 | a0002 | c0002 | t0004 | g0144 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18951 | hp2 | a0003 | c0004 | t0003 | g0020 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18959 | hp2 | a0003 | c0004 | t0003 | g0355 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18965 | hp1 | a0003 | c0007 | t0002 | g0375 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18965 | hp2 | a0001 | c0001 | t0013 | g0269 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18967 | hp2 | a0006 | c0009 | t0001 | g0275 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0289 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18969 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18971 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18971 | hp2 | a0003 | c0004 | t0003 | g0341 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18972 | hp1 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18973 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18974 | hp1 | a0001 | c0003 | t0026 | g0283 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18975 | hp2 | a0003 | c0004 | t0003 | g0380 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18977 | hp1 | a0001 | c0003 | t0021 | g0271 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18977 | hp2 | a0001 | c0001 | t0015 | g0081 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18978 | hp1 | a0003 | c0004 | t0003 | g0350 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18978 | hp2 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18980 | hp1 | a0003 | c0004 | t0003 | g0333 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0324 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18986 | hp2 | a0003 | c0007 | t0002 | g0364 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18988 | hp1 | a0003 | c0007 | t0002 | g0347 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18993 | hp2 | a0003 | c0007 | t0002 | g0338 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18994 | hp2 | a0003 | c0004 | t0003 | g0349 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18995 | hp2 | a0001 | c0001 | t0014 | g0205 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18998 | hp1 | a0001 | c0001 | t0015 | g0166 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0243 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19002 | hp1 | a0003 | c0004 | t0003 | g0372 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19003 | hp1 | a0001 | c0001 | t0019 | g0022 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19003 | hp2 | a0003 | c0004 | t0003 | g0379 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19004 | hp2 | a0001 | c0001 | t0014 | g0079 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19005 | hp1 | a0001 | c0017 | t0001 | g0328 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19009 | hp1 | a0003 | c0004 | t0003 | g0020 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19011 | hp1 | a0003 | c0004 | t0003 | g0339 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0316 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19030 | hp1 | a0001 | c0001 | t0028 | g0115 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19030 | hp2 | a0002 | c0002 | t0005 | g0187 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19054 | hp2 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19057 | hp1 | a0003 | c0007 | t0003 | g0344 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19058 | hp1 | a0003 | c0004 | t0003 | g0356 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19060 | hp1 | a0001 | c0013 | t0002 | g0148 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19062 | hp1 | a0003 | c0004 | t0001 | g0383 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19063 | hp2 | a0003 | c0004 | t0003 | g0360 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19065 | hp2 | a0003 | c0007 | t0002 | g0346 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19066 | hp1 | a0003 | c0007 | t0003 | g0373 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19066 | hp2 | a0002 | c0002 | t0004 | g0033 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19067 | hp2 | a0003 | c0004 | t0003 | g0369 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19072 | hp2 | a0003 | c0004 | t0003 | g0336 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19077 | hp2 | a0002 | c0002 | t0004 | g0060 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19079 | hp2 | a0003 | c0004 | t0003 | g0370 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19080 | hp2 | a0003 | c0004 | t0003 | g0332 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19082 | hp2 | a0003 | c0004 | t0002 | g0342 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19083 | hp1 | a0003 | c0007 | t0002 | g0362 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19083 | hp2 | a0006 | c0009 | t0001 | g0191 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19086 | hp1 | a0003 | c0004 | t0003 | g0378 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19088 | hp1 | a0001 | c0001 | t0013 | g0152 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19090 | hp1 | a0003 | c0004 | t0003 | g0351 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0295 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19240 | hp2 | a0002 | c0002 | t0006 | g0149 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20129 | hp1 | a0002 | c0002 | t0005 | g0095 | AFR | ASW | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ASW | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20752 | hp2 | a0004 | c0008 | t0001 | g0367 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20905 | hp1 | a0002 | c0002 | t0005 | g0253 | SAS | GIH | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01123 | hp1 | a0001 | c0001 | t0016 | g0071 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0186 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02109 | hp2 | a0001 | c0006 | t0004 | g0304 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02486 | hp1 | a0002 | c0002 | t0008 | g0062 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02559 | hp1 | a0002 | c0015 | t0002 | g0257 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03471 | hp2 | a0005 | c0010 | t0002 | g0330 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG06807 | hp2 | a0002 | c0002 | t0012 | g0091 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18955 | hp2 | a0003 | c0004 | t0003 | g0354 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0227 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0284 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
homoSapiens | chm13v2 | a0002 | c0002 | t0005 | g0106 | REF | REF | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0262 | REF | REF | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:674325 | G | A | 1 | a0008 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1312C>T | p.Leu438Phe | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1355/5362 | 1312/1332 | 438/443 | chr18 | 674325 | |||
chr18:681605 | GTTTAAAT others(9044): Show |
G | 1 | a0006 | 2 | NA18967.hp2 NA19083.hp2 |
exon_loss_variant | HIGH | c.536-25_876+1640del | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/16 | chr18 | 681605 | |||||||
chr18:685988 | G | A | 1 | a0003 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.674C>T | p.Ala225Val | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/16 | 717/5362 | 674/1332 | 225/443 | chr18 | 685988 | |||
chr18:691266 | A | G | 3 | a0002 a0004 a0008 |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
missense_variant | MODERATE | c.434T>C | p.Met145Thr | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 6/16 | 477/5362 | 434/1332 | 145/443 | chr18 | 691266 | |||
chr18:706478 | G | A | 1 | a0009 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.185C>T | p.Thr62Ile | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/16 | 228/5362 | 185/1332 | 62/443 | chr18 | 706478 | |||
chr18:706570 | G | T | 1 | a0007 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.93C>A | p.Asp31Glu | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/16 | 136/5362 | 93/1332 | 31/443 | chr18 | 706570 | |||
chr18:712554 | G | A | 1 | a0005 | 2 | HG03471.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.34C>T | p.Arg12Trp | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 77/5362 | 34/1332 | 12/443 | chr18 | 712554 | |||
chr18:712568 | G | A | 2 | a0003 a0004 |
62 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
missense_variant | MODERATE | c.20C>T | p.Ser7Phe | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 63/5362 | 20/1332 | 7/443 | chr18 | 712568 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:674320 | A | G | 6 | a0001c0003 a0001c0017 a0002c0005 others(3): Show |
64 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
synonymous_variant | LOW | c.1317T>C | p.Pro439Pro | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1360/5362 | 1317/1332 | 439/443 | chr18 | 674320 | |||
chr18:674401 | G | A | 1 | a0002c0015 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1236C>T | p.Pro412Pro | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1279/5362 | 1236/1332 | 412/443 | chr18 | 674401 | |||
chr18:693888 | C | T | 1 | a0001c0006 | 12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.417G>A | p.Val139Val | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/16 | 460/5362 | 417/1332 | 139/443 | chr18 | 693888 | |||
chr18:706558 | C | T | 4 | a0001c0013 a0003c0004 a0003c0018 others(1): Show |
49 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
synonymous_variant | LOW | c.105G>A | p.Ser35Ser | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/16 | 148/5362 | 105/1332 | 35/443 | chr18 | 706558 | |||
chr18:712549 | G | A | 1 | a0001c0017 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.39C>T | p.Asp13Asp | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 82/5362 | 39/1332 | 13/443 | chr18 | 712549 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:670414 | C | T | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3891G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3891 | chr18 | 670414 | ||||||
chr18:670472 | C | T | 1 | a0002c0002t0008 | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3833G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3833 | chr18 | 670472 | ||||||
chr18:670541 | A | G | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3764T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3764 | chr18 | 670541 | ||||||
chr18:670551 | G | A | 1 | a0001c0001t0014 | 2 | NA18995.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3754C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3754 | chr18 | 670551 | ||||||
chr18:670618 | C | T | 2 | a0002c0002t0008 a0002c0002t0027 |
8 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3687G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3687 | chr18 | 670618 | ||||||
chr18:670888 | T | C | 8 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0017 others(5): Show |
59 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3417A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3417 | chr18 | 670888 | ||||||
chr18:670932 | G | C | 1 | a0001c0001t0033 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3373C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3373 | chr18 | 670932 | ||||||
chr18:670995 | A | C | 37 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(34): Show |
265 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*3310T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3310 | chr18 | 670995 | ||||||
chr18:671026 | C | T | 28 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(25): Show |
226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*3279G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3279 | chr18 | 671026 | ||||||
chr18:671050 | T | C | 2 | a0001c0001t0010 a0003c0007t0010 |
6 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3255A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3255 | chr18 | 671050 | ||||||
chr18:671057 | C | T | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3248G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3248 | chr18 | 671057 | ||||||
chr18:671105 | T | C | 24 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0015 others(21): Show |
208 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*3200A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3200 | chr18 | 671105 | ||||||
chr18:671167 | G | A | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3138C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3138 | chr18 | 671167 | ||||||
chr18:671256 | A | G | 1 | a0002c0002t0020 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3049T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3049 | chr18 | 671256 | ||||||
chr18:671293 | C | T | 1 | a0001c0001t0017 | 2 | HG02622.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3012G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3012 | chr18 | 671293 | ||||||
chr18:671520 | C | T | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2785G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2785 | chr18 | 671520 | ||||||
chr18:671648 | A | T | 31 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(28): Show |
230 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2657T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2657 | chr18 | 671648 | ||||||
chr18:671727 | G | A | 26 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0014 others(23): Show |
212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2578C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2578 | chr18 | 671727 | ||||||
chr18:671785 | C | CT | 5 | a0001c0001t0005 a0002c0002t0005 a0002c0002t0012 others(2): Show |
24 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2519dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2519 | chr18 | 671785 | ||||||
chr18:671785 | C | CTT | 1 | a0002c0002t0009 | 6 | HG02055.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2518_*2519dupAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2519 | chr18 | 671785 | ||||||
chr18:671785 | CT | C | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2519delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2519 | chr18 | 671785 | ||||||
chr18:671834 | C | T | 5 | a0001c0001t0005 a0002c0002t0005 a0002c0002t0009 others(2): Show |
29 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2471G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2471 | chr18 | 671834 | ||||||
chr18:671840 | T | C | 2 | a0001c0001t0007 a0001c0001t0019 |
9 | NA18948.hp1 NA18969.hp2 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2465A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2465 | chr18 | 671840 | ||||||
chr18:671977 | A | G | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2328T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2328 | chr18 | 671977 | ||||||
chr18:671988 | C | T | 1 | a0001c0003t0021 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2317G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2317 | chr18 | 671988 | ||||||
chr18:672035 | C | T | 5 | a0001c0001t0005 a0002c0002t0005 a0002c0002t0009 others(2): Show |
29 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2270G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2270 | chr18 | 672035 | ||||||
chr18:672043 | A | G | 35 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(32): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2262T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2262 | chr18 | 672043 | ||||||
chr18:672168 | C | A | 1 | a0001c0001t0015 | 2 | NA18977.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2137G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2137 | chr18 | 672168 | ||||||
chr18:672204 | T | G | 1 | a0005c0010t0025 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2101A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2101 | chr18 | 672204 | ||||||
chr18:672279 | T | TAAAAGTT others(40): Show |
1 | a0001c0003t0026 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2025_*2026insTTTT others(43): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2025 | chr18 | 672279 | ||||||
chr18:672288 | C | T | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2017G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2017 | chr18 | 672288 | ||||||
chr18:672363 | G | A | 32 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(29): Show |
237 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1942 | chr18 | 672363 | ||||||
chr18:672393 | G | GTCTTCAC others(19): Show |
1 | a0003c0004t0029 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1886_*1911dupAGAC others(22): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1911 | chr18 | 672393 | ||||||
chr18:672590 | G | A | 1 | a0001c0001t0016 | 2 | HG00323.hp1 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1715C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1715 | chr18 | 672590 | ||||||
chr18:672595 | G | T | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1710 | chr18 | 672595 | ||||||
chr18:672599 | T | C | 1 | a0001c0001t0031 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1706A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1706 | chr18 | 672599 | ||||||
chr18:672792 | C | T | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1513G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1513 | chr18 | 672792 | ||||||
chr18:672836 | A | G | 5 | a0001c0001t0005 a0002c0002t0005 a0002c0002t0009 others(2): Show |
29 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1469T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1469 | chr18 | 672836 | ||||||
chr18:673016 | C | T | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1289 | chr18 | 673016 | ||||||
chr18:673059 | G | C | 1 | a0001c0001t0032 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1246C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1246 | chr18 | 673059 | ||||||
chr18:673086 | A | G | 18 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0014 others(15): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1219T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1219 | chr18 | 673086 | ||||||
chr18:673211 | G | T | 1 | a0001c0001t0011 | 6 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1094 | chr18 | 673211 | ||||||
chr18:673256 | TG | T | 1 | a0002c0002t0012 | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1048delC | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1048 | chr18 | 673256 | ||||||
chr18:673395 | G | A | 3 | a0001c0001t0006 a0001c0001t0011 a0002c0002t0006 |
16 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*910C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 910 | chr18 | 673395 | ||||||
chr18:673443 | TTTAAAG | T | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*861delCTTTAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 856 | chr18 | 673443 | ||||||
chr18:673613 | A | G | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*692T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 692 | chr18 | 673613 | ||||||
chr18:673710 | G | GT | 7 | a0001c0001t0001 a0001c0001t0005 a0001c0003t0001 others(4): Show |
12 | HG00544.hp2 HG01192.hp2 HG02738.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*594dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 594 | chr18 | 673710 | ||||||
chr18:673710 | GTTT | G | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(26): Show |
224 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*592_*594delAAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 592 | chr18 | 673710 | ||||||
chr18:673732 | CTT | C | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*571_*572delAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 571 | chr18 | 673732 | ||||||
chr18:673789 | A | G | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*516T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 516 | chr18 | 673789 | ||||||
chr18:673995 | T | C | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*310A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 310 | chr18 | 673995 | ||||||
chr18:674012 | T | G | 30 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(27): Show |
229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*293A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 293 | chr18 | 674012 | ||||||
chr18:712590 | C | T | 1 | a0001c0001t0019 | 1 | NA19003.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 3 | chr18 | 712590 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:674440 | A | C | 197 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(194): Show |
212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1231-34T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674440 | |||||||
chr18:674535 | T | C | 235 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(232): Show |
250 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1231-129A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674535 | |||||||
chr18:674579 | C | T | 19 | a0001c0003t0001g0030 a0001c0003t0001g0250 a0001c0003t0001g0272 others(16): Show |
20 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-173G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674579 | |||||||
chr18:674645 | T | C | 213 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(210): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1231-239A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674645 | |||||||
chr18:674693 | T | C | 1 | a0002c0002t0004g0060 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1231-287A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674693 | |||||||
chr18:674744 | A | C | 1 | a0001c0003t0001g0325 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1231-338T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674744 | |||||||
chr18:674852 | C | T | 16 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(13): Show |
16 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1231-446G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674852 | |||||||
chr18:675000 | C | T | 212 | a0001c0001t0001g0310 a0001c0001t0002g0002 a0001c0001t0002g0006 others(209): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1230+321G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675000 | |||||||
chr18:675007 | T | C | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1230+314A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675007 | |||||||
chr18:675272 | C | T | 20 | a0001c0001t0002g0039 a0001c0001t0006g0048 a0001c0001t0006g0111 others(17): Show |
20 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.1230+49G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675272 | |||||||
chr18:675300 | G | T | 1 | a0002c0002t0004g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1230+21C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675300 | |||||||
chr18:675307 | A | G | 54 | a0001c0001t0001g0327 a0001c0001t0002g0076 a0001c0001t0002g0198 others(51): Show |
55 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1230+14T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675307 | |||||||
chr18:675643 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1149-241A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675643 | |||||||
chr18:675774 | T | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-372A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675774 | |||||||
chr18:675787 | C | T | 289 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0001g0059 others(286): Show |
306 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1149-385G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675787 | |||||||
chr18:675789 | T | C | 39 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1149-387A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675789 | |||||||
chr18:675816 | G | A | 1 | a0001c0003t0001g0277 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1149-414C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675816 | |||||||
chr18:675821 | T | TAA | 161 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-420_1149-419i others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675821 | |||||||
chr18:675822 | T | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-420A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675822 | |||||||
chr18:675823 | T | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-421A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675823 | |||||||
chr18:675824 | T | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-422A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675824 | |||||||
chr18:675825 | G | A | 161 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-423C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675825 | |||||||
chr18:675903 | C | T | 159 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(156): Show |
172 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1149-501G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675903 | |||||||
chr18:676008 | G | C | 267 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(264): Show |
283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1149-606C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676008 | |||||||
chr18:676030 | A | G | 3 | a0001c0003t0001g0325 a0003c0011t0001g0385 a0003c0011t0001g0386 |
3 | HG02683.hp1 HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1149-628T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676030 | |||||||
chr18:676059 | A | T | 8 | a0002c0002t0008g0062 a0002c0002t0008g0065 a0002c0002t0008g0107 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-657T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676059 | |||||||
chr18:676139 | T | G | 1 | a0001c0001t0002g0290 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1149-737A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676139 | |||||||
chr18:676228 | T | A | 64 | a0001c0001t0005g0288 a0001c0001t0006g0048 a0001c0001t0006g0111 others(61): Show |
65 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1149-826A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676228 | |||||||
chr18:676293 | T | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0167 |
2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1149-891A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676293 | |||||||
chr18:676329 | G | C | 2 | a0001c0001t0017g0193 a0001c0001t0017g0237 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1149-927C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676329 | |||||||
chr18:676331 | G | C | 63 | a0001c0001t0005g0288 a0001c0001t0006g0048 a0001c0001t0006g0111 others(60): Show |
64 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1149-929C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676331 | |||||||
chr18:676403 | T | TTC | 160 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1148+940_1148+941d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676403 | |||||||
chr18:676473 | C | T | 68 | a0001c0001t0005g0288 a0001c0001t0006g0048 a0001c0001t0006g0111 others(65): Show |
72 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.1148+872G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676473 | |||||||
chr18:676490 | G | C | 60 | a0001c0001t0005g0288 a0001c0001t0006g0048 a0001c0001t0006g0111 others(57): Show |
61 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1148+855C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676490 | |||||||
chr18:676518 | T | C | 162 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(159): Show |
175 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1148+827A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676518 | |||||||
chr18:676711 | C | A | 1 | a0001c0001t0006g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1148+634G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676711 | |||||||
chr18:676789 | A | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0009 others(66): Show |
76 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.1148+556T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676789 | |||||||
chr18:676924 | G | T | 1 | a0002c0002t0005g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1148+421C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676924 | |||||||
chr18:676940 | T | C | 1 | a0003c0004t0003g0351 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1148+405A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676940 | |||||||
chr18:677214 | G | A | 160 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1148+131C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 677214 | |||||||
chr18:677240 | G | A | 161 | a0001c0001t0001g0216 a0001c0001t0002g0002 a0001c0001t0002g0006 others(158): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1148+105C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 677240 | |||||||
chr18:677302 | G | A | 160 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1148+43C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 677302 | |||||||
chr18:677452 | G | A | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.1049-8C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677452 | |||||||
chr18:677621 | T | G | 22 | a0002c0002t0004g0008 a0002c0002t0004g0032 a0002c0002t0004g0033 others(19): Show |
24 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1048+122A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677621 | |||||||
chr18:677677 | A | G | 2 | a0002c0002t0009g0093 a0002c0002t0009g0094 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1048+66T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677677 | |||||||
chr18:677736 | C | T | 1 | a0001c0001t0032g0296 | 1 | HG01109.hp2 | splice_region_variant&intron_variant | LOW | c.1048+7G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677736 | |||||||
chr18:677737 | G | A | 1 | a0001c0003t0023g0246 | 1 | NA18947.hp2 | splice_region_variant&intron_variant | LOW | c.1048+6C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677737 | |||||||
chr18:677931 | C | G | 128 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(125): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.919-59G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677931 | |||||||
chr18:677944 | C | T | 1 | a0008c0014t0022g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-72G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677944 | |||||||
chr18:677970 | T | G | 13 | a0001c0001t0002g0036 a0001c0001t0002g0050 a0001c0001t0002g0051 others(10): Show |
13 | HG01106.hp2 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.919-98A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677970 | |||||||
chr18:677992 | C | A | 1 | a0002c0002t0005g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919-120G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677992 | |||||||
chr18:678124 | G | A | 1 | a0008c0014t0022g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-252C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678124 | |||||||
chr18:678135 | G | A | 1 | a0002c0002t0005g0213 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.919-263C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678135 | |||||||
chr18:678158 | A | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0255 a0001c0001t0001g0281 others(1): Show |
4 | HG00639.hp2 HG01261.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-286T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678158 | |||||||
chr18:678235 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919-363G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678235 | |||||||
chr18:678481 | C | T | 160 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(157): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.918+215G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678481 | |||||||
chr18:678499 | T | C | 6 | a0001c0001t0002g0035 a0001c0001t0002g0040 a0001c0001t0002g0055 others(3): Show |
6 | NA18941.hp1 NA18984.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+197A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678499 | |||||||
chr18:678666 | C | T | 1 | a0001c0003t0001g0324 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.918+30G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678666 | |||||||
chr18:678847 | T | C | 40 | a0001c0001t0005g0288 a0001c0003t0001g0272 a0002c0002t0005g0095 others(37): Show |
41 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.877-110A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 678847 | |||||||
chr18:678929 | G | A | 1 | a0003c0004t0003g0331 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.877-192C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 678929 | |||||||
chr18:678947 | A | G | 271 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(268): Show |
287 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.877-210T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 678947 | |||||||
chr18:679001 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.877-264C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679001 | |||||||
chr18:679031 | G | A | 8 | a0002c0002t0008g0062 a0002c0002t0008g0065 a0002c0002t0008g0107 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.877-294C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679031 | |||||||
chr18:679042 | C | T | 5 | a0001c0003t0001g0240 a0001c0003t0001g0250 a0001c0003t0001g0260 others(2): Show |
5 | HG00673.hp2 HG02040.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-305G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679042 | |||||||
chr18:679067 | A | G | 1 | a0001c0001t0031g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.877-330T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679067 | |||||||
chr18:679150 | C | T | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-413G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679150 | |||||||
chr18:679199 | CTCTCA | C | 10 | a0001c0001t0001g0219 a0001c0001t0001g0252 a0001c0001t0001g0270 others(7): Show |
10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.877-467_877-463del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679199 | |||||||
chr18:679202 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.877-465A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679202 | |||||||
chr18:679208 | C | CT | 64 | a0001c0001t0001g0312 a0001c0001t0005g0288 a0001c0001t0007g0218 others(61): Show |
65 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.877-472dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | |||||||
chr18:679208 | CT | C | 11 | a0001c0001t0001g0261 a0001c0001t0002g0031 a0001c0001t0002g0040 others(8): Show |
13 | HG00408.hp1 HG01070.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.877-472delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | |||||||
chr18:679208 | CTT | C | 149 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(146): Show |
160 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.877-473_877-472del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | |||||||
chr18:679208 | CTTT | C | 9 | a0001c0001t0002g0120 a0001c0001t0002g0204 a0001c0003t0001g0274 others(6): Show |
9 | NA18967.hp2 NA18977.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.877-474_877-472del others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | |||||||
chr18:679300 | C | G | 6 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0063 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-563G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679300 | |||||||
chr18:679334 | T | C | 271 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(268): Show |
287 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.877-597A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679334 | |||||||
chr18:679335 | G | A | 1 | a0009c0016t0002g0126 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.877-598C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679335 | |||||||
chr18:679353 | G | A | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.877-616C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679353 | |||||||
chr18:679375 | A | AT | 40 | a0001c0001t0005g0288 a0001c0003t0001g0272 a0002c0002t0005g0095 others(37): Show |
41 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.877-639dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679375 | |||||||
chr18:679398 | A | G | 40 | a0001c0001t0005g0288 a0001c0003t0001g0272 a0002c0002t0005g0095 others(37): Show |
41 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.877-661T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679398 | |||||||
chr18:679449 | T | TCC | 168 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(165): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.877-714_877-713dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679449 | |||||||
chr18:679561 | GA | G | 201 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0028 others(198): Show |
210 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.877-825delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679561 | |||||||
chr18:679561 | GAA | G | 68 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0009 others(65): Show |
75 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.877-826_877-825del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679561 | |||||||
chr18:679626 | G | T | 1 | a0001c0003t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.877-889C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679626 | |||||||
chr18:679637 | T | C | 61 | a0001c0001t0005g0288 a0001c0001t0011g0046 a0001c0001t0011g0047 others(58): Show |
62 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.877-900A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679637 | |||||||
chr18:679653 | G | C | 40 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(37): Show |
42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.877-916C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679653 | |||||||
chr18:679660 | C | G | 70 | a0001c0001t0005g0288 a0001c0001t0006g0048 a0001c0001t0006g0111 others(67): Show |
71 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.877-923G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679660 | |||||||
chr18:679769 | C | G | 1 | a0001c0001t0033g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.877-1032G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679769 | |||||||
chr18:679878 | C | T | 40 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(37): Show |
42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.877-1141G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679878 | |||||||
chr18:679990 | T | TA | 9 | a0001c0001t0033g0109 a0002c0002t0008g0062 a0002c0002t0008g0065 others(6): Show |
9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.877-1254dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679990 | |||||||
chr18:680312 | T | C | 40 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(37): Show |
42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.877-1575A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680312 | |||||||
chr18:680373 | G | A | 1 | a0001c0001t0011g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.877-1636C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680373 | |||||||
chr18:680380 | C | T | 177 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(174): Show |
190 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.877-1643G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680380 | |||||||
chr18:680520 | A | C | 137 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(134): Show |
148 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.877-1783T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680520 | |||||||
chr18:680590 | A | G | 2 | a0001c0003t0001g0260 a0001c0003t0001g0289 |
2 | NA18961.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.877-1853T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680590 | |||||||
chr18:680676 | G | GT | 7 | a0001c0001t0007g0222 a0001c0001t0024g0291 a0001c0003t0001g0273 others(4): Show |
7 | HG02698.hp1 HG04115.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.877-1940dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680676 | |||||||
chr18:680676 | GT | G | 68 | a0001c0001t0001g0265 a0001c0001t0005g0288 a0001c0001t0006g0156 others(65): Show |
69 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.877-1940delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680676 | |||||||
chr18:680676 | GTT | G | 199 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(196): Show |
214 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.877-1941_877-1940d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680676 | |||||||
chr18:680685 | T | G | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-1948A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680685 | |||||||
chr18:680687 | T | G | 22 | a0002c0002t0004g0008 a0002c0002t0004g0032 a0002c0002t0004g0033 others(19): Show |
24 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.877-1950A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680687 | |||||||
chr18:680742 | G | A | 1 | a0001c0003t0026g0283 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.877-2005C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680742 | |||||||
chr18:680838 | G | A | 176 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(173): Show |
189 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.877-2101C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680838 | |||||||
chr18:680985 | T | C | 68 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0009 others(65): Show |
75 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.877-2248A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680985 | |||||||
chr18:681047 | A | T | 40 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(37): Show |
42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.876+2199T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681047 | |||||||
chr18:681051 | G | A | 1 | a0002c0002t0005g0135 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.876+2195C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681051 | |||||||
chr18:681077 | G | C | 9 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(6): Show |
9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+2169C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681077 | |||||||
chr18:681145 | AGCCACTA others(6): Show |
A | 1 | a0007c0012t0002g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.876+2088_876+2100d others(15): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681145 | |||||||
chr18:681192 | G | A | 383 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(380): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.876+2054C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681192 | |||||||
chr18:681267 | T | G | 9 | a0001c0006t0004g0004 a0001c0006t0004g0012 a0001c0006t0004g0150 others(6): Show |
12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.876+1979A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681267 | |||||||
chr18:681469 | C | T | 1 | a0001c0001t0032g0296 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.876+1777G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681469 | |||||||
chr18:681624 | T | C | 1 | a0003c0004t0002g0342 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.876+1622A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681624 | |||||||
chr18:681724 | C | T | 53 | a0001c0001t0005g0288 a0001c0001t0011g0046 a0001c0001t0011g0047 others(50): Show |
54 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.876+1522G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681724 | |||||||
chr18:681779 | A | G | 1 | a0008c0014t0022g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.876+1467T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681779 | |||||||
chr18:681823 | G | A | 38 | a0003c0004t0001g0383 a0003c0004t0003g0020 a0003c0004t0003g0021 others(35): Show |
40 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.876+1423C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681823 | |||||||
chr18:681927 | T | C | 1 | a0002c0002t0004g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.876+1319A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681927 | |||||||
chr18:681962 | G | A | 159 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(156): Show |
172 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.876+1284C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681962 | |||||||
chr18:682260 | C | T | 1 | a0001c0001t0033g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.876+986G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682260 | |||||||
chr18:682399 | C | T | 12 | a0001c0001t0005g0288 a0002c0002t0002g0103 a0002c0002t0005g0095 others(9): Show |
12 | HG01106.hp1 HG01192.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.876+847G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682399 | |||||||
chr18:682411 | A | G | 1 | a0001c0003t0001g0274 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.876+835T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682411 | |||||||
chr18:682466 | A | G | 1 | a0003c0007t0002g0347 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.876+780T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682466 | |||||||
chr18:682470 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876+776A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682470 | |||||||
chr18:682715 | C | CA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0147 a0001c0001t0001g0212 others(35): Show |
41 | HG00597.hp2 HG01123.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.876+530dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682715 | |||||||
chr18:682715 | C | CAA | 10 | a0001c0006t0004g0150 a0002c0002t0008g0062 a0002c0002t0008g0065 others(7): Show |
10 | HG01884.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.876+529_876+530dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682715 | |||||||
chr18:682715 | C | CAAA | 34 | a0001c0001t0017g0193 a0003c0004t0001g0383 a0003c0004t0003g0020 others(31): Show |
36 | HG00423.hp1 HG00621.hp2 HG02004.hp1 others(33): Show |
intron_variant | MODIFIER | c.876+528_876+530dup others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682715 | |||||||
chr18:682723 | A | AT | 9 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(6): Show |
9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+522_876+523ins others(1): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682723 | |||||||
chr18:682881 | TCAAAA | T | 103 | a0001c0001t0005g0288 a0001c0001t0006g0048 a0001c0001t0006g0111 others(100): Show |
106 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.876+360_876+364del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682881 | |||||||
chr18:682922 | C | CA | 72 | a0001c0001t0001g0259 a0001c0001t0017g0193 a0001c0003t0001g0272 others(69): Show |
75 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.876+323dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682922 | |||||||
chr18:682922 | C | CAA | 18 | a0001c0001t0005g0288 a0001c0001t0017g0237 a0002c0002t0002g0103 others(15): Show |
18 | HG01106.hp1 HG01192.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.876+322_876+323dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682922 | |||||||
chr18:682922 | CA | C | 9 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(6): Show |
9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+323delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682922 | |||||||
chr18:682925 | A | AC | 7 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0063 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+320_876+321ins others(1): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682925 | |||||||
chr18:682926 | A | C | 9 | a0001c0001t0001g0266 a0002c0002t0008g0062 a0002c0002t0008g0065 others(6): Show |
9 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+320T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682926 | |||||||
chr18:682941 | C | T | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+305G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682941 | |||||||
chr18:683001 | C | A | 1 | a0008c0014t0022g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.876+245G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683001 | |||||||
chr18:683094 | C | G | 54 | a0001c0001t0005g0288 a0001c0001t0011g0046 a0001c0001t0011g0047 others(51): Show |
55 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.876+152G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683094 | |||||||
chr18:683116 | C | G | 41 | a0001c0001t0005g0288 a0001c0003t0001g0272 a0002c0002t0002g0103 others(38): Show |
42 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.876+130G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683116 | |||||||
chr18:683126 | A | G | 3 | a0002c0002t0004g0008 a0002c0002t0004g0045 a0002c0002t0004g0142 |
3 | NA18941.hp2 NA18949.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.876+120T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683126 | |||||||
chr18:683440 | C | T | 40 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(37): Show |
42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.742-60G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683440 | |||||||
chr18:683441 | G | A | 136 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(133): Show |
147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.742-61C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683441 | |||||||
chr18:683452 | A | G | 9 | a0001c0006t0004g0004 a0001c0006t0004g0012 a0001c0006t0004g0150 others(6): Show |
12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-72T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683452 | |||||||
chr18:683525 | G | A | 1 | a0001c0001t0011g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742-145C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683525 | |||||||
chr18:683573 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742-193C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683573 | |||||||
chr18:683607 | C | T | 271 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(268): Show |
287 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.742-227G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683607 | |||||||
chr18:683664 | C | T | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.742-284G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683664 | |||||||
chr18:683732 | G | A | 1 | a0001c0001t0033g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742-352C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683732 | |||||||
chr18:683766 | A | ACATTGTT others(1): Show |
24 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0031 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.742-387_742-386ins others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683766 | |||||||
chr18:683767 | A | G | 24 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0031 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.742-387T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683767 | |||||||
chr18:683861 | T | C | 40 | a0001c0001t0005g0288 a0001c0003t0001g0272 a0002c0002t0002g0103 others(37): Show |
41 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.742-481A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683861 | |||||||
chr18:683901 | T | C | 9 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(6): Show |
9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.742-521A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683901 | |||||||
chr18:683919 | A | G | 1 | a0002c0002t0027g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.742-539T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683919 | |||||||
chr18:683984 | ATTTCT | A | 11 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(8): Show |
11 | HG02257.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.742-609_742-605del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683984 | |||||||
chr18:683999 | CT | C | 73 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0063 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.742-620delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683999 | |||||||
chr18:683999 | CTT | C | 9 | a0001c0001t0017g0193 a0003c0004t0003g0021 a0003c0004t0003g0332 others(6): Show |
10 | HG00438.hp2 HG00621.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-621_742-620del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683999 | |||||||
chr18:684025 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742-645C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684025 | |||||||
chr18:684048 | C | T | 115 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0001t0002g0002 others(112): Show |
123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.742-668G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684048 | |||||||
chr18:684063 | G | A | 1 | a0003c0004t0029g0348 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.742-683C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684063 | |||||||
chr18:684112 | G | A | 1 | a0002c0005t0001g0027 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.742-732C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684112 | |||||||
chr18:684139 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.742-759C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684139 | |||||||
chr18:684177 | A | G | 6 | a0002c0002t0008g0062 a0002c0002t0008g0107 a0002c0002t0008g0108 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.742-797T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684177 | |||||||
chr18:684185 | C | T | 1 | a0002c0002t0004g0184 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.742-805G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684185 | |||||||
chr18:684197 | A | G | 11 | a0002c0002t0002g0103 a0002c0002t0004g0184 a0002c0002t0005g0095 others(8): Show |
11 | HG01106.hp1 HG01433.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.742-817T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684197 | |||||||
chr18:684217 | A | C | 1 | a0001c0001t0024g0291 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.742-837T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684217 | |||||||
chr18:684287 | A | G | 90 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0063 others(87): Show |
95 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.742-907T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684287 | |||||||
chr18:684335 | C | T | 43 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0003c0004t0001g0383 others(40): Show |
45 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.742-955G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684335 | |||||||
chr18:684371 | T | C | 1 | a0002c0002t0006g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.742-991A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684371 | |||||||
chr18:684373 | C | T | 1 | a0001c0001t0031g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.742-993G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684373 | |||||||
chr18:684523 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.742-1143A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684523 | |||||||
chr18:684570 | C | T | 13 | a0001c0001t0011g0046 a0001c0001t0011g0047 a0001c0001t0011g0063 others(10): Show |
13 | HG01109.hp1 HG01192.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.742-1190G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684570 | |||||||
chr18:684766 | T | C | 285 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(282): Show |
299 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.741+1155A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684766 | |||||||
chr18:684846 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.741+1075T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684846 | |||||||
chr18:684864 | AT | A | 80 | a0001c0001t0001g0015 a0001c0001t0001g0263 a0001c0001t0001g0266 others(77): Show |
81 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.741+1056delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684864 | |||||||
chr18:684993 | G | A | 1 | a0001c0001t0006g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.741+928C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684993 | |||||||
chr18:685026 | A | AT | 363 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(360): Show |
394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.741+894dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685026 | |||||||
chr18:685075 | G | A | 7 | a0002c0002t0008g0062 a0002c0002t0008g0065 a0002c0002t0008g0107 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.741+846C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685075 | |||||||
chr18:685158 | G | C | 64 | a0001c0001t0006g0226 a0001c0001t0011g0046 a0001c0001t0011g0047 others(61): Show |
65 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.741+763C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685158 | |||||||
chr18:685165 | CT | C | 13 | a0002c0002t0001g0104 a0002c0005t0001g0011 a0002c0005t0001g0027 others(10): Show |
14 | HG00642.hp2 HG01123.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.741+755delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685165 | |||||||
chr18:685198 | G | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0318 |
2 | HG00597.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.741+723C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685198 | |||||||
chr18:685239 | C | T | 5 | a0001c0001t0001g0318 a0001c0001t0011g0046 a0001c0001t0011g0047 others(2): Show |
5 | HG00597.hp2 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+682G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685239 | |||||||
chr18:685340 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.741+581A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685340 | |||||||
chr18:685392 | T | C | 2 | a0001c0001t0017g0193 a0001c0001t0017g0237 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.741+529A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685392 | |||||||
chr18:685447 | A | G | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.741+474T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685447 | |||||||
chr18:685511 | T | C | 51 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(48): Show |
52 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.741+410A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685511 | |||||||
chr18:685574 | T | G | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.741+347A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685574 | |||||||
chr18:685627 | CAT | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.741+292_741+293del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685627 | |||||||
chr18:685671 | G | A | 1 | a0001c0001t0006g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.741+250C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685671 | |||||||
chr18:685692 | A | C | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+229T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685692 | |||||||
chr18:685706 | C | G | 2 | a0002c0002t0005g0279 a0002c0002t0005g0280 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.741+215G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685706 | |||||||
chr18:685783 | G | A | 4 | a0001c0001t0002g0066 a0001c0001t0002g0195 a0001c0001t0002g0196 others(1): Show |
4 | HG03017.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+138C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685783 | |||||||
chr18:685797 | C | T | 273 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(270): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.741+124G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685797 | |||||||
chr18:685799 | C | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.741+122G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685799 | |||||||
chr18:685818 | A | G | 42 | a0001c0013t0002g0148 a0003c0004t0001g0383 a0003c0004t0002g0376 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.741+103T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685818 | |||||||
chr18:685861 | G | A | 2 | a0002c0002t0009g0098 a0002c0002t0009g0134 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.741+60C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685861 | |||||||
chr18:686055 | G | A | 1 | a0001c0003t0001g0013 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.654-47C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686055 | |||||||
chr18:686151 | A | T | 1 | a0001c0001t0002g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.654-143T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686151 | |||||||
chr18:686289 | C | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.654-281G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686289 | |||||||
chr18:686370 | A | G | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-362T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686370 | |||||||
chr18:686386 | G | T | 2 | a0001c0001t0017g0193 a0001c0001t0017g0237 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.654-378C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686386 | |||||||
chr18:686662 | C | T | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-654G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686662 | |||||||
chr18:686669 | T | C | 1 | a0005c0010t0025g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.654-661A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686669 | |||||||
chr18:686738 | C | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.654-730G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686738 | |||||||
chr18:686782 | C | T | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-774G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686782 | |||||||
chr18:686788 | G | C | 1 | a0002c0005t0001g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.654-780C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686788 | |||||||
chr18:686807 | C | T | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-799G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686807 | |||||||
chr18:686858 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.654-850C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686858 | |||||||
chr18:687009 | CAGAT | C | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-1005_654-1002d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687009 | |||||||
chr18:687017 | C | T | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-1009G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687017 | |||||||
chr18:687031 | C | T | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.654-1023G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687031 | |||||||
chr18:687045 | G | A | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-1037C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687045 | |||||||
chr18:687055 | A | ACAGC | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-1051_654-1048d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687055 | |||||||
chr18:687056 | C | T | 3 | a0001c0001t0006g0048 a0001c0001t0006g0156 a0001c0001t0006g0157 |
3 | HG02630.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.654-1048G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687056 | |||||||
chr18:687119 | G | T | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-1111C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687119 | |||||||
chr18:687192 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.654-1184G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687192 | |||||||
chr18:687208 | C | G | 53 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0002c0002t0001g0096 others(50): Show |
54 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-1200G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687208 | |||||||
chr18:687223 | G | A | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.654-1215C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687223 | |||||||
chr18:687261 | T | A | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-1253A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687261 | |||||||
chr18:687267 | C | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.654-1259G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687267 | |||||||
chr18:687270 | G | A | 48 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(45): Show |
49 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.654-1262C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687270 | |||||||
chr18:687410 | C | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.653+1164G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687410 | |||||||
chr18:687534 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.653+1040C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687534 | |||||||
chr18:687850 | G | A | 2 | a0001c0001t0017g0193 a0001c0001t0017g0237 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.653+724C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687850 | |||||||
chr18:687879 | C | T | 1 | a0007c0012t0002g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.653+695G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687879 | |||||||
chr18:687904 | C | A | 57 | a0001c0006t0004g0151 a0002c0002t0001g0096 a0002c0002t0001g0104 others(54): Show |
58 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.653+670G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687904 | |||||||
chr18:687914 | C | G | 2 | a0002c0002t0009g0034 a0008c0014t0022g0158 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.653+660G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687914 | |||||||
chr18:688012 | C | T | 1 | a0001c0001t0002g0006 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.653+562G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688012 | |||||||
chr18:688040 | G | A | 1 | a0002c0005t0001g0210 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.653+534C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688040 | |||||||
chr18:688103 | C | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(319): Show |
345 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.653+471G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688103 | |||||||
chr18:688123 | C | T | 8 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.653+451G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688123 | |||||||
chr18:688139 | T | C | 42 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(39): Show |
43 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.653+435A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688139 | |||||||
chr18:688167 | C | CA | 104 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0028 others(101): Show |
110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.653+406dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688167 | |||||||
chr18:688167 | C | CAA | 120 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(117): Show |
129 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+405_653+406dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688167 | |||||||
chr18:688167 | C | CAAA | 6 | a0002c0002t0005g0178 a0002c0002t0005g0179 a0002c0005t0001g0067 others(3): Show |
6 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+404_653+406dup others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688167 | |||||||
chr18:688190 | G | T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0229 |
2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.653+384C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688190 | |||||||
chr18:688191 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.653+383T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688191 | |||||||
chr18:688428 | G | A | 85 | a0001c0001t0017g0193 a0001c0001t0017g0237 a0002c0002t0001g0096 others(82): Show |
88 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.653+146C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688428 | |||||||
chr18:688441 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+133A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688441 | |||||||
chr18:688442 | A | C | 1 | a0002c0002t0004g0184 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.653+132T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688442 | |||||||
chr18:688463 | G | T | 272 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(269): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.653+111C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688463 | |||||||
chr18:688711 | T | C | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-103A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 688711 | |||||||
chr18:689018 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.619-410C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689018 | |||||||
chr18:689021 | T | G | 1 | a0002c0002t0009g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.619-413A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689021 | |||||||
chr18:689070 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.619-462A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689070 | |||||||
chr18:689142 | C | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.619-534G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689142 | |||||||
chr18:689232 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.619-624G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689232 | |||||||
chr18:689242 | G | C | 125 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(122): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.619-634C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689242 | |||||||
chr18:689333 | G | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.619-725C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689333 | |||||||
chr18:689437 | C | T | 8 | a0002c0002t0002g0103 a0002c0002t0005g0097 a0002c0002t0005g0101 others(5): Show |
8 | HG01256.hp1 HG01433.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.619-829G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689437 | |||||||
chr18:689660 | G | T | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+889C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689660 | |||||||
chr18:689665 | A | G | 25 | a0002c0002t0002g0303 a0002c0002t0004g0008 a0002c0002t0004g0032 others(22): Show |
27 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.618+884T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689665 | |||||||
chr18:689680 | TCTGCCCC others(5): Show |
T | 1 | a0001c0001t0017g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618+857_618+868del others(12): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689680 | |||||||
chr18:689693 | C | T | 1 | a0001c0001t0032g0296 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618+856G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689693 | |||||||
chr18:689748 | CTGAG | C | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+797_618+800del others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689748 | |||||||
chr18:689779 | C | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.618+770G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689779 | |||||||
chr18:689818 | C | T | 170 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0088 others(167): Show |
183 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.618+731G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689818 | |||||||
chr18:689843 | A | G | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+706T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689843 | |||||||
chr18:689845 | AGGCATGA others(486): Show |
A | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+211_618+703del | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689845 | |||||||
chr18:689854 | T | G | 131 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(128): Show |
142 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.618+695A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689854 | |||||||
chr18:690207 | G | A | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+342C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690207 | |||||||
chr18:690230 | T | G | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.618+319A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690230 | |||||||
chr18:690297 | T | C | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.618+252A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690297 | |||||||
chr18:690339 | T | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+210A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690339 | |||||||
chr18:690346 | T | C | 1 | a0001c0001t0033g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.618+203A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690346 | |||||||
chr18:690436 | C | T | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.618+113G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690436 | |||||||
chr18:690460 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.618+89C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690460 | |||||||
chr18:690521 | G | A | 1 | a0003c0007t0002g0337 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.618+28C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690521 | |||||||
chr18:690656 | A | G | 7 | a0002c0002t0008g0062 a0002c0002t0008g0065 a0002c0002t0008g0107 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-25T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690656 | |||||||
chr18:690702 | A | AAGCTGTT others(15): Show |
168 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(165): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.536-93_536-72dupGG others(20): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690702 | |||||||
chr18:690702 | A | AAGCTGTT others(37): Show |
1 | a0001c0001t0002g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.536-72_536-71insGG others(42): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690702 | |||||||
chr18:690734 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0180 |
2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.536-103G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690734 | |||||||
chr18:690781 | G | A | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-150C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690781 | |||||||
chr18:690810 | C | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.536-179G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690810 | |||||||
chr18:691117 | T | C | 2 | a0001c0003t0001g0273 a0001c0003t0001g0298 |
2 | NA18968.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.497-11A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 6/15 | chr18 | 691117 | |||||||
chr18:691173 | G | A | 272 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(269): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.496+31C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 6/15 | chr18 | 691173 | |||||||
chr18:691305 | C | G | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-29G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691305 | |||||||
chr18:691439 | T | C | 274 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(271): Show |
290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.424-163A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691439 | |||||||
chr18:691484 | T | A | 1 | a0002c0002t0002g0192 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424-208A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691484 | |||||||
chr18:691485 | C | G | 1 | a0002c0002t0002g0192 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424-209G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691485 | |||||||
chr18:691507 | G | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.424-231C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691507 | |||||||
chr18:691682 | T | A | 1 | a0001c0001t0017g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.424-406A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691682 | |||||||
chr18:691780 | A | G | 94 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(91): Show |
97 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.424-504T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691780 | |||||||
chr18:691890 | T | C | 91 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(88): Show |
94 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.424-614A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691890 | |||||||
chr18:691927 | C | T | 14 | a0002c0002t0006g0149 a0002c0002t0008g0062 a0002c0002t0008g0065 others(11): Show |
14 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.424-651G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691927 | |||||||
chr18:691968 | A | G | 1 | a0003c0004t0003g0370 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.424-692T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691968 | |||||||
chr18:692066 | C | A | 4 | a0002c0002t0002g0103 a0002c0002t0005g0101 a0002c0002t0005g0136 others(1): Show |
4 | HG01496.hp1 HG02738.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-790G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692066 | |||||||
chr18:692082 | G | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.424-806C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692082 | |||||||
chr18:692095 | A | G | 272 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(269): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.424-819T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692095 | |||||||
chr18:692107 | T | C | 124 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(121): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.424-831A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692107 | |||||||
chr18:692118 | T | C | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.424-842A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692118 | |||||||
chr18:692152 | T | C | 80 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(77): Show |
83 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.424-876A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692152 | |||||||
chr18:692154 | C | T | 1 | a0003c0007t0002g0362 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424-878G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692154 | |||||||
chr18:692183 | C | T | 115 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(112): Show |
123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.424-907G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692183 | |||||||
chr18:692233 | T | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.424-957A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692233 | |||||||
chr18:692238 | T | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.424-962A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692238 | |||||||
chr18:692251 | A | G | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-975T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692251 | |||||||
chr18:692282 | T | G | 169 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(166): Show |
182 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.424-1006A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692282 | |||||||
chr18:692397 | C | T | 2 | a0001c0001t0010g0301 a0003c0007t0010g0381 |
2 | HG00140.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.424-1121G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692397 | |||||||
chr18:692517 | A | G | 1 | a0001c0001t0031g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.424-1241T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692517 | |||||||
chr18:692596 | T | TA | 28 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(25): Show |
29 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.423+1285dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692596 | |||||||
chr18:692596 | TA | T | 15 | a0001c0001t0001g0244 a0001c0001t0001g0311 a0001c0001t0002g0049 others(12): Show |
15 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.423+1285delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692596 | |||||||
chr18:692629 | AAAAAG | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.423+1248_423+1252d others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692629 | |||||||
chr18:692631 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.423+1251T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692631 | |||||||
chr18:692638 | A | G | 1 | a0003c0004t0003g0331 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.423+1244T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692638 | |||||||
chr18:692808 | C | T | 17 | a0001c0001t0001g0154 a0001c0001t0006g0048 a0001c0001t0006g0111 others(14): Show |
17 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+1074G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692808 | |||||||
chr18:692817 | A | T | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.423+1065T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692817 | |||||||
chr18:692889 | A | G | 2 | a0003c0007t0002g0338 a0003c0007t0002g0364 |
2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.423+993T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692889 | |||||||
chr18:692891 | C | A | 1 | a0005c0010t0002g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.423+991G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692891 | |||||||
chr18:692928 | CTT | C | 9 | a0001c0006t0004g0004 a0001c0006t0004g0012 a0001c0006t0004g0150 others(6): Show |
12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.423+952_423+953del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692928 | |||||||
chr18:692998 | C | T | 2 | a0001c0001t0002g0123 a0001c0001t0002g0167 |
2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.423+884G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692998 | |||||||
chr18:693073 | G | A | 1 | a0001c0003t0001g0247 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.423+809C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693073 | |||||||
chr18:693112 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.423+770C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693112 | |||||||
chr18:693266 | T | C | 1 | a0001c0001t0028g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.423+616A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693266 | |||||||
chr18:693269 | A | C | 81 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(78): Show |
84 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.423+613T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693269 | |||||||
chr18:693285 | A | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.423+597T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693285 | |||||||
chr18:693673 | C | T | 1 | a0002c0002t0005g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423+209G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693673 | |||||||
chr18:693674 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.423+208G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693674 | |||||||
chr18:693763 | T | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.423+119A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693763 | |||||||
chr18:693767 | C | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.423+115G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693767 | |||||||
chr18:693826 | T | A | 14 | a0002c0002t0006g0149 a0002c0002t0008g0062 a0002c0002t0008g0065 others(11): Show |
14 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+56A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693826 | |||||||
chr18:693828 | A | C | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.423+54T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693828 | |||||||
chr18:693931 | T | C | 1 | a0004c0008t0001g0367 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.397-23A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693931 | |||||||
chr18:693940 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.397-32T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693940 | |||||||
chr18:693943 | T | C | 1 | a0001c0001t0031g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.397-35A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693943 | |||||||
chr18:693977 | G | A | 187 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(184): Show |
200 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.397-69C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693977 | |||||||
chr18:693986 | GCT | G | 273 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(270): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.397-80_397-79delAG | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693986 | |||||||
chr18:694192 | A | G | 1 | a0001c0001t0010g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.396+56T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 694192 | |||||||
chr18:694206 | A | G | 277 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(274): Show |
293 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.396+42T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 694206 | |||||||
chr18:694538 | G | A | 42 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(39): Show |
43 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.310-204C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694538 | |||||||
chr18:694568 | C | T | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.310-234G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694568 | |||||||
chr18:694600 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.310-266G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694600 | |||||||
chr18:694627 | C | CA | 21 | a0001c0001t0001g0154 a0001c0001t0002g0036 a0001c0001t0002g0078 others(18): Show |
21 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.310-294dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694627 | |||||||
chr18:694635 | A | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.310-301T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694635 | |||||||
chr18:694653 | G | A | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.310-319C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694653 | |||||||
chr18:694678 | G | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.310-344C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694678 | |||||||
chr18:694703 | T | C | 86 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(83): Show |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-369A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694703 | |||||||
chr18:694784 | A | T | 1 | a0001c0006t0004g0304 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.310-450T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694784 | |||||||
chr18:694808 | T | TTCTC | 57 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(54): Show |
58 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.310-478_310-475dup others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694808 | |||||||
chr18:694818 | C | A | 16 | a0001c0001t0001g0154 a0001c0001t0006g0048 a0001c0001t0006g0155 others(13): Show |
16 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.310-484G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694818 | |||||||
chr18:694818 | C | CTCTA | 25 | a0002c0002t0002g0303 a0002c0002t0004g0008 a0002c0002t0004g0032 others(22): Show |
27 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.310-485_310-484ins others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694818 | |||||||
chr18:694868 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.310-534A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694868 | |||||||
chr18:694902 | G | C | 1 | a0003c0007t0003g0345 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.310-568C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694902 | |||||||
chr18:695030 | G | A | 58 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(55): Show |
59 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.310-696C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695030 | |||||||
chr18:695105 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.310-771G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695105 | |||||||
chr18:695136 | C | A | 1 | a0001c0001t0002g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.310-802G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695136 | |||||||
chr18:695252 | T | G | 4 | a0001c0003t0001g0247 a0001c0003t0001g0251 a0001c0003t0001g0300 others(1): Show |
4 | HG02015.hp1 NA18955.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-918A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695252 | |||||||
chr18:695297 | G | A | 3 | a0001c0003t0001g0276 a0001c0003t0001g0316 a0001c0017t0001g0328 |
3 | NA18981.hp1 NA19005.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.310-963C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695297 | |||||||
chr18:695319 | T | C | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.310-985A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695319 | |||||||
chr18:695322 | T | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.310-988A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695322 | |||||||
chr18:695367 | G | A | 58 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(55): Show |
59 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.310-1033C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695367 | |||||||
chr18:695467 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.310-1133G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695467 | |||||||
chr18:695558 | A | ATGG | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.310-1227_310-1225d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695558 | |||||||
chr18:695738 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.310-1404G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695738 | |||||||
chr18:695959 | T | C | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+1281A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695959 | |||||||
chr18:695980 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.309+1260G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695980 | |||||||
chr18:695981 | G | A | 1 | a0003c0007t0002g0337 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.309+1259C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695981 | |||||||
chr18:696082 | T | C | 1 | a0003c0004t0002g0342 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.309+1158A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696082 | |||||||
chr18:696204 | C | CT | 12 | a0001c0001t0001g0056 a0001c0001t0001g0263 a0001c0001t0001g0268 others(9): Show |
12 | HG01358.hp1 HG01516.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.309+1035dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | |||||||
chr18:696204 | C | CTT | 157 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0006 others(154): Show |
170 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.309+1034_309+1035d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | |||||||
chr18:696204 | C | CTTT | 12 | a0001c0001t0001g0154 a0001c0001t0002g0036 a0001c0001t0002g0086 others(9): Show |
12 | HG00673.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+1033_309+1035d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | |||||||
chr18:696204 | CTT | C | 81 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(78): Show |
84 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.309+1034_309+1035d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | |||||||
chr18:696204 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0002g0035 a0001c0001t0002g0040 a0001c0001t0002g0055 others(3): Show |
6 | NA18941.hp1 NA18984.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1026_309+1035d others(12): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | |||||||
chr18:696254 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.309+986G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696254 | |||||||
chr18:696274 | C | T | 1 | a0001c0001t0031g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.309+966G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696274 | |||||||
chr18:696302 | C | G | 1 | a0001c0001t0002g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.309+938G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696302 | |||||||
chr18:696313 | G | A | 1 | a0002c0002t0027g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.309+927C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696313 | |||||||
chr18:696360 | C | T | 1 | a0002c0002t0005g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.309+880G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696360 | |||||||
chr18:696401 | C | T | 1 | a0005c0010t0025g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+839G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696401 | |||||||
chr18:696451 | T | C | 1 | a0001c0001t0011g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.309+789A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696451 | |||||||
chr18:696478 | T | C | 4 | a0003c0004t0001g0383 a0003c0004t0003g0334 a0003c0004t0003g0361 others(1): Show |
4 | HG00544.hp2 NA18747.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+762A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696478 | |||||||
chr18:696501 | G | A | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+739C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696501 | |||||||
chr18:696502 | C | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+738G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696502 | |||||||
chr18:696533 | C | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+707G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696533 | |||||||
chr18:696583 | C | A | 8 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+657G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696583 | |||||||
chr18:696645 | T | C | 85 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(82): Show |
88 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.309+595A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696645 | |||||||
chr18:696667 | C | T | 3 | a0004c0008t0001g0352 a0004c0008t0001g0353 a0004c0008t0001g0367 |
3 | HG01257.hp2 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.309+573G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696667 | |||||||
chr18:696703 | A | G | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+537T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696703 | |||||||
chr18:696748 | T | C | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+492A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696748 | |||||||
chr18:696842 | C | A | 2 | a0002c0002t0005g0279 a0002c0002t0005g0280 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.309+398G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696842 | |||||||
chr18:696892 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.309+348C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696892 | |||||||
chr18:696915 | G | A | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.309+325C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696915 | |||||||
chr18:696933 | G | A | 1 | a0002c0002t0004g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.309+307C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696933 | |||||||
chr18:697049 | G | A | 3 | a0001c0001t0002g0128 a0001c0001t0002g0130 a0001c0001t0002g0172 |
3 | HG03490.hp2 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.309+191C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697049 | |||||||
chr18:697065 | C | T | 17 | a0001c0001t0001g0154 a0001c0001t0006g0048 a0001c0001t0006g0111 others(14): Show |
17 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.309+175G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697065 | |||||||
chr18:697066 | A | G | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+174T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697066 | |||||||
chr18:697123 | TAAATAAA others(5): Show |
T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0229 |
2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.309+105_309+116del others(12): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697123 | |||||||
chr18:697147 | C | T | 1 | a0001c0003t0001g0282 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.309+93G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697147 | |||||||
chr18:697377 | CTT | C | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-24_194-23delAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697377 | |||||||
chr18:697622 | G | A | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.194-267C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697622 | |||||||
chr18:697699 | C | T | 1 | a0001c0003t0001g0274 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.194-344G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697699 | |||||||
chr18:697857 | T | C | 174 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0001g0059 others(171): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.194-502A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697857 | |||||||
chr18:697912 | G | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-557C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697912 | |||||||
chr18:697922 | A | G | 86 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(83): Show |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.194-567T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697922 | |||||||
chr18:697927 | A | G | 86 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(83): Show |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.194-572T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697927 | |||||||
chr18:697938 | C | A | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-583G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697938 | |||||||
chr18:697943 | G | A | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-588C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697943 | |||||||
chr18:697945 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.194-590G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697945 | |||||||
chr18:698024 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(103): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.194-669C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698024 | |||||||
chr18:698225 | T | C | 1 | a0001c0001t0033g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194-870A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698225 | |||||||
chr18:698227 | G | A | 1 | a0001c0003t0001g0277 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.194-872C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698227 | |||||||
chr18:698311 | C | T | 21 | a0002c0002t0001g0104 a0002c0002t0002g0232 a0002c0002t0005g0178 others(18): Show |
22 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.194-956G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698311 | |||||||
chr18:698312 | A | G | 86 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(83): Show |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.194-957T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698312 | |||||||
chr18:698491 | T | C | 7 | a0002c0002t0008g0062 a0002c0002t0008g0065 a0002c0002t0008g0107 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-1136A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698491 | |||||||
chr18:698589 | G | A | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-1234C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698589 | |||||||
chr18:698624 | A | AATTATT | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-1275_194-1270d others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698624 | |||||||
chr18:698696 | T | C | 2 | a0001c0001t0014g0079 a0001c0001t0014g0205 |
2 | NA18995.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.194-1341A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698696 | |||||||
chr18:698738 | C | T | 1 | a0005c0010t0025g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.194-1383G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698738 | |||||||
chr18:699120 | G | T | 82 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-1765C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699120 | |||||||
chr18:699281 | G | A | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-1926C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699281 | |||||||
chr18:699478 | A | AAAT | 9 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0001t0001g0252 others(6): Show |
9 | HG00642.hp1 HG01074.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-2126_194-2124d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | |||||||
chr18:699478 | A | AAATAATA others(11): Show |
2 | a0002c0002t0009g0034 a0002c0015t0002g0257 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.194-2141_194-2124d others(20): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | |||||||
chr18:699478 | A | AAATAATA others(14): Show |
1 | a0008c0014t0022g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.194-2144_194-2124d others(23): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | |||||||
chr18:699478 | AAAT | A | 82 | a0002c0002t0001g0104 a0002c0002t0002g0103 a0002c0002t0002g0192 others(79): Show |
85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-2126_194-2124d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | |||||||
chr18:699478 | AAATAAT | A | 186 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(183): Show |
199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.194-2129_194-2124d others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | |||||||
chr18:699530 | A | T | 1 | a0001c0003t0001g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.194-2175T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699530 | |||||||
chr18:699755 | G | A | 1 | a0002c0002t0004g0060 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.194-2400C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699755 | |||||||
chr18:699805 | C | A | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-2450G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699805 | |||||||
chr18:699881 | A | G | 83 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-2526T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699881 | |||||||
chr18:700039 | C | A | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.194-2684G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700039 | |||||||
chr18:700041 | T | C | 1 | a0001c0003t0001g0325 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.194-2686A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700041 | |||||||
chr18:700086 | A | G | 2 | a0002c0002t0009g0098 a0002c0002t0009g0134 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194-2731T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700086 | |||||||
chr18:700612 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.194-3257G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700612 | |||||||
chr18:700687 | T | C | 272 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(269): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.194-3332A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700687 | |||||||
chr18:700878 | G | A | 57 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(54): Show |
58 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.194-3523C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700878 | |||||||
chr18:700890 | C | CA | 64 | a0001c0001t0001g0017 a0001c0001t0001g0190 a0001c0001t0001g0220 others(61): Show |
66 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.194-3536dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | |||||||
chr18:700890 | C | CAA | 28 | a0001c0001t0006g0048 a0001c0001t0006g0155 a0001c0001t0006g0156 others(25): Show |
28 | HG00642.hp2 HG00673.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-3537_194-3536d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | |||||||
chr18:700890 | CA | C | 104 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0006 others(101): Show |
115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.194-3536delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | |||||||
chr18:700890 | CAA | C | 16 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(13): Show |
17 | HG00438.hp2 HG01261.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-3537_194-3536d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | |||||||
chr18:700890 | CAAA | C | 34 | a0001c0001t0031g0319 a0003c0004t0002g0342 a0003c0004t0002g0376 others(31): Show |
36 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.194-3538_194-3536d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | |||||||
chr18:700916 | A | G | 273 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(270): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.194-3561T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700916 | |||||||
chr18:700951 | G | T | 2 | a0001c0001t0017g0193 a0001c0001t0017g0237 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.194-3596C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700951 | |||||||
chr18:701022 | A | G | 1 | a0003c0004t0004g0340 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.194-3667T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701022 | |||||||
chr18:701192 | A | G | 6 | a0001c0001t0007g0014 a0001c0001t0007g0016 a0001c0001t0007g0218 others(3): Show |
8 | NA18948.hp1 NA18969.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-3837T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701192 | |||||||
chr18:701193 | T | G | 1 | a0001c0001t0007g0243 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.194-3838A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701193 | |||||||
chr18:701219 | A | G | 1 | a0003c0004t0002g0376 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.194-3864T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701219 | |||||||
chr18:701464 | A | AC | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-4110_194-4109i others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701464 | |||||||
chr18:701572 | T | C | 271 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(268): Show |
287 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.194-4217A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701572 | |||||||
chr18:701598 | T | A | 1 | a0001c0001t0002g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.194-4243A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701598 | |||||||
chr18:701749 | T | C | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-4394A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701749 | |||||||
chr18:701752 | A | G | 94 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(91): Show |
97 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.194-4397T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701752 | |||||||
chr18:701756 | C | CAA | 84 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0235 others(81): Show |
87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-4403_194-4402d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701756 | |||||||
chr18:701756 | CA | C | 187 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(184): Show |
200 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.194-4402delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701756 | |||||||
chr18:701780 | C | T | 1 | a0001c0006t0004g0236 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.194-4425G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701780 | |||||||
chr18:701939 | G | GATAA | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+4527_193+4530d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701939 | |||||||
chr18:701939 | G | GATAAATA others(1): Show |
34 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0235 others(31): Show |
36 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.193+4523_193+4530d others(10): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701939 | |||||||
chr18:701939 | G | GATAAATA others(5): Show |
10 | a0002c0002t0006g0149 a0002c0002t0008g0062 a0002c0002t0008g0065 others(7): Show |
10 | HG01192.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+4519_193+4530d others(14): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701939 | |||||||
chr18:702014 | G | A | 274 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(271): Show |
290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.193+4456C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702014 | |||||||
chr18:702077 | A | G | 43 | a0001c0013t0002g0148 a0003c0004t0001g0383 a0003c0004t0002g0342 others(40): Show |
45 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.193+4393T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702077 | |||||||
chr18:702098 | T | C | 86 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0235 others(83): Show |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.193+4372A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702098 | |||||||
chr18:702196 | T | G | 271 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(268): Show |
287 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.193+4274A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702196 | |||||||
chr18:702217 | T | C | 86 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0235 others(83): Show |
89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.193+4253A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702217 | |||||||
chr18:702264 | C | CA | 71 | a0001c0001t0001g0242 a0001c0003t0001g0140 a0001c0003t0001g0235 others(68): Show |
73 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.193+4205dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | |||||||
chr18:702264 | C | CAA | 16 | a0001c0003t0001g0139 a0002c0002t0002g0192 a0002c0002t0004g0032 others(13): Show |
17 | HG01074.hp2 HG01123.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+4204_193+4205d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | |||||||
chr18:702264 | CA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(148): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.193+4205delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | |||||||
chr18:702264 | CAA | C | 114 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(111): Show |
122 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.193+4204_193+4205d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | |||||||
chr18:702439 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.193+4031C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702439 | |||||||
chr18:702512 | C | T | 271 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(268): Show |
287 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.193+3958G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702512 | |||||||
chr18:702617 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(84): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.193+3853C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702617 | |||||||
chr18:702632 | C | T | 5 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+3838G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702632 | |||||||
chr18:702656 | T | C | 1 | a0002c0002t0027g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.193+3814A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702656 | |||||||
chr18:702862 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.193+3608T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702862 | |||||||
chr18:702993 | G | C | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.193+3477C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702993 | |||||||
chr18:703032 | T | A | 1 | a0002c0002t0012g0131 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+3438A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703032 | |||||||
chr18:703062 | T | C | 1 | a0001c0001t0011g0194 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.193+3408A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703062 | |||||||
chr18:703087 | G | A | 9 | a0003c0004t0003g0021 a0003c0004t0003g0332 a0003c0004t0003g0336 others(6): Show |
10 | HG00438.hp2 HG00621.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+3383C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703087 | |||||||
chr18:703185 | G | A | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+3285C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703185 | |||||||
chr18:703216 | G | A | 2 | a0001c0003t0001g0276 a0001c0003t0001g0316 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.193+3254C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703216 | |||||||
chr18:703302 | T | C | 1 | a0001c0003t0001g0277 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.193+3168A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703302 | |||||||
chr18:703388 | AT | A | 272 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(269): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.193+3081delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703388 | |||||||
chr18:703442 | G | A | 272 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0154 others(269): Show |
288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.193+3028C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703442 | |||||||
chr18:703446 | G | T | 1 | a0002c0002t0002g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.193+3024C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703446 | |||||||
chr18:703472 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193+2998T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703472 | |||||||
chr18:703544 | T | A | 1 | a0001c0003t0001g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.193+2926A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703544 | |||||||
chr18:703785 | G | C | 277 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(274): Show |
293 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.193+2685C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703785 | |||||||
chr18:703853 | T | G | 1 | a0001c0003t0001g0297 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.193+2617A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703853 | |||||||
chr18:704120 | C | T | 3 | a0002c0002t0009g0093 a0002c0002t0009g0094 a0002c0002t0027g0321 |
3 | HG02258.hp1 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.193+2350G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704120 | |||||||
chr18:704191 | TGAGAGGC others(12): Show |
T | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.193+2260_193+2278d others(21): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704191 | |||||||
chr18:704232 | G | A | 267 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(264): Show |
283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+2238C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704232 | |||||||
chr18:704246 | T | C | 198 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(195): Show |
211 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.193+2224A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704246 | |||||||
chr18:704262 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.193+2208A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704262 | |||||||
chr18:704381 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.193+2089A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704381 | |||||||
chr18:704407 | A | G | 267 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(264): Show |
283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+2063T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704407 | |||||||
chr18:704440 | G | GA | 8 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+2029dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | |||||||
chr18:704440 | G | GAAA | 6 | a0002c0002t0012g0026 a0002c0002t0012g0091 a0002c0002t0012g0131 others(3): Show |
6 | HG01192.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+2027_193+2029d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | |||||||
chr18:704440 | G | GAAAA | 87 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0001t0002g0061 others(84): Show |
92 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.193+2026_193+2029d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | |||||||
chr18:704440 | G | GAAAAA | 105 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(102): Show |
113 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.193+2025_193+2029d others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | |||||||
chr18:704440 | G | GAAAAAA | 52 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0072 others(49): Show |
55 | HG00423.hp1 HG01074.hp2 HG01257.hp2 others(52): Show |
intron_variant | MODIFIER | c.193+2024_193+2029d others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | |||||||
chr18:704440 | G | GAAAAAAA | 14 | a0001c0001t0001g0154 a0001c0001t0002g0087 a0001c0001t0006g0226 others(11): Show |
14 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.193+2023_193+2029d others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | |||||||
chr18:704444 | A | G | 2 | a0001c0001t0017g0193 a0001c0001t0017g0237 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.193+2026T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704444 | |||||||
chr18:704535 | T | C | 1 | a0001c0001t0031g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193+1935A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704535 | |||||||
chr18:704569 | G | T | 24 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0003t0001g0139 others(21): Show |
25 | HG00408.hp2 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.193+1901C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704569 | |||||||
chr18:704578 | T | C | 1 | a0002c0002t0018g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.193+1892A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704578 | |||||||
chr18:704605 | C | CT | 168 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0002g0002 others(165): Show |
180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.193+1864dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704605 | |||||||
chr18:704605 | C | CTT | 29 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0001t0002g0037 others(26): Show |
30 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.193+1863_193+1864d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704605 | |||||||
chr18:704605 | C | CTTT | 8 | a0001c0001t0002g0072 a0001c0001t0002g0117 a0001c0003t0001g0139 others(5): Show |
8 | HG00408.hp2 HG02155.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1862_193+1864d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704605 | |||||||
chr18:704611 | TC | T | 10 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(7): Show |
10 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+1858delG | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704611 | |||||||
chr18:704612 | C | T | 256 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(253): Show |
272 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.193+1858G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704612 | |||||||
chr18:704667 | G | A | 1 | a0006c0009t0001g0191 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.193+1803C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704667 | |||||||
chr18:704699 | A | C | 1 | a0002c0002t0005g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193+1771T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704699 | |||||||
chr18:704804 | C | G | 203 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(200): Show |
216 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.193+1666G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704804 | |||||||
chr18:704825 | T | C | 203 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(200): Show |
216 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.193+1645A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704825 | |||||||
chr18:704826 | G | A | 20 | a0002c0002t0001g0104 a0002c0002t0002g0232 a0002c0002t0005g0178 others(17): Show |
21 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.193+1644C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704826 | |||||||
chr18:704853 | G | A | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.193+1617C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704853 | |||||||
chr18:704901 | T | C | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.193+1569A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704901 | |||||||
chr18:704935 | G | A | 1 | a0002c0002t0008g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+1535C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704935 | |||||||
chr18:704955 | C | CAGG | 273 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(270): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.193+1514_193+1515i others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704955 | |||||||
chr18:705087 | C | T | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.193+1383G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705087 | |||||||
chr18:705147 | G | A | 1 | a0004c0008t0004g0019 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.193+1323C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705147 | |||||||
chr18:705173 | G | A | 1 | a0002c0005t0001g0027 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.193+1297C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705173 | |||||||
chr18:705257 | C | A | 1 | a0002c0002t0008g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+1213G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705257 | |||||||
chr18:705361 | AT | A | 7 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+1108delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705361 | |||||||
chr18:705489 | C | T | 8 | a0001c0001t0033g0109 a0002c0002t0008g0062 a0002c0002t0008g0107 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+981G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705489 | |||||||
chr18:705519 | C | T | 24 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0003t0001g0139 others(21): Show |
25 | HG00408.hp2 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.193+951G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705519 | |||||||
chr18:705537 | T | C | 1 | a0003c0004t0003g0357 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193+933A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705537 | |||||||
chr18:705550 | CTGTT | C | 7 | a0002c0002t0008g0062 a0002c0002t0008g0107 a0002c0002t0008g0108 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+916_193+919del others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705550 | |||||||
chr18:705598 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(325): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.193+872A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705598 | |||||||
chr18:705648 | G | A | 1 | a0002c0002t0008g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+822C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705648 | |||||||
chr18:705658 | G | A | 56 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(53): Show |
59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.193+812C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705658 | |||||||
chr18:705686 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.193+784A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705686 | |||||||
chr18:705695 | G | T | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.193+775C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705695 | |||||||
chr18:705753 | A | G | 5 | a0001c0001t0001g0189 a0001c0001t0001g0216 a0001c0001t0001g0261 others(2): Show |
5 | HG00558.hp2 HG00597.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+717T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705753 | |||||||
chr18:705755 | T | C | 7 | a0002c0002t0008g0062 a0002c0002t0008g0107 a0002c0002t0008g0108 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+715A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705755 | |||||||
chr18:705788 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193+682G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705788 | |||||||
chr18:705820 | T | C | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.193+650A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705820 | |||||||
chr18:705996 | G | C | 1 | a0001c0001t0002g0058 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.193+474C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705996 | |||||||
chr18:706047 | G | T | 273 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(270): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.193+423C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706047 | |||||||
chr18:706092 | G | A | 46 | a0001c0013t0002g0148 a0003c0004t0001g0383 a0003c0004t0002g0342 others(43): Show |
49 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.193+378C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706092 | |||||||
chr18:706125 | C | T | 1 | a0001c0001t0002g0023 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.193+345G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706125 | |||||||
chr18:706182 | T | C | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.193+288A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706182 | |||||||
chr18:706183 | C | T | 202 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(199): Show |
215 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.193+287G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706183 | |||||||
chr18:706187 | G | T | 1 | a0001c0001t0010g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.193+283C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706187 | |||||||
chr18:706206 | G | A | 56 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(53): Show |
59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.193+264C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706206 | |||||||
chr18:706322 | C | CACTG | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.193+147_193+148ins others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706322 | |||||||
chr18:706348 | A | T | 2 | a0002c0002t0009g0034 a0008c0014t0022g0158 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.193+122T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706348 | |||||||
chr18:706450 | C | T | 1 | a0002c0002t0008g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+20G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706450 | |||||||
chr18:706589 | A | G | 273 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(270): Show |
289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.85-11T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706589 | |||||||
chr18:706626 | C | T | 1 | a0003c0004t0003g0365 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.85-48G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706626 | |||||||
chr18:706801 | G | GTATA | 3 | a0002c0002t0009g0034 a0002c0015t0002g0257 a0008c0014t0022g0158 |
3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.85-227_85-224dupTA others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | |||||||
chr18:706801 | G | GTATATAT others(1): Show |
12 | a0001c0001t0001g0088 a0001c0001t0002g0010 a0001c0001t0002g0025 others(9): Show |
13 | HG00741.hp1 HG01106.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.85-231_85-224dupTA others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | |||||||
chr18:706801 | G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0127 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.85-233_85-224dupTA others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | |||||||
chr18:706801 | G | GTGTATA | 7 | a0003c0004t0003g0341 a0003c0004t0003g0350 a0003c0004t0003g0351 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-224_85-223insTA others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | |||||||
chr18:706801 | G | GTGTATAT others(1): Show |
16 | a0003c0004t0003g0021 a0003c0004t0003g0331 a0003c0004t0003g0332 others(13): Show |
17 | HG00423.hp1 HG02004.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.85-224_85-223insTA others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | |||||||
chr18:706803 | A | G | 38 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(35): Show |
40 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.85-225T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706803 | |||||||
chr18:706810 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-232A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706810 | |||||||
chr18:706812 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-234A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706812 | |||||||
chr18:706813 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-235T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706813 | |||||||
chr18:706813 | A | T | 1 | a0003c0007t0010g0381 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.85-235T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706813 | |||||||
chr18:706814 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-236A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706814 | |||||||
chr18:706815 | A | ATATAT | 8 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-238_85-237insAT others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATATAT | 78 | a0001c0001t0001g0180 a0001c0001t0002g0002 a0001c0001t0002g0006 others(75): Show |
84 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.85-238_85-237insAT others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATATAT others(2): Show |
7 | a0001c0001t0001g0056 a0001c0001t0002g0007 a0001c0001t0002g0058 others(4): Show |
7 | HG01516.hp2 HG02300.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-238_85-237insAT others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATATAT others(4): Show |
1 | a0001c0006t0004g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-238_85-237insAT others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATATAT others(4): Show |
1 | a0002c0002t0006g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.85-238_85-237insAA others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATATAT others(1): Show |
22 | a0001c0001t0002g0007 a0001c0001t0002g0028 a0001c0001t0002g0029 others(19): Show |
22 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.85-238_85-237insAA others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATATTT | 10 | a0001c0001t0002g0170 a0001c0001t0002g0199 a0001c0013t0002g0148 others(7): Show |
11 | HG01074.hp2 HG01261.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.85-238_85-237insAA others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | ATATTT | 6 | a0002c0002t0008g0062 a0002c0002t0008g0107 a0002c0002t0008g0108 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-238_85-237insAA others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-237T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | A | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0189 a0001c0001t0001g0216 others(43): Show |
49 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.85-237T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706815 | AT | A | 8 | a0001c0001t0001g0242 a0001c0001t0017g0193 a0001c0001t0017g0237 others(5): Show |
9 | HG00673.hp2 HG01361.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-238delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | |||||||
chr18:706816 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-238A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706816 | T | TA | 6 | a0001c0001t0001g0223 a0001c0001t0001g0252 a0001c0001t0001g0281 others(3): Show |
6 | HG00639.hp2 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-239_85-238insT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706816 | T | TATATA | 7 | a0002c0002t0005g0187 a0002c0002t0012g0026 a0002c0002t0012g0091 others(4): Show |
7 | HG02809.hp1 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706816 | T | TATATATA | 68 | a0001c0001t0001g0059 a0001c0001t0002g0043 a0001c0001t0002g0128 others(65): Show |
70 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706816 | T | TATATATA others(2): Show |
3 | a0001c0001t0033g0109 a0002c0002t0008g0065 a0003c0004t0003g0358 |
3 | HG02523.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.85-239_85-238insTA others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706816 | T | TATATATA others(4): Show |
4 | a0001c0006t0004g0004 a0001c0006t0004g0150 a0001c0006t0004g0236 others(1): Show |
6 | HG01496.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706816 | T | TATATATA others(6): Show |
5 | a0001c0006t0004g0012 a0001c0006t0004g0151 a0001c0006t0004g0238 others(2): Show |
6 | HG01884.hp2 HG02109.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(11): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | |||||||
chr18:706817 | T | A | 16 | a0001c0001t0001g0326 a0001c0001t0002g0090 a0001c0001t0002g0164 others(13): Show |
16 | HG00741.hp1 HG01106.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.85-239A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706817 | |||||||
chr18:706817 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-239A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706817 | |||||||
chr18:706818 | T | A | 47 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(44): Show |
49 | HG00280.hp1 HG00408.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.85-240A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706818 | |||||||
chr18:706818 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-240A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706818 | |||||||
chr18:706819 | T | A | 9 | a0001c0001t0001g0327 a0001c0001t0006g0048 a0001c0001t0006g0111 others(6): Show |
9 | HG01106.hp1 HG01934.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-241A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706819 | |||||||
chr18:706820 | T | A | 30 | a0002c0002t0001g0104 a0002c0002t0002g0103 a0002c0002t0002g0232 others(27): Show |
31 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.85-242A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706820 | |||||||
chr18:706820 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-242A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706820 | |||||||
chr18:706821 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-243A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706821 | |||||||
chr18:706822 | T | A | 2 | a0001c0001t0001g0327 a0002c0005t0001g0068 |
2 | HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.85-244A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706822 | |||||||
chr18:706824 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-246A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706824 | |||||||
chr18:706944 | G | A | 1 | a0001c0003t0001g0013 | 2 | NA18999.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.85-366C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706944 | |||||||
chr18:706957 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-379A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706957 | |||||||
chr18:706961 | G | C | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-383C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706961 | |||||||
chr18:706962 | G | T | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-384C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706962 | |||||||
chr18:706964 | A | T | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-386T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706964 | |||||||
chr18:706965 | C | T | 210 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(207): Show |
223 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.85-387G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706965 | |||||||
chr18:706966 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-388C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706966 | |||||||
chr18:706967 | T | G | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-389A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706967 | |||||||
chr18:706968 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-390C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706968 | |||||||
chr18:706969 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-391G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706969 | |||||||
chr18:706970 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-392G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706970 | |||||||
chr18:707431 | A | C | 3 | a0001c0003t0001g0240 a0001c0003t0001g0260 a0001c0003t0001g0289 |
3 | HG00673.hp2 NA18961.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.85-853T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707431 | |||||||
chr18:707470 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.85-892C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707470 | |||||||
chr18:707497 | T | C | 266 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(263): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.85-919A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707497 | |||||||
chr18:707511 | G | C | 40 | a0002c0002t0001g0096 a0002c0002t0001g0104 a0002c0002t0002g0103 others(37): Show |
41 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.85-933C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707511 | |||||||
chr18:707560 | A | C | 267 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(264): Show |
283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.85-982T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707560 | |||||||
chr18:707592 | T | C | 1 | a0003c0004t0003g0359 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.85-1014A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707592 | |||||||
chr18:707637 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0005g0288 |
2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.85-1059T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707637 | |||||||
chr18:707732 | GTTTAA | G | 56 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(53): Show |
59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.85-1159_85-1155del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707732 | |||||||
chr18:707851 | TTTA | T | 276 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(273): Show |
292 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.85-1276_85-1274del others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707851 | |||||||
chr18:708023 | C | CT | 52 | a0001c0001t0001g0305 a0001c0001t0002g0198 a0001c0003t0001g0215 others(49): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.85-1446dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708023 | |||||||
chr18:708023 | CT | C | 189 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(186): Show |
202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.85-1446delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708023 | |||||||
chr18:708063 | G | T | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1485C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708063 | |||||||
chr18:708066 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1488C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708066 | |||||||
chr18:708068 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1490G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708068 | |||||||
chr18:708069 | C | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1491G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708069 | |||||||
chr18:708071 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1493C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708071 | |||||||
chr18:708074 | T | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1496A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708074 | |||||||
chr18:708075 | G | T | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1497C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708075 | |||||||
chr18:708077 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1499A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708077 | |||||||
chr18:708078 | C | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1500G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708078 | |||||||
chr18:708081 | G | T | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1503C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708081 | |||||||
chr18:708082 | A | T | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1504T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708082 | |||||||
chr18:708083 | A | C | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1505T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708083 | |||||||
chr18:708085 | T | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1507A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708085 | |||||||
chr18:708089 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1511C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708089 | |||||||
chr18:708093 | T | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1515A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708093 | |||||||
chr18:708114 | G | C | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1536C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708114 | |||||||
chr18:708136 | C | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1558G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708136 | |||||||
chr18:708137 | A | C | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1559T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708137 | |||||||
chr18:708138 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1560C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708138 | |||||||
chr18:708150 | C | CACGCCCA others(3): Show |
1 | a0001c0001t0002g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1573_85-1572ins others(10): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708150 | |||||||
chr18:708157 | G | A | 7 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-1579C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708157 | |||||||
chr18:708207 | C | T | 6 | a0002c0002t0005g0178 a0002c0002t0005g0179 a0002c0005t0001g0067 others(3): Show |
6 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-1629G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708207 | |||||||
chr18:708237 | G | C | 1 | a0001c0001t0001g0318 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.85-1659C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708237 | |||||||
chr18:708299 | T | C | 267 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(264): Show |
283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.85-1721A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708299 | |||||||
chr18:708586 | C | T | 1 | a0002c0002t0008g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85-2008G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708586 | |||||||
chr18:708710 | C | G | 268 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(265): Show |
284 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.85-2132G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708710 | |||||||
chr18:709140 | C | A | 1 | a0004c0008t0004g0382 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.85-2562G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709140 | |||||||
chr18:709179 | G | A | 8 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-2601C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709179 | |||||||
chr18:709202 | G | A | 61 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(58): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.85-2624C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709202 | |||||||
chr18:709232 | C | T | 204 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(201): Show |
217 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.85-2654G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709232 | |||||||
chr18:709293 | G | C | 24 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0003t0001g0139 others(21): Show |
25 | HG00408.hp2 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.85-2715C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709293 | |||||||
chr18:709379 | A | G | 267 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(264): Show |
283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.85-2801T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709379 | |||||||
chr18:709396 | G | A | 3 | a0002c0002t0020g0105 a0002c0005t0001g0146 a0002c0005t0001g0186 |
3 | HG01123.hp2 HG01192.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.85-2818C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709396 | |||||||
chr18:709590 | G | T | 267 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(264): Show |
283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.84+2914C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709590 | |||||||
chr18:709679 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.84+2825C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709679 | |||||||
chr18:709834 | T | A | 1 | a0003c0004t0003g0360 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.84+2670A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709834 | |||||||
chr18:709950 | C | T | 6 | a0002c0002t0008g0062 a0002c0002t0008g0107 a0002c0002t0008g0108 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2554G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709950 | |||||||
chr18:710143 | C | T | 1 | a0003c0004t0003g0339 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.84+2361G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710143 | |||||||
chr18:710146 | T | A | 60 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(57): Show |
63 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.84+2358A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710146 | |||||||
chr18:710177 | C | G | 1 | a0001c0001t0002g0197 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.84+2327G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710177 | |||||||
chr18:710265 | C | T | 59 | a0001c0001t0001g0154 a0001c0001t0006g0226 a0001c0001t0011g0046 others(56): Show |
62 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.84+2239G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710265 | |||||||
chr18:710388 | G | C | 4 | a0003c0004t0001g0383 a0003c0004t0003g0334 a0003c0004t0003g0361 others(1): Show |
4 | HG00544.hp2 NA18747.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+2116C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710388 | |||||||
chr18:710534 | G | T | 1 | a0002c0002t0005g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.84+1970C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710534 | |||||||
chr18:710554 | G | A | 7 | a0001c0001t0006g0048 a0001c0001t0006g0111 a0001c0001t0006g0155 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+1950C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710554 | |||||||
chr18:710560 | G | A | 1 | a0003c0004t0003g0384 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.84+1944C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710560 | |||||||
chr18:710854 | G | C | 1 | a0002c0002t0005g0213 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.84+1650C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710854 | |||||||
chr18:710883 | T | C | 1 | a0002c0002t0020g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.84+1621A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710883 | |||||||
chr18:710980 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.84+1524C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710980 | |||||||
chr18:711017 | G | A | 68 | a0001c0001t0001g0154 a0001c0001t0006g0048 a0001c0001t0006g0111 others(65): Show |
71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.84+1487C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711017 | |||||||
chr18:711066 | A | T | 3 | a0001c0001t0002g0066 a0001c0001t0002g0195 a0001c0001t0002g0196 |
3 | HG03491.hp1 HG03492.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.84+1438T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711066 | |||||||
chr18:711167 | C | T | 8 | a0001c0001t0033g0109 a0002c0002t0008g0062 a0002c0002t0008g0107 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+1337G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711167 | |||||||
chr18:711334 | T | C | 1 | a0001c0003t0001g0284 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84+1170A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711334 | |||||||
chr18:711341 | G | A | 69 | a0001c0001t0001g0154 a0001c0001t0006g0048 a0001c0001t0006g0111 others(66): Show |
72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.84+1163C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711341 | |||||||
chr18:711370 | G | A | 1 | a0002c0002t0008g0065 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.84+1134C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711370 | |||||||
chr18:711462 | T | C | 14 | a0001c0006t0004g0004 a0001c0006t0004g0012 a0001c0006t0004g0150 others(11): Show |
17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.84+1042A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711462 | |||||||
chr18:711559 | G | C | 189 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(186): Show |
202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.84+945C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711559 | |||||||
chr18:711845 | G | C | 1 | a0001c0001t0013g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.84+659C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711845 | |||||||
chr18:711919 | C | T | 1 | a0001c0003t0001g0013 | 2 | NA18999.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.84+585G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711919 | |||||||
chr18:712037 | G | A | 190 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(187): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.84+467C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712037 | |||||||
chr18:712263 | T | G | 6 | a0001c0001t0001g0255 a0001c0001t0010g0224 a0001c0001t0010g0225 others(3): Show |
6 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+241A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712263 | |||||||
chr18:712319 | TCGG | T | 270 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(267): Show |
286 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.84+182_84+184delCC others(1): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712319 | |||||||
chr18:712331 | G | C | 1 | a0001c0001t0002g0188 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.84+173C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712331 | |||||||
chr18:712349 | G | GCCGCGCG others(11): Show |
1 | a0001c0003t0001g0256 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.84+137_84+154dupAC others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(11): Show |
11 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(8): Show |
11 | HG00609.hp2 HG01891.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(29): Show |
22 | a0001c0001t0001g0212 a0001c0001t0002g0195 a0001c0001t0002g0196 others(19): Show |
22 | HG00408.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(47): Show |
47 | a0001c0001t0001g0154 a0001c0001t0001g0180 a0001c0001t0002g0002 others(44): Show |
52 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(52): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(65): Show |
63 | a0001c0001t0001g0147 a0001c0001t0002g0009 a0001c0001t0002g0010 others(60): Show |
67 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(70): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(83): Show |
63 | a0001c0001t0001g0088 a0001c0001t0002g0066 a0001c0001t0002g0069 others(60): Show |
67 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(88): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(101): Show |
26 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0002g0007 others(23): Show |
27 | HG00558.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(106): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(119): Show |
15 | a0001c0001t0002g0006 a0001c0001t0002g0035 a0001c0001t0002g0036 others(12): Show |
16 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(124): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(137): Show |
9 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0031 others(6): Show |
9 | HG00408.hp1 HG00544.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(142): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | G | GCCGCGCT others(155): Show |
5 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0002c0002t0012g0026 others(2): Show |
5 | HG01943.hp2 HG02135.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(160): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | GCCGCGCG others(11): Show |
G | 1 | a0001c0001t0002g0285 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.84+137_84+154delAC others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712349 | GCCGCGCG others(29): Show |
G | 1 | a0002c0002t0002g0303 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.84+119_84+154delAC others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | |||||||
chr18:712356 | G | GTACCATG others(11): Show |
25 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(22): Show |
28 | HG00673.hp2 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.84+130_84+147dupAG others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | G | GTACCATG others(29): Show |
12 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0219 others(9): Show |
12 | HG00558.hp2 HG00738.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.84+112_84+147dupAG others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | G | GTACCATG others(47): Show |
3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0006c0009t0001g0191 |
3 | NA18960.hp2 NA19083.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.84+94_84+147dupAGC others(51): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | G | GTACCATG others(65): Show |
1 | a0002c0002t0008g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84+76_84+147dupAGC others(69): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | G | T | 261 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0088 others(258): Show |
276 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.84+148C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | GTACCATG others(11): Show |
G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0292 others(16): Show |
25 | HG00639.hp1 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.84+130_84+147delAG others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | GTACCATG others(29): Show |
G | 20 | a0001c0001t0001g0018 a0001c0001t0001g0305 a0001c0001t0001g0306 others(17): Show |
21 | HG00280.hp2 HG00597.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+112_84+147delAG others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | GTACCATG others(47): Show |
G | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0003t0001g0324 others(1): Show |
4 | HG00735.hp1 HG02976.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+94_84+147delAGC others(51): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712356 | GTACCATG others(65): Show |
G | 2 | a0001c0001t0001g0326 a0001c0003t0001g0325 |
2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.84+76_84+147delAGC others(69): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | |||||||
chr18:712365 | C | T | 1 | a0001c0001t0002g0023 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.84+139G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712365 | |||||||
chr18:712476 | CCGCGCTT others(10): Show |
C | 1 | a0001c0001t0001g0327 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.84+11_84+27delACGC others(13): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712476 |