Item | Value |
---|---|
geneid | 8863 |
ensemblid | ENSG00000049246.15 |
hgncid | 8847 |
symbol | PER3 |
name | period circadian regulator 3 |
refseq_nuc | NM_001377275.1 |
refseq_prot | NP_001364204.1 |
ensembl_nuc | ENST00000377532.8 |
ensembl_prot | ENSP00000366755.3 |
mane_status | MANE Select |
chr | chr1 |
start | 7784291 |
end | 7845177 |
strand | + |
ver | v1.2 |
region | chr1:7784291-7845177 |
region5000 | chr1:7779291-7850177 |
regionname0 | PER3_chr1_7784291_7845177 |
regionname5000 | PER3_chr1_7779291_7850177 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1192 | 228 | 49 | 31 | 129 | 5 | 14 | 101 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0002 | 0/0 | 1210 | 96 | 34 | 14 | 32 | 4 | 12 | 26 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0003 | 0/0 | 1192 | 32 | 4 | 13 | 7 | 3 | 5 | 7 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0004 | 0/0 | 1192 | 31 | 0 | 9 | 18 | 0 | 4 | 18 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0005 | 1/1 | 1210 | 8 | 2 | 2 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0006 | 0/0 | 1192 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0007 | 0/0 | 1192 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0008 | 0/0 | 1210 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0009 | 0/0 | 1210 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0010 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0011 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
a0012 | 0/0 | 1210 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0013 | 0/0 | 1210 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0014 | 0/0 | 1210 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1205): Show |
chr1 | 7779291 | 7850177 |
a0015 | 0/0 | 1192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | MPRGE others(1187): Show |
chr1 | 7779291 | 7850177 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3576 | 107 | 23 | 11 | 60 | 1 | 12 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0003 | 0/0 | 3576 | 57 | 0 | 14 | 42 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0004 | 0/0 | 3576 | 36 | 20 | 5 | 7 | 4 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0007 | 0/0 | 3576 | 14 | 0 | 0 | 13 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0009 | 0/0 | 3576 | 4 | 3 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0011 | 0/0 | 3576 | 4 | 0 | 0 | 4 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0016 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0018 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0019 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0021 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0027 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0001c0028 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0002c0002 | 0/0 | 3630 | 89 | 28 | 14 | 31 | 4 | 12 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0002c0012 | 0/0 | 3630 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0002c0013 | 0/0 | 3630 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0002c0020 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0003c0005 | 0/0 | 3576 | 32 | 4 | 13 | 7 | 3 | 5 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0004c0006 | 0/0 | 3576 | 31 | 0 | 9 | 18 | 0 | 4 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0005c0008 | 1/1 | 3630 | 7 | 1 | 2 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0005c0024 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0006c0010 | 0/0 | 3576 | 4 | 0 | 3 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0007c0014 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0008c0015 | 0/0 | 3630 | 2 | 1 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0009c0022 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0010c0023 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0011c0017 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 | ||
a0012c0025 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0013c0026 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0014c0029 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3625): Show |
chr1 | 7779291 | 7850177 | ||
a0015c0030 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | ATGCC others(3571): Show |
chr1 | 7779291 | 7850177 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6311 | 103 | 22 | 11 | 57 | 1 | 12 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0001t0008 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0001t0009 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0001t0013 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0001t0018 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0003t0001 | 0/0 | 6311 | 51 | 0 | 13 | 37 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0003t0004 | 0/0 | 6311 | 5 | 0 | 0 | 5 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0003t0016 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0004t0001 | 0/0 | 6311 | 17 | 5 | 2 | 7 | 3 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0004t0002 | 0/0 | 6311 | 15 | 13 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0004t0006 | 0/0 | 6311 | 3 | 1 | 1 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0004t0011 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0007t0001 | 0/0 | 6311 | 14 | 0 | 0 | 13 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0009t0001 | 0/0 | 6311 | 4 | 3 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0011t0001 | 0/0 | 6311 | 4 | 0 | 0 | 4 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0016t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0018t0001 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0019t0001 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0021t0005 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0027t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0001c0028t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0002c0002t0001 | 0/0 | 6365 | 88 | 27 | 14 | 31 | 4 | 12 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0002c0002t0012 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0002c0012t0001 | 0/0 | 6365 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0002c0013t0001 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0002c0013t0005 | 0/0 | 6365 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0002c0020t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0003c0005t0001 | 0/0 | 6311 | 29 | 4 | 12 | 7 | 1 | 5 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0003c0005t0007 | 0/0 | 6311 | 2 | 0 | 0 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0003c0005t0010 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0004c0006t0001 | 0/0 | 6311 | 30 | 0 | 8 | 18 | 0 | 4 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0004c0006t0015 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0005c0008t0003 | 1/1 | 6365 | 7 | 1 | 2 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0005c0024t0014 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0006c0010t0001 | 0/0 | 6311 | 4 | 0 | 3 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0007c0014t0001 | 0/0 | 6311 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0008c0015t0001 | 0/0 | 6365 | 2 | 1 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0009c0022t0001 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0010c0023t0001 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0011c0017t0017 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
a0012c0025t0001 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0013c0026t0005 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0014c0029t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6360): Show |
chr1 | 7779291 | 7850177 |
a0015c0030t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | GACCG others(6306): Show |
chr1 | 7779291 | 7850177 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0009g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0013g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0018g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0016g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0009t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0009t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0009t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0009t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0011t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0011t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0011t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0016t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0018t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0019t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0021t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0027t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0028t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0012t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0012t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0012t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0013t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0013t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0013t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0020t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0015g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0028 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0363 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0024t0014g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0007c0014t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0007c0014t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0008c0015t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0008c0015t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0009c0022t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0010c0023t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0011c0017t0017g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0012c0025t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0013c0026t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0014c0029t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0015c0030t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0168 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0162 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00140 | hp2 | a0005 | c0008 | t0003 | g0362 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00280 | hp1 | a0001 | c0004 | t0006 | g0160 | EUR | FIN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0210 | EUR | FIN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00423 | hp1 | a0001 | c0001 | t0009 | g0322 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00423 | hp2 | a0001 | c0007 | t0001 | g0253 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00544 | hp1 | a0001 | c0027 | t0001 | g0131 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00544 | hp2 | a0007 | c0014 | t0001 | g0365 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00621 | hp1 | a0001 | c0003 | t0004 | g0114 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00639 | hp2 | a0001 | c0004 | t0002 | g0164 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00642 | hp2 | a0004 | c0006 | t0001 | g0041 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00735 | hp1 | a0003 | c0005 | t0001 | g0091 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00735 | hp2 | a0004 | c0006 | t0015 | g0052 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00738 | hp1 | a0003 | c0005 | t0001 | g0089 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0030 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00741 | hp1 | a0006 | c0010 | t0001 | g0127 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00741 | hp2 | a0004 | c0006 | t0001 | g0039 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01069 | hp1 | a0004 | c0006 | t0001 | g0048 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01074 | hp1 | a0005 | c0008 | t0003 | g0361 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0136 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01106 | hp2 | a0003 | c0005 | t0001 | g0085 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01109 | hp1 | a0001 | c0004 | t0002 | g0171 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01109 | hp2 | a0004 | c0006 | t0001 | g0036 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01167 | hp1 | a0006 | c0010 | t0001 | g0130 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01167 | hp2 | a0005 | c0008 | t0003 | g0368 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01169 | hp2 | a0006 | c0010 | t0001 | g0133 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01175 | hp1 | a0003 | c0005 | t0010 | g0076 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01192 | hp2 | a0001 | c0003 | t0016 | g0121 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01243 | hp1 | a0008 | c0015 | t0001 | g0060 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01243 | hp2 | a0001 | c0009 | t0001 | g0302 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01255 | hp2 | a0003 | c0005 | t0001 | g0082 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0139 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0138 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01258 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01261 | hp2 | a0001 | c0004 | t0006 | g0159 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01346 | hp1 | a0004 | c0006 | t0001 | g0044 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01346 | hp2 | a0003 | c0005 | t0001 | g0010 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01361 | hp1 | a0003 | c0005 | t0001 | g0077 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0137 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01433 | hp1 | a0003 | c0005 | t0001 | g0010 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01433 | hp2 | a0004 | c0006 | t0001 | g0034 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0235 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01516 | hp1 | a0003 | c0005 | t0007 | g0090 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0165 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01517 | hp1 | a0003 | c0005 | t0007 | g0092 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0221 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0351 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01891 | hp1 | a0008 | c0015 | t0001 | g0059 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01934 | hp1 | a0009 | c0022 | t0001 | g0214 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0128 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0132 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01952 | hp2 | a0003 | c0005 | t0001 | g0075 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01975 | hp1 | a0003 | c0005 | t0001 | g0079 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01981 | hp1 | a0003 | c0005 | t0001 | g0078 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0145 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02055 | hp1 | a0002 | c0012 | t0001 | g0180 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02055 | hp2 | a0001 | c0021 | t0005 | g0096 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02056 | hp2 | a0001 | c0007 | t0001 | g0256 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02071 | hp2 | a0001 | c0003 | t0004 | g0109 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02083 | hp1 | a0001 | c0007 | t0001 | g0021 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02135 | hp1 | a0001 | c0003 | t0004 | g0107 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02135 | hp2 | a0001 | c0016 | t0001 | g0167 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0140 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02148 | hp2 | a0003 | c0005 | t0001 | g0093 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02165 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02257 | hp2 | a0010 | c0023 | t0001 | g0208 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02258 | hp2 | a0001 | c0004 | t0002 | g0174 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02280 | hp2 | a0001 | c0004 | t0002 | g0172 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02293 | hp2 | a0004 | c0006 | t0001 | g0031 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02451 | hp1 | a0001 | c0019 | t0001 | g0300 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02615 | hp1 | a0001 | c0004 | t0002 | g0169 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02622 | hp1 | a0011 | c0017 | t0017 | g0182 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0175 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0293 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02647 | hp1 | a0001 | c0004 | t0011 | g0064 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02647 | hp2 | a0012 | c0025 | t0001 | g0061 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02698 | hp2 | a0003 | c0005 | t0001 | g0080 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0224 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0294 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02886 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02886 | hp2 | a0005 | c0024 | t0014 | g0259 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02895 | hp1 | a0002 | c0013 | t0005 | g0097 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02895 | hp2 | a0003 | c0005 | t0001 | g0012 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02897 | hp2 | a0002 | c0013 | t0005 | g0098 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02970 | hp1 | a0013 | c0026 | t0005 | g0095 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02976 | hp1 | a0003 | c0005 | t0001 | g0158 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03017 | hp2 | a0003 | c0005 | t0001 | g0177 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0001 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03130 | hp1 | a0005 | c0008 | t0003 | g0367 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03139 | hp1 | a0002 | c0012 | t0001 | g0179 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03139 | hp2 | a0001 | c0004 | t0002 | g0170 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03195 | hp1 | a0001 | c0018 | t0001 | g0305 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03195 | hp2 | a0003 | c0005 | t0001 | g0012 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03225 | hp2 | a0001 | c0009 | t0001 | g0323 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03239 | hp2 | a0004 | c0006 | t0001 | g0035 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03453 | hp2 | a0001 | c0004 | t0002 | g0173 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03486 | hp1 | a0001 | c0009 | t0001 | g0290 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0292 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03490 | hp1 | a0004 | c0006 | t0001 | g0049 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03540 | hp2 | a0001 | c0009 | t0001 | g0317 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03654 | hp1 | a0004 | c0006 | t0001 | g0032 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0068 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03688 | hp1 | a0001 | c0007 | t0001 | g0022 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03831 | hp2 | a0004 | c0006 | t0001 | g0033 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03927 | hp2 | a0006 | c0010 | t0001 | g0102 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0240 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04184 | hp1 | a0003 | c0005 | t0001 | g0083 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04199 | hp2 | a0003 | c0005 | t0001 | g0086 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18522 | hp2 | a0001 | c0004 | t0002 | g0016 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18612 | hp1 | a0001 | c0007 | t0001 | g0021 | EAS | CHB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18612 | hp2 | a0007 | c0014 | t0001 | g0364 | EAS | CHB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18906 | hp1 | a0002 | c0012 | t0001 | g0178 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18941 | hp2 | a0004 | c0006 | t0001 | g0042 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18944 | hp1 | a0001 | c0007 | t0001 | g0261 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18945 | hp2 | a0004 | c0006 | t0001 | g0009 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18946 | hp1 | a0001 | c0004 | t0001 | g0166 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18948 | hp2 | a0004 | c0006 | t0001 | g0053 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18949 | hp2 | a0001 | c0004 | t0001 | g0161 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18950 | hp1 | a0004 | c0006 | t0001 | g0040 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18951 | hp1 | a0004 | c0006 | t0001 | g0057 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18951 | hp2 | a0001 | c0003 | t0004 | g0110 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18952 | hp1 | a0004 | c0006 | t0001 | g0054 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18952 | hp2 | a0001 | c0007 | t0001 | g0254 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18953 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18956 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18959 | hp1 | a0014 | c0029 | t0001 | g0239 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18962 | hp1 | a0003 | c0005 | t0001 | g0069 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18967 | hp1 | a0001 | c0028 | t0001 | g0347 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18968 | hp2 | a0003 | c0005 | t0001 | g0084 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18969 | hp2 | a0004 | c0006 | t0001 | g0045 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18970 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18971 | hp2 | a0003 | c0005 | t0001 | g0071 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18980 | hp2 | a0001 | c0011 | t0001 | g0320 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18982 | hp1 | a0001 | c0007 | t0001 | g0258 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18983 | hp1 | a0001 | c0007 | t0001 | g0022 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18984 | hp2 | a0001 | c0003 | t0004 | g0153 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18985 | hp2 | a0001 | c0007 | t0001 | g0205 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18989 | hp2 | a0004 | c0006 | t0001 | g0046 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18992 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18993 | hp1 | a0004 | c0006 | t0001 | g0009 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18994 | hp2 | a0015 | c0030 | t0001 | g0026 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18997 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18997 | hp2 | a0004 | c0006 | t0001 | g0037 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18998 | hp2 | a0004 | c0006 | t0001 | g0038 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19000 | hp1 | a0001 | c0007 | t0001 | g0250 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19002 | hp1 | a0004 | c0006 | t0001 | g0050 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19003 | hp1 | a0004 | c0006 | t0001 | g0047 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19003 | hp2 | a0001 | c0001 | t0013 | g0297 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19005 | hp1 | a0004 | c0006 | t0001 | g0055 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0125 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19011 | hp1 | a0001 | c0011 | t0001 | g0025 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19030 | hp1 | a0002 | c0002 | t0012 | g0201 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19055 | hp2 | a0003 | c0005 | t0001 | g0072 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19062 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19062 | hp2 | a0004 | c0006 | t0001 | g0056 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19063 | hp1 | a0004 | c0006 | t0001 | g0029 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19067 | hp2 | a0001 | c0007 | t0001 | g0252 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19068 | hp1 | a0004 | c0006 | t0001 | g0043 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19068 | hp2 | a0003 | c0005 | t0001 | g0073 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19070 | hp2 | a0003 | c0005 | t0001 | g0074 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19074 | hp1 | a0001 | c0011 | t0001 | g0330 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19076 | hp1 | a0002 | c0020 | t0001 | g0355 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19077 | hp1 | a0001 | c0007 | t0001 | g0251 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19077 | hp2 | a0004 | c0006 | t0001 | g0051 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19079 | hp1 | a0003 | c0005 | t0001 | g0070 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19079 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19082 | hp2 | a0001 | c0007 | t0001 | g0341 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19086 | hp1 | a0001 | c0011 | t0001 | g0025 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0016 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20752 | hp1 | a0003 | c0005 | t0001 | g0081 | EUR | TSI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20752 | hp2 | a0005 | c0008 | t0003 | g0028 | EUR | TSI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20905 | hp1 | a0003 | c0005 | t0001 | g0087 | SAS | GIH | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | GIH | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01123 | hp2 | a0003 | c0005 | t0001 | g0088 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02486 | hp1 | a0001 | c0004 | t0006 | g0163 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02559 | hp1 | a0002 | c0013 | t0001 | g0094 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0176 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG06807 | hp2 | a0003 | c0005 | t0001 | g0063 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
homoSapiens | chm13v2 | a0005 | c0008 | t0003 | g0028 | REF | REF | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
homoSapiens | grch38p0 | a0005 | c0008 | t0003 | g0363 | REF | REF | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7785533 | C | T | 1 | a0015 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.221C>T | p.Pro74Leu | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/22 | 531/6365 | 221/3633 | 74/1210 | chr1 | 7785533 | |||
chr1:7788142 | C | T | 1 | a0014 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.488C>T | p.Ala163Val | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/22 | 798/6365 | 488/3633 | 163/1210 | chr1 | 7788142 | |||
chr1:7809908 | G | A | 1 | a0011 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1258G>A | p.Val420Met | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/22 | 1568/6365 | 1258/3633 | 420/1210 | chr1 | 7809908 | |||
chr1:7820620 | A | G | 1 | a0012 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1937A>G | p.His646Arg | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/22 | 2247/6365 | 1937/3633 | 646/1210 | chr1 | 7820620 | |||
chr1:7820623 | T | G | 1 | a0003 | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
missense_variant | MODERATE | c.1940T>G | p.Val647Gly | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/22 | 2250/6365 | 1940/3633 | 647/1210 | chr1 | 7820623 | |||
chr1:7827174 | C | T | 1 | a0013 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2245C>T | p.Arg749Trp | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2555/6365 | 2245/3633 | 749/1210 | chr1 | 7827174 | |||
chr1:7827202 | G | A | 1 | a0006 | 4 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
missense_variant | MODERATE | c.2273G>A | p.Ser758Asn | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2583/6365 | 2273/3633 | 758/1210 | chr1 | 7827202 | |||
chr1:7827433 | T | C | 14 | a0001 a0002 a0003 others(11): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
missense_variant | MODERATE | c.2504T>C | p.Leu835Pro | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2814/6365 | 2504/3633 | 835/1210 | chr1 | 7827433 | |||
chr1:7827439 | T | G | 1 | a0008 | 2 | HG01243.hp1 HG01891.hp1 |
missense_variant | MODERATE | c.2510T>G | p.Leu837Trp | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2820/6365 | 2510/3633 | 837/1210 | chr1 | 7827439 | |||
chr1:7827519 | C | G | 1 | a0004 | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
missense_variant | MODERATE | c.2590C>G | p.Pro864Ala | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2900/6365 | 2590/3633 | 864/1210 | chr1 | 7827519 | |||
chr1:7827709 | C | T | 1 | a0007 | 2 | HG00544.hp2 NA18612.hp2 |
missense_variant | MODERATE | c.2780C>T | p.Ser927Leu | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 3090/6365 | 2780/3633 | 927/1210 | chr1 | 7827709 | |||
chr1:7829912 | GAGAATCC others(47): Show |
G | 7 | a0001 a0003 a0004 others(4): Show |
299 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(296): Show |
conservative_inframe_deletion | MODERATE | c.3046_3099delGCTCTG others(48): Show |
p.Ala1016_Ser1033del | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3356/6365 | 3046/3633 | 1016/1210 | INFO_REALIGN_3_PRIME | chr1 | 7829912 | ||
chr1:7830003 | CAGGATCG others(47): Show |
C | 1 | a0010 | 1 | HG02257.hp2 | disruptive_inframe_deletion | MODERATE | c.3057_3110delAGGATC others(48): Show |
p.Gly1020_Met1037del | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3367/6365 | 3057/3633 | 1019/1210 | chr1 | 7830003 | |||
chr1:7830057 | T | C | 3 | a0001 a0003 a0004 |
64 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(61): Show |
missense_variant | MODERATE | c.3110T>C | p.Met1037Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3420/6365 | 3110/3633 | 1037/1210 | chr1 | 7830057 | |||
chr1:7830063 | T | C | 1 | a0010 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.3116T>C | p.Leu1039Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3426/6365 | 3116/3633 | 1039/1210 | chr1 | 7830063 | |||
chr1:7835781 | A | G | 1 | a0001 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.3234A>G | p.Ile1078Met | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/22 | 3544/6365 | 3234/3633 | 1078/1210 | chr1 | 7835781 | |||
chr1:7835906 | C | T | 1 | a0009 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.3359C>T | p.Thr1120Ile | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/22 | 3669/6365 | 3359/3633 | 1120/1210 | chr1 | 7835906 | |||
chr1:7837073 | A | G | 1 | a0003 | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
missense_variant | MODERATE | c.3473A>G | p.His1158Arg | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/22 | 3783/6365 | 3473/3633 | 1158/1210 | chr1 | 7837073 | |||
chr1:7842676 | G | C | 1 | a0001 | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.3554G>C | p.Cys1185Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 3864/6365 | 3554/3633 | 1185/1210 | chr1 | 7842676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7785468 | T | G | 1 | a0001c0016 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.156T>G | p.Ser52Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/22 | 466/6365 | 156/3633 | 52/1210 | chr1 | 7785468 | |||
chr1:7785507 | C | T | 1 | a0001c0011 | 4 | NA18980.hp2 NA19011.hp1 NA19074.hp1 others(1): Show |
synonymous_variant | LOW | c.195C>T | p.Tyr65Tyr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/22 | 505/6365 | 195/3633 | 65/1210 | chr1 | 7785507 | |||
chr1:7794006 | C | T | 1 | a0001c0028 | 1 | NA18967.hp1 | splice_region_variant&synonymous_variant | LOW | c.642C>T | p.Ile214Ile | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/22 | 952/6365 | 642/3633 | 214/1210 | chr1 | 7794006 | |||
chr1:7809988 | T | C | 26 | a0001c0001 a0001c0004 a0001c0007 others(23): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.1338T>C | p.Ser446Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/22 | 1648/6365 | 1338/3633 | 446/1210 | chr1 | 7809988 | |||
chr1:7820525 | A | T | 2 | a0002c0013 a0013c0026 |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.1842A>T | p.Ile614Ile | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/22 | 2152/6365 | 1842/3633 | 614/1210 | chr1 | 7820525 | |||
chr1:7827188 | G | A | 16 | a0001c0001 a0001c0003 a0001c0004 others(13): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
synonymous_variant | LOW | c.2259G>A | p.Pro753Pro | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2569/6365 | 2259/3633 | 753/1210 | chr1 | 7827188 | |||
chr1:7827344 | C | T | 1 | a0001c0007 | 14 | HG00423.hp2 HG02056.hp2 HG02083.hp1 others(11): Show |
synonymous_variant | LOW | c.2415C>T | p.Tyr805Tyr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2725/6365 | 2415/3633 | 805/1210 | chr1 | 7827344 | |||
chr1:7827413 | A | G | 1 | a0001c0027 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.2484A>G | p.Ala828Ala | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2794/6365 | 2484/3633 | 828/1210 | chr1 | 7827413 | |||
chr1:7827545 | G | A | 3 | a0001c0003 a0001c0027 a0006c0010 |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
synonymous_variant | LOW | c.2616G>A | p.Ser872Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2926/6365 | 2616/3633 | 872/1210 | chr1 | 7827545 | |||
chr1:7829881 | C | T | 10 | a0001c0001 a0001c0007 a0001c0009 others(7): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
synonymous_variant | LOW | c.2934C>T | p.Thr978Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3244/6365 | 2934/3633 | 978/1210 | chr1 | 7829881 | |||
chr1:7829887 | A | G | 1 | a0002c0012 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2940A>G | p.Ala980Ala | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3250/6365 | 2940/3633 | 980/1210 | chr1 | 7829887 | |||
chr1:7830004 | A | G | 6 | a0002c0002 a0005c0024 a0008c0015 others(3): Show |
93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
synonymous_variant | LOW | c.3057A>G | p.Thr1019Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3367/6365 | 3057/3633 | 1019/1210 | chr1 | 7830004 | |||
chr1:7830112 | G | T | 1 | a0001c0019 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3165G>T | p.Thr1055Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3475/6365 | 3165/3633 | 1055/1210 | chr1 | 7830112 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7784731 | C | T | 1 | a0001c0001t0018 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/22 | 147 | chr1 | 7784731 | ||||||
chr1:7784740 | C | T | 1 | a0011c0017t0017 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-138C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/22 | chr1 | 7784740 | |||||||
chr1:7784794 | G | A | 3 | a0001c0021t0005 a0002c0013t0005 a0013c0026t0005 |
4 | HG02055.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-84G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/22 | 84 | chr1 | 7784794 | ||||||
chr1:7842793 | C | T | 1 | a0001c0003t0016 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 38 | chr1 | 7842793 | ||||||
chr1:7843186 | A | G | 1 | a0004c0006t0015 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*431A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 431 | chr1 | 7843186 | ||||||
chr1:7843511 | C | T | 1 | a0005c0024t0014 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 756 | chr1 | 7843511 | ||||||
chr1:7843534 | A | T | 1 | a0001c0001t0013 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 779 | chr1 | 7843534 | ||||||
chr1:7843778 | G | A | 1 | a0001c0004t0002 | 15 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1023G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1023 | chr1 | 7843778 | ||||||
chr1:7844069 | G | T | 1 | a0002c0002t0012 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1314 | chr1 | 7844069 | ||||||
chr1:7844123 | C | T | 1 | a0001c0004t0011 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1368C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1368 | chr1 | 7844123 | ||||||
chr1:7844136 | A | G | 1 | a0003c0005t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1381 | chr1 | 7844136 | ||||||
chr1:7844175 | C | T | 1 | a0001c0003t0004 | 5 | HG00621.hp1 HG02071.hp2 HG02135.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1420 | chr1 | 7844175 | ||||||
chr1:7844187 | C | T | 43 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(40): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
3_prime_UTR_variant | MODIFIER | c.*1432C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1432 | chr1 | 7844187 | ||||||
chr1:7844415 | G | A | 43 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(40): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
3_prime_UTR_variant | MODIFIER | c.*1660G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1660 | chr1 | 7844415 | ||||||
chr1:7844639 | C | T | 1 | a0001c0004t0006 | 3 | HG00280.hp1 HG01261.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1884C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1884 | chr1 | 7844639 | ||||||
chr1:7844820 | C | T | 1 | a0005c0024t0014 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2065 | chr1 | 7844820 | ||||||
chr1:7844920 | G | T | 1 | a0003c0005t0007 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2165G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2165 | chr1 | 7844920 | ||||||
chr1:7845050 | C | T | 1 | a0001c0001t0009 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2295 | chr1 | 7845050 | ||||||
chr1:7845161 | G | A | 1 | a0001c0001t0008 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2406G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2406 | chr1 | 7845161 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7784381 | GTGCGCGG others(14): Show |
G | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG00673.hp2 HG01070.hp1 |
splice_region_variant&intron_variant | LOW | c.-225+8_-225+28delC others(20): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 7784381 | ||||||
chr1:7784383 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
123 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.-225+7G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784383 | |||||||
chr1:7784384 | C | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
123 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.-225+8C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784384 | |||||||
chr1:7784384 | CGCGGCCG others(14): Show |
C | 3 | a0002c0002t0001g0020 a0002c0002t0001g0202 a0012c0025t0001g0061 |
3 | HG02647.hp2 NA18989.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-225+32_-225+52del others(21): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 7784384 | ||||||
chr1:7784404 | G | T | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG00673.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-225+28G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784404 | |||||||
chr1:7784405 | G | A | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG00673.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-225+29G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784405 | |||||||
chr1:7784409 | G | A | 30 | a0004c0006t0001g0009 a0004c0006t0001g0029 a0004c0006t0001g0030 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-225+33G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784409 | |||||||
chr1:7784471 | A | C | 1 | a0001c0001t0001g0369 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-225+95A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784471 | |||||||
chr1:7784620 | T | C | 258 | a0001c0001t0001g0181 a0001c0001t0001g0255 a0001c0001t0001g0257 others(255): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-224-34T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784620 | |||||||
chr1:7784648 | C | T | 2 | a0005c0008t0003g0367 a0005c0008t0003g0368 |
2 | HG01167.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.-224-6C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784648 | |||||||
chr1:7785027 | G | A | 19 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(16): Show |
19 | HG00438.hp2 HG00558.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.128+22G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785027 | |||||||
chr1:7785157 | G | A | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.128+152G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785157 | |||||||
chr1:7785312 | G | T | 1 | a0001c0001t0001g0366 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.129-129G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785312 | |||||||
chr1:7785333 | T | C | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.129-108T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785333 | |||||||
chr1:7785353 | A | G | 1 | a0002c0002t0001g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.129-88A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785353 | |||||||
chr1:7785635 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
299 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.274+49T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785635 | |||||||
chr1:7785686 | G | C | 4 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+100G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785686 | |||||||
chr1:7785716 | G | A | 1 | a0004c0006t0001g0029 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.274+130G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785716 | |||||||
chr1:7785725 | C | T | 2 | a0002c0002t0001g0184 a0002c0002t0001g0185 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.274+139C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785725 | |||||||
chr1:7785765 | A | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.274+179A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785765 | |||||||
chr1:7785890 | T | G | 1 | a0001c0004t0001g0062 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.274+304T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785890 | |||||||
chr1:7785986 | G | A | 2 | a0002c0002t0001g0017 a0002c0002t0001g0189 |
3 | HG00733.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.274+400G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785986 | |||||||
chr1:7786005 | C | G | 1 | a0001c0001t0001g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274+419C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786005 | |||||||
chr1:7786032 | A | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.274+446A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786032 | |||||||
chr1:7786086 | C | T | 60 | a0001c0003t0001g0011 a0001c0003t0001g0099 a0001c0003t0001g0100 others(57): Show |
61 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.274+500C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786086 | |||||||
chr1:7786197 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-524G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786197 | |||||||
chr1:7786209 | C | T | 5 | a0001c0021t0005g0096 a0002c0013t0001g0094 a0002c0013t0005g0097 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-512C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786209 | |||||||
chr1:7786210 | A | G | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.275-511A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786210 | |||||||
chr1:7786225 | C | A | 1 | a0001c0009t0001g0290 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275-496C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786225 | |||||||
chr1:7786241 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.275-480C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786241 | |||||||
chr1:7786246 | C | G | 26 | a0003c0005t0001g0010 a0003c0005t0001g0069 a0003c0005t0001g0070 others(23): Show |
27 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.275-475C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786246 | |||||||
chr1:7786247 | T | A | 26 | a0003c0005t0001g0010 a0003c0005t0001g0069 a0003c0005t0001g0070 others(23): Show |
27 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.275-474T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786247 | |||||||
chr1:7786285 | T | C | 4 | a0003c0005t0001g0012 a0003c0005t0001g0158 a0008c0015t0001g0059 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-436T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786285 | |||||||
chr1:7786447 | C | T | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0002c0002t0001g0183 |
3 | HG03209.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.275-274C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786447 | |||||||
chr1:7786467 | A | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.275-254A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786467 | |||||||
chr1:7786477 | TTTAG | T | 30 | a0004c0006t0001g0009 a0004c0006t0001g0029 a0004c0006t0001g0030 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.275-238_275-235del others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 7786477 | ||||||
chr1:7786658 | G | A | 1 | a0003c0005t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.275-63G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786658 | |||||||
chr1:7786659 | A | G | 1 | a0003c0005t0001g0093 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.275-62A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786659 | |||||||
chr1:7786940 | A | G | 4 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0267 others(1): Show |
5 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+104A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7786940 | |||||||
chr1:7787003 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.390+167A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787003 | |||||||
chr1:7787072 | G | A | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+236G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787072 | |||||||
chr1:7787165 | C | T | 19 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(16): Show |
19 | HG00438.hp2 HG00558.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.390+329C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787165 | |||||||
chr1:7787166 | G | A | 15 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(12): Show |
16 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.390+330G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787166 | |||||||
chr1:7787302 | C | CT | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(356): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.390+472dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 7787302 | ||||||
chr1:7787355 | C | T | 1 | a0011c0017t0017g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.390+519C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787355 | |||||||
chr1:7787420 | C | T | 2 | a0002c0002t0001g0264 a0002c0002t0001g0265 |
2 | NA18957.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.390+584C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787420 | |||||||
chr1:7787469 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
126 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.391-576A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787469 | |||||||
chr1:7787471 | A | G | 1 | a0001c0003t0001g0157 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.391-574A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787471 | |||||||
chr1:7787554 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.391-491G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787554 | |||||||
chr1:7787640 | A | T | 4 | a0003c0005t0001g0012 a0003c0005t0001g0158 a0008c0015t0001g0059 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-405A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787640 | |||||||
chr1:7787707 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391-338G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787707 | |||||||
chr1:7787776 | T | C | 219 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0003t0001g0011 others(216): Show |
231 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.391-269T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787776 | |||||||
chr1:7787786 | G | A | 24 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(21): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.391-259G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787786 | |||||||
chr1:7787903 | G | C | 4 | a0003c0005t0001g0012 a0003c0005t0001g0158 a0008c0015t0001g0059 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-142G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787903 | |||||||
chr1:7788273 | A | G | 2 | a0002c0002t0001g0262 a0002c0002t0001g0263 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.592+27A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788273 | |||||||
chr1:7788350 | A | G | 1 | a0004c0006t0001g0057 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.592+104A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788350 | |||||||
chr1:7788372 | T | C | 1 | a0001c0007t0001g0205 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.592+126T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788372 | |||||||
chr1:7788497 | G | A | 78 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(75): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.592+251G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788497 | |||||||
chr1:7788527 | G | C | 1 | a0002c0013t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.592+281G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788527 | |||||||
chr1:7788551 | T | G | 2 | a0002c0002t0001g0018 a0002c0002t0001g0206 |
3 | HG00099.hp2 HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.592+305T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788551 | |||||||
chr1:7788556 | GT | G | 65 | a0001c0021t0005g0096 a0002c0012t0001g0178 a0002c0012t0001g0179 others(62): Show |
67 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.592+315delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788556 | ||||||
chr1:7788632 | G | A | 27 | a0003c0005t0001g0010 a0003c0005t0001g0063 a0003c0005t0001g0069 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.592+386G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788632 | |||||||
chr1:7788664 | G | T | 1 | a0001c0001t0001g0360 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+418G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788664 | |||||||
chr1:7788740 | C | T | 1 | a0001c0003t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.592+494C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788740 | |||||||
chr1:7788768 | G | A | 27 | a0003c0005t0001g0010 a0003c0005t0001g0063 a0003c0005t0001g0069 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.592+522G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788768 | |||||||
chr1:7788863 | C | A | 1 | a0001c0001t0001g0360 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+617C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788863 | |||||||
chr1:7788883 | G | A | 30 | a0004c0006t0001g0009 a0004c0006t0001g0029 a0004c0006t0001g0030 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+637G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788883 | |||||||
chr1:7788903 | T | TG | 5 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(2): Show |
5 | HG02129.hp2 NA19007.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+661dupG | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788903 | ||||||
chr1:7788907 | G | GA | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
137 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.592+678dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | ||||||
chr1:7788907 | G | GAA | 10 | a0001c0001t0001g0291 a0001c0003t0001g0154 a0001c0003t0001g0157 others(7): Show |
10 | NA18948.hp1 NA18962.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.592+677_592+678dup others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | ||||||
chr1:7788907 | G | GAAA | 57 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(54): Show |
58 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.592+676_592+678dup others(3): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | ||||||
chr1:7788907 | GA | G | 92 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(89): Show |
101 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.592+678delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | ||||||
chr1:7788924 | A | AT | 30 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+680dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788924 | ||||||
chr1:7788924 | A | T | 2 | a0004c0006t0001g0055 a0004c0006t0001g0056 |
2 | NA19005.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.592+678A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788924 | |||||||
chr1:7788940 | CTCTTACA others(5): Show |
C | 1 | a0002c0002t0001g0188 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.592+699_592+710del others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788940 | ||||||
chr1:7789140 | A | AAT | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
128 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.592+911_592+912dup others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789140 | A | AATAT | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0003t0001g0099 |
3 | HG02165.hp1 HG03831.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.592+909_592+912dup others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789140 | A | AATATAT | 12 | a0001c0004t0001g0023 a0001c0004t0001g0294 a0001c0004t0011g0064 others(9): Show |
14 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.592+907_592+912dup others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789140 | A | AATATATA others(1): Show |
11 | a0001c0004t0001g0292 a0001c0004t0001g0293 a0001c0004t0002g0001 others(8): Show |
15 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.592+905_592+912dup others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789140 | A | AATATATA others(3): Show |
10 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(7): Show |
13 | HG00099.hp1 HG00639.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+903_592+912dup others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789140 | A | AATATATA others(5): Show |
4 | a0001c0004t0001g0062 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG00140.hp1 HG02155.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+901_592+912dup others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789140 | A | AATATATA others(7): Show |
2 | a0001c0004t0006g0159 a0001c0004t0006g0160 |
2 | HG00280.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.592+899_592+912dup others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | ||||||
chr1:7789145 | A | ATG | 95 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(92): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592+900_592+901ins others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789145 | ||||||
chr1:7789145 | A | G | 1 | a0004c0006t0001g0054 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.592+899A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789145 | |||||||
chr1:7789163 | G | A | 3 | a0002c0012t0001g0178 a0005c0008t0003g0367 a0005c0008t0003g0368 |
3 | HG01167.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.592+917G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789163 | |||||||
chr1:7789195 | TA | T | 33 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 others(30): Show |
34 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.592+959delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789195 | ||||||
chr1:7789435 | T | G | 1 | a0001c0004t0001g0161 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.592+1189T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789435 | |||||||
chr1:7789452 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.592+1206C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789452 | |||||||
chr1:7789494 | G | A | 1 | a0002c0012t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.592+1248G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789494 | |||||||
chr1:7789596 | A | G | 100 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(97): Show |
109 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.592+1350A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789596 | |||||||
chr1:7789598 | C | A | 4 | a0001c0021t0005g0096 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+1352C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789598 | |||||||
chr1:7789722 | T | G | 1 | a0001c0001t0001g0360 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+1476T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789722 | |||||||
chr1:7789768 | C | G | 1 | a0001c0001t0001g0360 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+1522C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789768 | |||||||
chr1:7789781 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0337 a0001c0001t0001g0338 others(18): Show |
23 | HG00673.hp2 HG01952.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+1535C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789781 | |||||||
chr1:7789820 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
122 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.592+1574A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789820 | |||||||
chr1:7789840 | ATGTCATC others(6): Show |
A | 1 | a0001c0004t0002g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592+1597_592+1609d others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789840 | ||||||
chr1:7790002 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.592+1756C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790002 | |||||||
chr1:7790021 | C | T | 95 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(92): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592+1775C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790021 | |||||||
chr1:7790107 | C | T | 1 | a0001c0007t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.592+1861C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790107 | |||||||
chr1:7790111 | G | A | 1 | a0003c0005t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1865G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790111 | |||||||
chr1:7790158 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.592+1912C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790158 | |||||||
chr1:7790166 | C | T | 1 | a0001c0003t0001g0155 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.592+1920C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790166 | |||||||
chr1:7790359 | G | A | 1 | a0002c0020t0001g0355 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.592+2113G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790359 | |||||||
chr1:7790405 | C | T | 1 | a0002c0002t0001g0266 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.592+2159C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790405 | |||||||
chr1:7790463 | C | T | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.592+2217C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790463 | |||||||
chr1:7790540 | A | G | 4 | a0003c0005t0001g0012 a0003c0005t0001g0158 a0008c0015t0001g0059 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+2294A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790540 | |||||||
chr1:7790561 | C | G | 2 | a0003c0005t0001g0012 a0003c0005t0001g0158 |
3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.592+2315C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790561 | |||||||
chr1:7790750 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.592+2504C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790750 | |||||||
chr1:7790794 | T | A | 1 | a0002c0002t0001g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.592+2548T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790794 | |||||||
chr1:7790798 | CA | C | 4 | a0003c0005t0001g0012 a0003c0005t0001g0158 a0008c0015t0001g0059 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+2556delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7790798 | ||||||
chr1:7790830 | C | T | 1 | a0002c0002t0012g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.592+2584C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790830 | |||||||
chr1:7790838 | C | T | 24 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(21): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.592+2592C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790838 | |||||||
chr1:7791033 | C | T | 95 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(92): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592+2787C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791033 | |||||||
chr1:7791138 | C | T | 1 | a0001c0001t0001g0349 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.593-2819C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791138 | |||||||
chr1:7791198 | CT | C | 26 | a0003c0005t0001g0010 a0003c0005t0001g0069 a0003c0005t0001g0070 others(23): Show |
27 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.593-2758delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791198 | |||||||
chr1:7791332 | G | A | 1 | a0011c0017t0017g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.593-2625G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791332 | |||||||
chr1:7791407 | G | A | 1 | a0001c0003t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.593-2550G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791407 | |||||||
chr1:7791485 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0298 a0001c0001t0001g0335 others(4): Show |
9 | HG00558.hp1 HG02080.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-2472G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791485 | |||||||
chr1:7791577 | C | T | 60 | a0001c0003t0001g0011 a0001c0003t0001g0099 a0001c0003t0001g0100 others(57): Show |
61 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.593-2380C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791577 | |||||||
chr1:7791594 | A | C | 5 | a0001c0021t0005g0096 a0002c0013t0001g0094 a0002c0013t0005g0097 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-2363A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791594 | |||||||
chr1:7791680 | T | C | 1 | a0006c0010t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.593-2277T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791680 | |||||||
chr1:7791748 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.593-2209C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791748 | |||||||
chr1:7791792 | G | A | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.593-2165G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791792 | |||||||
chr1:7791860 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.593-2097G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791860 | |||||||
chr1:7791993 | A | C | 1 | a0001c0003t0001g0152 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.593-1964A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791993 | |||||||
chr1:7792057 | C | G | 30 | a0004c0006t0001g0009 a0004c0006t0001g0029 a0004c0006t0001g0030 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1900C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792057 | |||||||
chr1:7792069 | T | C | 27 | a0003c0005t0001g0010 a0003c0005t0001g0063 a0003c0005t0001g0069 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1888T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792069 | |||||||
chr1:7792132 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.593-1825T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792132 | |||||||
chr1:7792299 | AACTC | A | 6 | a0004c0006t0001g0031 a0004c0006t0001g0032 a0004c0006t0001g0033 others(3): Show |
6 | HG01109.hp2 HG01433.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-1654_593-1651d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7792299 | ||||||
chr1:7792311 | C | T | 15 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(12): Show |
16 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.593-1646C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792311 | |||||||
chr1:7792330 | A | G | 1 | a0002c0002t0001g0260 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.593-1627A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792330 | |||||||
chr1:7792375 | CAT | C | 6 | a0001c0004t0002g0016 a0001c0004t0002g0174 a0001c0004t0002g0175 others(3): Show |
7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-1581_593-1580d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792375 | |||||||
chr1:7792417 | G | A | 15 | a0001c0003t0001g0103 a0001c0003t0001g0104 a0001c0003t0001g0105 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.593-1540G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792417 | |||||||
chr1:7792507 | A | G | 5 | a0001c0021t0005g0096 a0002c0013t0001g0094 a0002c0013t0005g0097 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-1450A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792507 | |||||||
chr1:7792517 | A | G | 1 | a0004c0006t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.593-1440A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792517 | |||||||
chr1:7792630 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.593-1327C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792630 | |||||||
chr1:7792705 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.593-1252C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792705 | |||||||
chr1:7792737 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.593-1220C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792737 | |||||||
chr1:7792851 | G | A | 4 | a0003c0005t0001g0012 a0003c0005t0001g0158 a0008c0015t0001g0059 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1106G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792851 | |||||||
chr1:7792859 | T | C | 27 | a0003c0005t0001g0010 a0003c0005t0001g0063 a0003c0005t0001g0069 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1098T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792859 | |||||||
chr1:7792919 | T | G | 2 | a0004c0006t0001g0037 a0004c0006t0001g0038 |
2 | NA18997.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.593-1038T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792919 | |||||||
chr1:7793089 | T | G | 1 | a0001c0019t0001g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.593-868T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793089 | |||||||
chr1:7793143 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.593-814C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793143 | |||||||
chr1:7793532 | T | C | 67 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(64): Show |
68 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.593-425T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793532 | |||||||
chr1:7793540 | C | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.593-417C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793540 | |||||||
chr1:7793659 | C | G | 1 | a0004c0006t0015g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.593-298C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793659 | |||||||
chr1:7793692 | T | C | 1 | a0013c0026t0005g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.593-265T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793692 | |||||||
chr1:7793695 | G | T | 1 | a0001c0001t0001g0371 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.593-262G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793695 | |||||||
chr1:7793752 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.593-205G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793752 | |||||||
chr1:7793780 | T | A | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.593-177T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793780 | |||||||
chr1:7794105 | T | A | 5 | a0001c0021t0005g0096 a0002c0013t0001g0094 a0002c0013t0005g0097 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+97T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794105 | |||||||
chr1:7794145 | A | G | 1 | a0004c0006t0001g0036 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.644+137A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794145 | |||||||
chr1:7794149 | C | T | 27 | a0003c0005t0001g0010 a0003c0005t0001g0063 a0003c0005t0001g0069 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.644+141C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794149 | |||||||
chr1:7794270 | G | A | 15 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(12): Show |
16 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.644+262G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794270 | |||||||
chr1:7794290 | C | A | 1 | a0001c0001t0001g0356 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.644+282C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794290 | |||||||
chr1:7794391 | G | A | 1 | a0001c0009t0001g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.644+383G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794391 | |||||||
chr1:7794479 | G | A | 4 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0184 others(1): Show |
4 | HG02717.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+471G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794479 | |||||||
chr1:7794495 | A | G | 38 | a0001c0021t0005g0096 a0002c0012t0001g0178 a0002c0012t0001g0179 others(35): Show |
39 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.644+487A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794495 | |||||||
chr1:7794603 | A | G | 1 | a0001c0009t0001g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.644+595A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794603 | |||||||
chr1:7794686 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.644+678G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794686 | |||||||
chr1:7794903 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.644+895A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794903 | |||||||
chr1:7794938 | G | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.644+930G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794938 | |||||||
chr1:7795001 | A | G | 1 | a0002c0002t0001g0183 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.644+993A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795001 | |||||||
chr1:7795101 | G | A | 4 | a0001c0004t0002g0016 a0001c0004t0002g0174 a0001c0004t0002g0175 others(1): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+1093G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795101 | |||||||
chr1:7795322 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0337 a0001c0001t0001g0338 others(10): Show |
15 | HG02056.hp1 HG02129.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.644+1314G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795322 | |||||||
chr1:7795361 | T | G | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.644+1353T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795361 | |||||||
chr1:7795375 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.644+1367A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795375 | |||||||
chr1:7795375 | A | T | 2 | a0003c0005t0001g0012 a0003c0005t0001g0158 |
3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.644+1367A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795375 | |||||||
chr1:7795423 | G | A | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.644+1415G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795423 | |||||||
chr1:7795434 | G | A | 77 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0007t0001g0021 others(74): Show |
85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.644+1426G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795434 | |||||||
chr1:7795448 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.644+1440G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795448 | |||||||
chr1:7795516 | C | T | 2 | a0003c0005t0001g0012 a0003c0005t0001g0158 |
3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.644+1508C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795516 | |||||||
chr1:7795650 | A | G | 1 | a0008c0015t0001g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.644+1642A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795650 | |||||||
chr1:7795673 | G | A | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.644+1665G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795673 | |||||||
chr1:7795682 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(11): Show |
15 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.644+1674C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795682 | |||||||
chr1:7795721 | G | A | 1 | a0002c0002t0012g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.644+1713G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795721 | |||||||
chr1:7795754 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.644+1746A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795754 | |||||||
chr1:7795850 | C | T | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.644+1842C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795850 | |||||||
chr1:7795921 | C | T | 1 | a0001c0003t0001g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.644+1913C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795921 | |||||||
chr1:7796080 | C | T | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.644+2072C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796080 | |||||||
chr1:7796206 | G | C | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.644+2198G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796206 | |||||||
chr1:7796207 | C | A | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.644+2199C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796207 | |||||||
chr1:7796286 | T | C | 118 | a0001c0004t0011g0064 a0001c0021t0005g0096 a0002c0002t0001g0002 others(115): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.645-2239T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796286 | |||||||
chr1:7796319 | C | CT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
139 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.645-2189dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | C | CTTT | 57 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(54): Show |
58 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.645-2191_645-2189d others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | C | CTTTTTT | 26 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(23): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.645-2194_645-2189d others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | C | CTTTTTTT others(1): Show |
79 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0018 others(76): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.645-2196_645-2189d others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | C | CTTTTTTT others(2): Show |
21 | a0002c0002t0001g0191 a0002c0002t0001g0203 a0002c0002t0001g0238 others(18): Show |
21 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.645-2197_645-2189d others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | C | CTTTTTTT others(3): Show |
8 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0192 others(5): Show |
9 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.645-2198_645-2189d others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | C | CTTTTTTT others(4): Show |
2 | a0002c0002t0001g0195 a0002c0002t0001g0268 |
2 | HG02572.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.645-2199_645-2189d others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796319 | CTT | C | 6 | a0001c0004t0011g0064 a0002c0002t0001g0065 a0002c0002t0001g0066 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-2190_645-2189d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | ||||||
chr1:7796444 | A | G | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.645-2081A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796444 | |||||||
chr1:7796476 | A | G | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.645-2049A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796476 | |||||||
chr1:7796514 | C | T | 2 | a0001c0007t0001g0258 a0001c0007t0001g0261 |
2 | NA18944.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.645-2011C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796514 | |||||||
chr1:7796709 | C | T | 1 | a0004c0006t0001g0030 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.645-1816C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796709 | |||||||
chr1:7796748 | G | A | 1 | a0002c0012t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.645-1777G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796748 | |||||||
chr1:7796906 | C | G | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.645-1619C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796906 | |||||||
chr1:7797188 | GTGTGAGC others(5): Show |
G | 210 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(207): Show |
221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.645-1320_645-1309d others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7797188 | ||||||
chr1:7797249 | G | A | 24 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(21): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.645-1276G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797249 | |||||||
chr1:7797314 | G | C | 13 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(10): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.645-1211G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797314 | |||||||
chr1:7797372 | C | T | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.645-1153C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797372 | |||||||
chr1:7797466 | C | G | 2 | a0002c0002t0001g0236 a0002c0002t0001g0237 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.645-1059C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797466 | |||||||
chr1:7797636 | T | TA | 55 | a0001c0003t0001g0068 a0001c0003t0001g0099 a0001c0003t0001g0100 others(52): Show |
55 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.645-873dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7797636 | ||||||
chr1:7797636 | TA | T | 28 | a0001c0001t0001g0332 a0001c0001t0001g0369 a0001c0004t0001g0168 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.645-873delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7797636 | ||||||
chr1:7797645 | A | AG | 4 | a0001c0003t0001g0011 a0001c0003t0001g0116 a0001c0003t0001g0149 others(1): Show |
5 | NA18956.hp2 NA18957.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-880_645-879ins others(1): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797645 | |||||||
chr1:7797645 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.645-880A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797645 | |||||||
chr1:7797646 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0334 |
2 | HG00408.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.645-879A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797646 | |||||||
chr1:7797718 | A | G | 1 | a0004c0006t0001g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.645-807A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797718 | |||||||
chr1:7797848 | G | A | 1 | a0001c0004t0001g0023 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.645-677G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797848 | |||||||
chr1:7797872 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.645-653C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797872 | |||||||
chr1:7797914 | C | T | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.645-611C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797914 | |||||||
chr1:7797948 | G | A | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.645-577G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797948 | |||||||
chr1:7798048 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.645-477A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798048 | |||||||
chr1:7798075 | G | C | 29 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(26): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.645-450G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798075 | |||||||
chr1:7798112 | G | A | 1 | a0001c0004t0001g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.645-413G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798112 | |||||||
chr1:7798226 | G | C | 1 | a0001c0001t0013g0297 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.645-299G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798226 | |||||||
chr1:7798739 | G | A | 1 | a0002c0002t0001g0263 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793+66G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7798739 | |||||||
chr1:7798865 | T | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.793+192T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7798865 | |||||||
chr1:7799131 | A | C | 69 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(66): Show |
70 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.793+458A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799131 | |||||||
chr1:7799257 | G | A | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.793+584G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799257 | |||||||
chr1:7799260 | C | G | 148 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0017 others(145): Show |
158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.793+587C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799260 | |||||||
chr1:7799419 | G | A | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+746G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799419 | |||||||
chr1:7799604 | C | CT | 148 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0017 others(145): Show |
158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.793+932dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799604 | ||||||
chr1:7799610 | C | CA | 17 | a0001c0001t0001g0344 a0001c0003t0001g0103 a0001c0003t0001g0122 others(14): Show |
21 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.793+957dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799610 | ||||||
chr1:7799610 | CA | C | 152 | a0001c0001t0001g0027 a0001c0001t0001g0282 a0001c0001t0001g0287 others(149): Show |
162 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.793+957delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799610 | ||||||
chr1:7799925 | C | T | 1 | a0004c0006t0001g0030 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.794-1188C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799925 | |||||||
chr1:7799936 | T | TTTTA | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1161_794-1158d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799936 | ||||||
chr1:7800047 | G | A | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.794-1066G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800047 | |||||||
chr1:7800157 | C | T | 1 | a0001c0016t0001g0167 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.794-956C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800157 | |||||||
chr1:7800216 | A | AT | 78 | a0001c0003t0004g0114 a0001c0021t0005g0096 a0002c0002t0001g0017 others(75): Show |
82 | HG00621.hp1 HG00642.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.794-886dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7800216 | ||||||
chr1:7800216 | AT | A | 26 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(23): Show |
33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.794-886delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7800216 | ||||||
chr1:7800320 | G | T | 148 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0017 others(145): Show |
158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.794-793G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800320 | |||||||
chr1:7800332 | C | T | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.794-781C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800332 | |||||||
chr1:7800487 | C | T | 3 | a0002c0013t0005g0097 a0002c0013t0005g0098 a0013c0026t0005g0095 |
3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.794-626C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800487 | |||||||
chr1:7800488 | G | A | 2 | a0001c0003t0001g0099 a0001c0003t0001g0156 |
2 | NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.794-625G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800488 | |||||||
chr1:7800553 | C | A | 1 | a0001c0001t0001g0024 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.794-560C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800553 | |||||||
chr1:7800691 | G | A | 1 | a0004c0006t0015g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.794-422G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800691 | |||||||
chr1:7800699 | C | T | 1 | a0001c0003t0001g0146 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.794-414C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800699 | |||||||
chr1:7800827 | C | CA | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.794-271dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7800827 | ||||||
chr1:7800841 | A | AG | 148 | a0001c0004t0011g0064 a0001c0021t0005g0096 a0002c0002t0001g0002 others(145): Show |
158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.794-272_794-271ins others(1): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800841 | |||||||
chr1:7801008 | A | G | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.794-105A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7801008 | |||||||
chr1:7801093 | C | CT | 147 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0017 others(144): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.794-17dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7801093 | ||||||
chr1:7801098 | T | G | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.794-15T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7801098 | |||||||
chr1:7801230 | A | G | 1 | a0005c0024t0014g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.872+39A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801230 | |||||||
chr1:7801244 | T | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.872+53T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801244 | |||||||
chr1:7801285 | G | A | 210 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(207): Show |
221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.872+94G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801285 | |||||||
chr1:7801458 | T | C | 1 | a0001c0004t0001g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.872+267T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801458 | |||||||
chr1:7801540 | C | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.872+349C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801540 | |||||||
chr1:7801624 | A | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.872+433A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801624 | |||||||
chr1:7801772 | G | A | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.872+581G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801772 | |||||||
chr1:7801832 | C | A | 1 | a0001c0019t0001g0300 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.872+641C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801832 | |||||||
chr1:7801894 | A | T | 3 | a0002c0002t0001g0213 a0002c0002t0001g0232 a0002c0002t0001g0233 |
3 | HG00408.hp1 HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.872+703A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801894 | |||||||
chr1:7801922 | G | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.872+731G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801922 | |||||||
chr1:7801980 | G | GTCAC | 5 | a0002c0002t0001g0230 a0002c0002t0001g0231 a0002c0002t0001g0262 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+790_872+791ins others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7801980 | ||||||
chr1:7802184 | C | A | 1 | a0002c0002t0001g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.873-863C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802184 | |||||||
chr1:7802261 | G | GT | 33 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0021t0005g0096 others(30): Show |
34 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.873-778dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7802261 | ||||||
chr1:7802261 | G | GTT | 6 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0067 others(3): Show |
6 | HG02257.hp2 HG02717.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.873-779_873-778dup others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7802261 | ||||||
chr1:7802306 | G | A | 2 | a0004c0006t0001g0030 a0004c0006t0001g0041 |
2 | HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.873-741G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802306 | |||||||
chr1:7802379 | C | T | 1 | a0001c0003t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.873-668C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802379 | |||||||
chr1:7802512 | G | A | 122 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(119): Show |
126 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.873-535G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802512 | |||||||
chr1:7802534 | G | T | 4 | a0001c0003t0001g0119 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | NA18948.hp1 NA18954.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-513G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802534 | |||||||
chr1:7802567 | G | A | 1 | a0011c0017t0017g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.873-480G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802567 | |||||||
chr1:7802632 | ACATCAT | A | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.873-412_873-407del others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7802632 | ||||||
chr1:7802764 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.873-283A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802764 | |||||||
chr1:7802839 | T | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.873-208T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802839 | |||||||
chr1:7802991 | A | T | 9 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(6): Show |
10 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-56A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802991 | |||||||
chr1:7802996 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.873-51A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802996 | |||||||
chr1:7803228 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0282 |
2 | NA18965.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.979+75T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803228 | |||||||
chr1:7803233 | C | T | 147 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0017 others(144): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.979+80C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803233 | |||||||
chr1:7803271 | T | C | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.979+118T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803271 | |||||||
chr1:7803359 | T | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+206T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803359 | |||||||
chr1:7803365 | A | G | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+212A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803365 | |||||||
chr1:7803367 | TTG | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+215_979+216del others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803367 | |||||||
chr1:7803371 | C | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+218C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803371 | |||||||
chr1:7803372 | T | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+219T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803372 | |||||||
chr1:7803384 | T | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+231T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803384 | |||||||
chr1:7803386 | G | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+233G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803386 | |||||||
chr1:7803394 | G | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+241G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803394 | |||||||
chr1:7803397 | T | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+244T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803397 | |||||||
chr1:7803401 | C | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+248C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803401 | |||||||
chr1:7803404 | C | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+251C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803404 | |||||||
chr1:7803406 | T | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+253T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803406 | |||||||
chr1:7803410 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.979+257G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803410 | |||||||
chr1:7803411 | T | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+258T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803411 | |||||||
chr1:7803413 | A | AC | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+263dupC | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803413 | ||||||
chr1:7803417 | A | G | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+264A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803417 | |||||||
chr1:7803421 | A | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+268A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803421 | |||||||
chr1:7803430 | G | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.980-262G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803430 | |||||||
chr1:7803433 | C | CAAAAAAT others(162): Show |
2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.980-254_980-253ins others(169): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(165): Show |
1 | a0002c0002t0001g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.980-254_980-253ins others(172): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(168): Show |
1 | a0002c0002t0012g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-254_980-253ins others(175): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(177): Show |
2 | a0002c0002t0001g0017 a0002c0002t0001g0191 |
3 | HG01168.hp1 HG01255.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.980-254_980-253ins others(184): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(178): Show |
4 | a0002c0002t0001g0189 a0002c0002t0001g0193 a0002c0002t0001g0195 others(1): Show |
4 | HG00733.hp1 HG02572.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-254_980-253ins others(185): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(179): Show |
2 | a0002c0002t0001g0192 a0002c0002t0001g0267 |
2 | HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.980-254_980-253ins others(186): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(181): Show |
3 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 |
3 | HG02145.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.980-254_980-253ins others(188): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(190): Show |
1 | a0002c0002t0001g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.980-254_980-253ins others(197): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803433 | C | CAAAAAAT others(194): Show |
1 | a0002c0002t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.980-254_980-253ins others(201): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | ||||||
chr1:7803570 | A | G | 1 | a0001c0009t0001g0323 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.980-122A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803570 | |||||||
chr1:7803675 | CTTA | C | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.980-11_980-9delATT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803675 | ||||||
chr1:7803880 | C | T | 1 | a0002c0002t0012g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1136+32C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7803880 | |||||||
chr1:7803884 | T | G | 8 | a0001c0004t0001g0023 a0001c0004t0001g0292 a0001c0004t0001g0293 others(5): Show |
9 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1136+36T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7803884 | |||||||
chr1:7803970 | G | A | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1136+122G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7803970 | |||||||
chr1:7804051 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1136+203A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804051 | |||||||
chr1:7804145 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1136+297T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804145 | |||||||
chr1:7804223 | A | G | 1 | a0004c0006t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1136+375A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804223 | |||||||
chr1:7804311 | C | CT | 38 | a0001c0001t0001g0274 a0001c0003t0001g0112 a0001c0003t0001g0113 others(35): Show |
41 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1136+478dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804311 | ||||||
chr1:7804311 | CT | C | 16 | a0001c0001t0001g0306 a0001c0001t0001g0335 a0001c0001t0001g0345 others(13): Show |
16 | HG00280.hp1 HG01975.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136+478delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804311 | ||||||
chr1:7804398 | C | CT | 33 | a0001c0003t0001g0122 a0001c0007t0001g0022 a0001c0007t0001g0250 others(30): Show |
36 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1136+565dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804398 | ||||||
chr1:7804497 | C | T | 1 | a0001c0003t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1136+649C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804497 | |||||||
chr1:7804608 | CCAGGCTG others(4): Show |
C | 1 | a0001c0004t0001g0166 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1136+763_1136+773d others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804608 | ||||||
chr1:7804694 | G | A | 1 | a0004c0006t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1136+846G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804694 | |||||||
chr1:7804813 | C | T | 1 | a0003c0005t0001g0079 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1136+965C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804813 | |||||||
chr1:7804873 | C | CT | 196 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(193): Show |
206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1136+1038dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804873 | ||||||
chr1:7804873 | C | CTT | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136+1037_1136+103 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804873 | ||||||
chr1:7804976 | C | A | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1136+1128C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804976 | |||||||
chr1:7805003 | G | A | 87 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(84): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+1155G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805003 | |||||||
chr1:7805018 | G | A | 4 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+1170G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805018 | |||||||
chr1:7805224 | C | T | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1136+1376C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805224 | |||||||
chr1:7805286 | GA | G | 1 | a0001c0001t0001g0007 | 3 | HG03041.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1136+1440delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7805286 | ||||||
chr1:7805407 | C | T | 87 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(84): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+1559C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805407 | |||||||
chr1:7805485 | G | A | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136+1637G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805485 | |||||||
chr1:7805573 | A | G | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1136+1725A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805573 | |||||||
chr1:7805618 | G | C | 2 | a0002c0002t0001g0017 a0002c0002t0001g0189 |
3 | HG00733.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1136+1770G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805618 | |||||||
chr1:7805631 | A | T | 87 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(84): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+1783A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805631 | |||||||
chr1:7805634 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1136+1786C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805634 | |||||||
chr1:7805650 | C | T | 25 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(22): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1136+1802C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805650 | |||||||
chr1:7805927 | A | G | 1 | a0001c0001t0001g0352 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1136+2079A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805927 | |||||||
chr1:7805977 | T | C | 1 | a0003c0005t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1136+2129T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805977 | |||||||
chr1:7806023 | G | A | 118 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0017 others(115): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1136+2175G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806023 | |||||||
chr1:7806080 | C | T | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1136+2232C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806080 | |||||||
chr1:7806196 | T | C | 1 | a0003c0005t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1136+2348T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806196 | |||||||
chr1:7806222 | C | T | 2 | a0003c0005t0001g0012 a0003c0005t0001g0158 |
3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1136+2374C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806222 | |||||||
chr1:7806350 | G | A | 29 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(26): Show |
31 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1136+2502G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806350 | |||||||
chr1:7806405 | A | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1137-2488A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806405 | |||||||
chr1:7806554 | G | A | 29 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(26): Show |
31 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1137-2339G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806554 | |||||||
chr1:7806646 | T | C | 1 | a0002c0020t0001g0355 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1137-2247T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806646 | |||||||
chr1:7806756 | T | A | 1 | a0002c0002t0001g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1137-2137T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806756 | |||||||
chr1:7806777 | G | C | 1 | a0004c0006t0001g0055 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1137-2116G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806777 | |||||||
chr1:7806795 | T | TA | 9 | a0001c0004t0002g0016 a0001c0004t0002g0170 a0001c0004t0002g0171 others(6): Show |
10 | HG00140.hp2 HG01074.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1137-2080dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806795 | ||||||
chr1:7806795 | T | TAAAAAAA others(4): Show |
1 | a0001c0003t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1137-2090_1137-208 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806795 | ||||||
chr1:7806795 | TAAA | T | 26 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0069 others(23): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1137-2082_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806795 | ||||||
chr1:7806801 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1137-2092A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806801 | |||||||
chr1:7806802 | A | ATATATAT others(8): Show |
1 | a0001c0007t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1137-2091_1137-209 others(19): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806802 | |||||||
chr1:7806804 | A | T | 2 | a0001c0007t0001g0261 a0002c0020t0001g0355 |
2 | NA18944.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1137-2089A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806804 | |||||||
chr1:7806806 | A | AATATATA others(1): Show |
5 | a0001c0001t0001g0340 a0002c0002t0001g0020 a0002c0002t0001g0202 others(2): Show |
6 | NA18953.hp2 NA18972.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137-2086_1137-208 others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | ||||||
chr1:7806806 | A | AATATATA others(5): Show |
5 | a0001c0001t0001g0255 a0001c0007t0001g0341 a0002c0002t0001g0227 others(2): Show |
5 | HG00544.hp2 NA18995.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-2086_1137-208 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | ||||||
chr1:7806806 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0348 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1137-2086_1137-208 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | ||||||
chr1:7806806 | A | AATATATA others(9): Show |
1 | a0002c0002t0001g0228 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1137-2086_1137-208 others(20): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | ||||||
chr1:7806806 | A | AATATATA others(15): Show |
2 | a0001c0001t0001g0342 a0001c0007t0001g0256 |
2 | HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1137-2086_1137-208 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | ||||||
chr1:7806806 | A | ATAT | 3 | a0002c0002t0001g0187 a0002c0002t0001g0231 a0002c0002t0001g0270 |
3 | HG02258.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1137-2087_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806806 | |||||||
chr1:7806806 | A | T | 8 | a0001c0001t0001g0359 a0001c0001t0001g0371 a0001c0007t0001g0261 others(5): Show |
8 | HG00673.hp2 HG02129.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-2087A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806806 | |||||||
chr1:7806807 | AAAAAAAT others(6): Show |
A | 1 | a0002c0002t0001g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1137-2084_1137-207 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806807 | ||||||
chr1:7806808 | A | AATAT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0283 others(14): Show |
18 | HG00733.hp2 HG01070.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | AATATAT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0181 others(7): Show |
11 | HG00741.hp2 HG01069.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | AATATATA others(3): Show |
6 | a0001c0001t0001g0273 a0001c0001t0001g0333 a0002c0002t0001g0002 others(3): Show |
6 | HG01109.hp2 HG01433.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | AATATATA others(5): Show |
2 | a0001c0001t0001g0282 a0001c0001t0001g0343 |
2 | HG04184.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0324 |
2 | HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0338 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1137-2084_1137-208 others(20): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | AATATATA others(11): Show |
1 | a0002c0013t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1137-2084_1137-208 others(22): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | ||||||
chr1:7806808 | A | ATATAT | 18 | a0001c0001t0001g0005 a0001c0001t0001g0303 a0001c0001t0001g0352 others(15): Show |
18 | HG00408.hp1 HG00621.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | |||||||
chr1:7806808 | A | ATATATAT | 7 | a0001c0001t0001g0309 a0001c0007t0001g0251 a0002c0002t0001g0184 others(4): Show |
7 | HG02027.hp2 HG02717.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | |||||||
chr1:7806808 | A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0299 a0002c0002t0001g0217 a0002c0002t0001g0260 |
3 | HG02738.hp2 NA18965.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | |||||||
chr1:7806808 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0008 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1137-2085_1137-208 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | |||||||
chr1:7806808 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0278 a0001c0001t0001g0339 |
2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(19): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | |||||||
chr1:7806808 | A | T | 33 | a0001c0001t0001g0255 a0001c0001t0001g0275 a0001c0001t0001g0286 others(30): Show |
34 | HG00280.hp2 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1137-2085A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | |||||||
chr1:7806810 | A | AATAT | 24 | a0001c0001t0001g0281 a0001c0001t0001g0284 a0001c0001t0001g0306 others(21): Show |
25 | HG00642.hp1 HG01069.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1137-2082_1137-208 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | AATATAT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0328 a0001c0004t0001g0168 others(2): Show |
6 | HG00099.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-2082_1137-208 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0280 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(22): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0289 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | AATATATA others(17): Show |
1 | a0001c0001t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | ||||||
chr1:7806810 | A | ATAT | 12 | a0001c0001t0001g0274 a0001c0001t0001g0304 a0001c0001t0001g0319 others(9): Show |
12 | HG00140.hp1 HG00423.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATAT | 29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0027 others(26): Show |
32 | HG00558.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT | 11 | a0001c0001t0001g0257 a0001c0001t0001g0331 a0001c0001t0001g0334 others(8): Show |
12 | HG00408.hp2 HG00735.hp2 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT others(2): Show |
9 | a0001c0001t0001g0007 a0001c0001t0001g0277 a0001c0001t0001g0291 others(6): Show |
9 | HG00438.hp2 HG01257.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT others(16): Show |
1 | a0002c0012t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0279 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806810 | A | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
127 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1137-2083A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | |||||||
chr1:7806811 | AAAT | A | 11 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(8): Show |
12 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806811 | ||||||
chr1:7806812 | A | AAAAAAAA others(10): Show |
1 | a0001c0003t0001g0011 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(21): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(16): Show |
1 | a0001c0003t0001g0135 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(22): Show |
1 | a0001c0003t0001g0122 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(15): Show |
2 | a0001c0003t0001g0123 a0001c0003t0001g0145 |
2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(17): Show |
1 | a0006c0010t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(19): Show |
2 | a0001c0003t0001g0147 a0001c0003t0001g0154 |
2 | NA18946.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(12): Show |
1 | a0001c0003t0001g0149 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(14): Show |
6 | a0001c0003t0001g0101 a0001c0003t0001g0115 a0001c0003t0001g0116 others(3): Show |
6 | HG01981.hp2 HG02135.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(16): Show |
4 | a0001c0003t0001g0011 a0001c0003t0001g0120 a0001c0003t0001g0129 others(1): Show |
4 | HG01074.hp2 HG02071.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(18): Show |
3 | a0001c0003t0001g0119 a0001c0003t0001g0143 a0001c0003t0001g0144 |
3 | NA18954.hp2 NA18978.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(22): Show |
1 | a0001c0003t0001g0146 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(13): Show |
4 | a0001c0003t0001g0113 a0001c0003t0001g0137 a0006c0010t0001g0130 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(24): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(15): Show |
3 | a0001c0003t0001g0118 a0001c0003t0001g0125 a0001c0003t0001g0151 |
3 | NA18986.hp2 NA18987.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(17): Show |
2 | a0001c0003t0001g0105 a0001c0027t0001g0131 |
2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0124 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(12): Show |
2 | a0001c0003t0001g0112 a0006c0010t0001g0127 |
2 | HG00741.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(14): Show |
10 | a0001c0003t0001g0068 a0001c0003t0001g0103 a0001c0003t0001g0136 others(7): Show |
10 | HG00621.hp1 HG01099.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(18): Show |
1 | a0001c0003t0001g0152 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(20): Show |
1 | a0001c0003t0001g0132 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(31): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(26): Show |
1 | a0001c0003t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(37): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(11): Show |
1 | a0001c0003t0001g0155 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(22): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(13): Show |
1 | a0001c0003t0001g0104 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(24): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(15): Show |
3 | a0001c0003t0001g0106 a0001c0003t0001g0117 a0001c0003t0001g0156 |
3 | HG00438.hp1 HG00673.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(12): Show |
2 | a0001c0003t0001g0108 a0001c0003t0001g0148 |
2 | HG01496.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(18): Show |
1 | a0001c0003t0001g0134 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(13): Show |
1 | a0001c0003t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(24): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(15): Show |
1 | a0001c0003t0001g0099 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(19): Show |
1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAAAAA others(16): Show |
1 | a0001c0003t0001g0157 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAAATAT others(4): Show |
1 | a0013c0026t0005g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAATATA others(3): Show |
2 | a0002c0013t0005g0097 a0002c0013t0005g0098 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AAAATATA others(7): Show |
2 | a0001c0001t0001g0008 a0002c0012t0001g0180 |
2 | HG02055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AATAT | 9 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0004t0001g0013 others(6): Show |
11 | HG01261.hp2 HG02155.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137-2060_1137-205 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AATATATA others(3): Show |
1 | a0001c0007t0001g0253 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1137-2066_1137-205 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1137-2078_1137-205 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | ||||||
chr1:7806812 | A | ATAT | 3 | a0001c0001t0001g0006 a0001c0001t0001g0349 a0001c0004t0002g0173 |
5 | HG02809.hp1 HG03130.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806812 | A | ATATAT | 15 | a0001c0001t0001g0004 a0001c0004t0001g0015 a0001c0004t0001g0293 others(12): Show |
15 | HG00280.hp1 HG01106.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806812 | A | ATATATAT | 7 | a0001c0001t0001g0325 a0001c0001t0013g0297 a0001c0007t0001g0205 others(4): Show |
7 | HG00639.hp1 HG02155.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806812 | A | ATATATAT others(2): Show |
3 | a0002c0002t0001g0018 a0002c0002t0001g0206 a0002c0002t0001g0242 |
3 | HG01261.hp1 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806812 | A | ATATATAT others(4): Show |
1 | a0002c0002t0001g0018 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1137-2081_1137-208 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806812 | A | ATATATAT others(6): Show |
1 | a0001c0009t0001g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1137-2081_1137-208 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806812 | A | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1137-2081A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | |||||||
chr1:7806813 | A | AAAAAAAA others(20): Show |
1 | a0001c0003t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(31): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806813 | |||||||
chr1:7806814 | T | A | 4 | a0001c0003t0001g0141 a0001c0004t0002g0172 a0008c0015t0001g0059 others(1): Show |
4 | HG01243.hp1 HG01891.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-2079T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806814 | |||||||
chr1:7806816 | T | A | 1 | a0001c0003t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-2077T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806816 | |||||||
chr1:7806818 | T | A | 1 | a0001c0003t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-2075T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806818 | |||||||
chr1:7806820 | T | A | 1 | a0001c0003t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-2073T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806820 | |||||||
chr1:7806836 | T | TA | 59 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(56): Show |
60 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1137-2057_1137-205 others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806836 | |||||||
chr1:7806837 | T | A | 2 | a0001c0003t0001g0100 a0001c0003t0001g0142 |
2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2056T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806837 | |||||||
chr1:7806838 | A | T | 2 | a0001c0003t0001g0100 a0001c0003t0001g0142 |
2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2055A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806838 | |||||||
chr1:7806839 | C | A | 2 | a0001c0003t0001g0100 a0001c0003t0001g0142 |
2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2054C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806839 | |||||||
chr1:7806839 | C | T | 59 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(56): Show |
60 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1137-2054C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806839 | |||||||
chr1:7806840 | A | AT | 59 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(56): Show |
60 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1137-2052dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806840 | ||||||
chr1:7806840 | A | G | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1137-2053A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806840 | |||||||
chr1:7806840 | A | T | 2 | a0001c0003t0001g0100 a0001c0003t0001g0142 |
2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2053A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806840 | |||||||
chr1:7806841 | T | TAC | 5 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(2): Show |
5 | HG00735.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-2040_1137-203 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806841 | ||||||
chr1:7806855 | T | C | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1137-2038T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806855 | |||||||
chr1:7807084 | C | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-1809C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807084 | |||||||
chr1:7807195 | G | A | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1137-1698G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807195 | |||||||
chr1:7807256 | T | C | 1 | a0002c0012t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-1637T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807256 | |||||||
chr1:7807285 | T | C | 1 | a0002c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1137-1608T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807285 | |||||||
chr1:7807325 | G | A | 2 | a0001c0004t0002g0016 a0001c0004t0002g0174 |
3 | HG02258.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1137-1568G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807325 | |||||||
chr1:7807394 | T | C | 3 | a0002c0013t0005g0097 a0002c0013t0005g0098 a0013c0026t0005g0095 |
3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1137-1499T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807394 | |||||||
chr1:7807686 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1137-1207G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807686 | |||||||
chr1:7808061 | C | T | 4 | a0004c0006t0001g0033 a0004c0006t0001g0034 a0004c0006t0001g0035 others(1): Show |
4 | HG01109.hp2 HG01433.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-832C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808061 | |||||||
chr1:7808116 | C | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-777C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808116 | |||||||
chr1:7808160 | G | A | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1137-733G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808160 | |||||||
chr1:7808232 | C | CA | 69 | a0001c0003t0001g0152 a0001c0004t0011g0064 a0002c0002t0001g0002 others(66): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1137-634dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | C | CAA | 63 | a0001c0003t0001g0068 a0001c0003t0001g0100 a0001c0003t0001g0101 others(60): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1137-635_1137-634d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | C | CAAA | 21 | a0001c0003t0001g0011 a0001c0003t0001g0099 a0001c0003t0001g0104 others(18): Show |
22 | HG00735.hp1 HG01192.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1137-636_1137-634d others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | C | CAAAA | 12 | a0001c0003t0001g0116 a0001c0003t0001g0149 a0003c0005t0001g0010 others(9): Show |
13 | HG00738.hp1 HG01123.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1137-637_1137-634d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | C | CAAAAA | 12 | a0003c0005t0001g0070 a0003c0005t0001g0071 a0003c0005t0001g0072 others(9): Show |
12 | HG01106.hp2 HG01175.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-638_1137-634d others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | C | CAAAAAA | 5 | a0003c0005t0001g0012 a0003c0005t0001g0069 a0003c0005t0001g0083 others(2): Show |
6 | HG02895.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-639_1137-634d others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0001g0337 |
3 | NA18979.hp1 NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1137-644_1137-634d others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808232 | CAAAAAAA others(5): Show |
C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1137-645_1137-634d others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | ||||||
chr1:7808268 | G | C | 4 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0324 others(1): Show |
4 | HG00733.hp2 HG02293.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-625G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808268 | |||||||
chr1:7808290 | G | A | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1137-603G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808290 | |||||||
chr1:7808308 | G | C | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1137-585G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808308 | |||||||
chr1:7808357 | T | C | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1137-536T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808357 | |||||||
chr1:7808376 | G | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-517G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808376 | |||||||
chr1:7808665 | T | C | 130 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(127): Show |
134 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.1137-228T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808665 | |||||||
chr1:7808844 | C | T | 1 | a0002c0012t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-49C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808844 | |||||||
chr1:7809320 | A | G | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1242+322A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809320 | |||||||
chr1:7809321 | G | A | 3 | a0001c0003t0001g0123 a0001c0003t0001g0126 a0001c0003t0001g0145 |
3 | HG02027.hp1 NA18968.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1242+323G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809321 | |||||||
chr1:7809425 | T | G | 1 | a0002c0002t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1242+427T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809425 | |||||||
chr1:7809437 | G | A | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1242+439G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809437 | |||||||
chr1:7809533 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1243-360C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809533 | |||||||
chr1:7809673 | C | T | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1243-220C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809673 | |||||||
chr1:7809687 | A | T | 28 | a0001c0003t0001g0101 a0001c0003t0001g0103 a0001c0003t0001g0104 others(25): Show |
28 | HG00438.hp1 HG00621.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1243-206A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809687 | |||||||
chr1:7809729 | G | C | 3 | a0001c0001t0001g0357 a0001c0011t0001g0025 a0001c0011t0001g0330 |
4 | NA19011.hp1 NA19074.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243-164G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809729 | |||||||
chr1:7809855 | G | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1243-38G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809855 | |||||||
chr1:7810084 | A | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1371+63A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810084 | |||||||
chr1:7810141 | A | G | 1 | a0003c0005t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1371+120A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810141 | |||||||
chr1:7810276 | C | A | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372-162C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810276 | |||||||
chr1:7810358 | C | T | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1372-80C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810358 | |||||||
chr1:7810655 | A | C | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1522+67A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7810655 | |||||||
chr1:7811144 | T | C | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+556T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811144 | |||||||
chr1:7811169 | T | C | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1522+581T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811169 | |||||||
chr1:7811190 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0321 a0001c0001t0009g0322 others(1): Show |
4 | HG00423.hp1 NA18961.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1522+602C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811190 | |||||||
chr1:7811289 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+701A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811289 | |||||||
chr1:7811327 | A | G | 1 | a0001c0001t0001g0006 | 3 | HG02809.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1522+739A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811327 | |||||||
chr1:7811370 | A | G | 1 | a0002c0002t0001g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1522+782A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811370 | |||||||
chr1:7811421 | AG | A | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+834delG | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811421 | |||||||
chr1:7811524 | C | T | 26 | a0001c0003t0001g0101 a0001c0003t0001g0103 a0001c0003t0001g0104 others(23): Show |
26 | HG00438.hp1 HG00621.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.1522+936C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811524 | |||||||
chr1:7811748 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1522+1160A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811748 | |||||||
chr1:7811789 | C | T | 9 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(6): Show |
10 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522+1201C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811789 | |||||||
chr1:7812016 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+1428A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812016 | |||||||
chr1:7812128 | C | T | 1 | a0001c0001t0001g0350 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1522+1540C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812128 | |||||||
chr1:7812267 | A | AT | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1522+1688dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812267 | ||||||
chr1:7812393 | G | A | 73 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(70): Show |
76 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1522+1805G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812393 | |||||||
chr1:7812422 | C | G | 24 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(21): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.1522+1834C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812422 | |||||||
chr1:7812423 | G | A | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1522+1835G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812423 | |||||||
chr1:7812493 | T | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1522+1905T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812493 | |||||||
chr1:7812500 | C | T | 1 | a0002c0012t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1522+1912C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812500 | |||||||
chr1:7812540 | G | A | 13 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(10): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1522+1952G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812540 | |||||||
chr1:7812550 | G | A | 2 | a0002c0002t0001g0264 a0002c0002t0001g0265 |
2 | NA18957.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1522+1962G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812550 | |||||||
chr1:7812582 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0255 a0001c0001t0001g0338 others(5): Show |
10 | HG02056.hp1 HG03834.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1522+1994G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812582 | |||||||
chr1:7812608 | G | C | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+2020G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812608 | |||||||
chr1:7812624 | C | CA | 9 | a0001c0001t0001g0321 a0001c0001t0001g0331 a0001c0001t0001g0342 others(6): Show |
9 | HG02056.hp1 HG04184.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.1522+2061dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAA | 52 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(49): Show |
54 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1522+2059_1522+206 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAAA | 10 | a0001c0003t0001g0103 a0001c0003t0001g0106 a0001c0003t0001g0116 others(7): Show |
10 | HG00438.hp1 HG01975.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1522+2058_1522+206 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAAAA | 50 | a0001c0003t0001g0145 a0001c0004t0011g0064 a0002c0002t0001g0197 others(47): Show |
52 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1522+2057_1522+206 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAAAAA | 18 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0192 others(15): Show |
19 | HG00733.hp1 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1522+2056_1522+206 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAAAAAA | 9 | a0002c0002t0001g0191 a0002c0002t0001g0194 a0002c0002t0001g0195 others(6): Show |
9 | HG01243.hp1 HG01358.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1522+2055_1522+206 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAAAAAA others(3): Show |
7 | a0002c0002t0001g0067 a0002c0002t0001g0184 a0002c0002t0001g0187 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522+2052_1522+206 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | C | CAAAAAAA others(4): Show |
7 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0185 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522+2051_1522+206 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | CA | C | 28 | a0001c0001t0001g0274 a0001c0001t0001g0284 a0001c0001t0001g0287 others(25): Show |
35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.1522+2061delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | CAA | C | 7 | a0001c0004t0001g0161 a0002c0002t0001g0183 a0002c0002t0001g0266 others(4): Show |
7 | HG02055.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1522+2060_1522+206 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812624 | CAAAAAA | C | 47 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(44): Show |
53 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1522+2056_1522+206 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | ||||||
chr1:7812742 | T | C | 1 | a0001c0004t0001g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1522+2154T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812742 | |||||||
chr1:7812764 | T | C | 1 | a0005c0008t0003g0368 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1522+2176T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812764 | |||||||
chr1:7812775 | G | T | 1 | a0003c0005t0010g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1522+2187G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812775 | |||||||
chr1:7812796 | A | T | 1 | a0008c0015t0001g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1522+2208A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812796 | |||||||
chr1:7812823 | G | A | 1 | a0005c0024t0014g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1522+2235G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812823 | |||||||
chr1:7812887 | T | G | 1 | a0004c0006t0001g0029 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1522+2299T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812887 | |||||||
chr1:7813015 | T | C | 27 | a0003c0005t0001g0010 a0003c0005t0001g0069 a0003c0005t0001g0070 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1522+2427T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813015 | |||||||
chr1:7813443 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1522+2855A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813443 | |||||||
chr1:7813491 | C | T | 1 | a0002c0013t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1522+2903C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813491 | |||||||
chr1:7813533 | G | A | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1522+2945G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813533 | |||||||
chr1:7813741 | G | A | 3 | a0002c0002t0001g0210 a0002c0002t0001g0216 a0002c0002t0001g0229 |
3 | HG00280.hp2 HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1522+3153G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813741 | |||||||
chr1:7813795 | T | A | 66 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(63): Show |
67 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1522+3207T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813795 | |||||||
chr1:7813979 | C | A | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+3391C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813979 | |||||||
chr1:7813982 | C | G | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+3394C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813982 | |||||||
chr1:7813983 | G | A | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1522+3395G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813983 | |||||||
chr1:7814002 | A | G | 1 | a0001c0003t0001g0132 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1522+3414A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814002 | |||||||
chr1:7814186 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0295 others(17): Show |
23 | HG00423.hp1 HG00558.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.1522+3598G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814186 | |||||||
chr1:7814731 | C | A | 6 | a0004c0006t0001g0031 a0004c0006t0001g0032 a0004c0006t0001g0033 others(3): Show |
6 | HG01109.hp2 HG01433.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1522+4143C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814731 | |||||||
chr1:7814915 | C | T | 32 | a0001c0021t0005g0096 a0002c0002t0001g0241 a0004c0006t0001g0009 others(29): Show |
33 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1522+4327C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814915 | |||||||
chr1:7815015 | A | G | 1 | a0002c0002t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1523-4270A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815015 | |||||||
chr1:7815182 | T | C | 1 | a0002c0002t0001g0217 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1523-4103T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815182 | |||||||
chr1:7815411 | C | T | 2 | a0003c0005t0001g0012 a0003c0005t0001g0158 |
3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1523-3874C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815411 | |||||||
chr1:7815550 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1523-3735A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815550 | |||||||
chr1:7815723 | C | T | 1 | a0002c0002t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1523-3562C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815723 | |||||||
chr1:7815752 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
118 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1523-3533G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815752 | |||||||
chr1:7815829 | C | CA | 15 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0333 others(12): Show |
18 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1523-3442dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815829 | ||||||
chr1:7815829 | CA | C | 14 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(11): Show |
15 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1523-3442delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815829 | ||||||
chr1:7815986 | C | T | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1523-3299C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815986 | |||||||
chr1:7815987 | G | A | 1 | a0001c0001t0001g0007 | 3 | HG03041.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1523-3298G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815987 | |||||||
chr1:7815991 | C | CA | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1523-3268dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAA | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1523-3269_1523-326 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAA | 18 | a0001c0001t0001g0027 a0001c0001t0001g0298 a0001c0001t0001g0309 others(15): Show |
19 | HG01106.hp2 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1523-3270_1523-326 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(4): Show |
1 | a0001c0003t0001g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1523-3278_1523-326 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(5): Show |
3 | a0001c0003t0001g0011 a0001c0003t0001g0116 a0001c0003t0001g0149 |
4 | NA18956.hp2 NA18957.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523-3279_1523-326 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(8): Show |
1 | a0001c0003t0001g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1523-3282_1523-326 others(19): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(14): Show |
1 | a0006c0010t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1523-3288_1523-326 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(15): Show |
12 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0129 others(9): Show |
12 | HG01074.hp2 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523-3289_1523-326 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(16): Show |
16 | a0001c0003t0001g0101 a0001c0003t0001g0104 a0001c0003t0001g0105 others(13): Show |
16 | HG00438.hp1 HG00673.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1523-3290_1523-326 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(17): Show |
6 | a0001c0003t0001g0108 a0001c0003t0001g0119 a0001c0003t0001g0141 others(3): Show |
6 | HG00621.hp1 HG02004.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1523-3291_1523-326 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(19): Show |
1 | a0001c0003t0001g0148 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1523-3293_1523-326 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(20): Show |
1 | a0001c0003t0001g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(31): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(21): Show |
2 | a0001c0003t0001g0142 a0001c0003t0004g0107 |
2 | HG02135.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1523-3268_1523-326 others(32): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(22): Show |
2 | a0001c0003t0001g0099 a0001c0003t0001g0136 |
2 | HG01099.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1523-3268_1523-326 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(25): Show |
1 | a0001c0003t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(36): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(26): Show |
1 | a0001c0003t0001g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(37): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(27): Show |
1 | a0001c0003t0001g0132 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(38): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(31): Show |
1 | a0001c0003t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(42): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | C | CAAAAAAA others(18): Show |
1 | a0001c0003t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1523-3276_1523-327 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | CA | C | 61 | a0001c0028t0001g0347 a0002c0002t0001g0002 a0002c0002t0001g0018 others(58): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1523-3268delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7815991 | CAAAAAAA | C | 32 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0004c0006t0001g0009 others(29): Show |
34 | HG00642.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1523-3274_1523-326 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | ||||||
chr1:7816015 | A | AAAAAAAA others(12): Show |
1 | a0002c0013t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816015 | ||||||
chr1:7816015 | A | AAAAAAAA others(6): Show |
1 | a0013c0026t0005g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816015 | ||||||
chr1:7816015 | A | AAAAAAAA others(5): Show |
2 | a0002c0013t0005g0097 a0002c0013t0005g0098 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1523-3268_1523-326 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816015 | ||||||
chr1:7816106 | T | C | 149 | a0001c0021t0005g0096 a0001c0028t0001g0347 a0002c0002t0001g0002 others(146): Show |
159 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1523-3179T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816106 | |||||||
chr1:7816116 | AAAG | A | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523-3163_1523-316 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816116 | ||||||
chr1:7816186 | T | A | 214 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(211): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1523-3099T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816186 | |||||||
chr1:7816189 | A | G | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1523-3096A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816189 | |||||||
chr1:7816278 | TAA | T | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1523-3006_1523-300 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816278 | |||||||
chr1:7816332 | T | C | 5 | a0001c0001t0001g0285 a0001c0003t0001g0119 a0001c0003t0001g0143 others(2): Show |
5 | HG03471.hp2 NA18948.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523-2953T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816332 | |||||||
chr1:7816364 | A | G | 1 | a0001c0003t0001g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1523-2921A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816364 | |||||||
chr1:7816416 | G | A | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1523-2869G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816416 | |||||||
chr1:7816463 | T | C | 12 | a0001c0007t0001g0021 a0001c0007t0001g0022 a0001c0007t0001g0205 others(9): Show |
14 | HG00423.hp2 HG02056.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1523-2822T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816463 | |||||||
chr1:7816530 | A | G | 1 | a0001c0001t0001g0006 | 3 | HG02809.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1523-2755A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816530 | |||||||
chr1:7816628 | A | G | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2657A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816628 | |||||||
chr1:7816629 | C | CCA | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2656_1523-265 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816629 | |||||||
chr1:7816630 | A | T | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2655A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816630 | |||||||
chr1:7816631 | C | T | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2654C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816631 | |||||||
chr1:7816633 | A | T | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2652A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816633 | |||||||
chr1:7816638 | T | G | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2647T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816638 | |||||||
chr1:7816639 | C | A | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2646C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816639 | |||||||
chr1:7816644 | A | T | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2641A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816644 | |||||||
chr1:7816645 | GAA | G | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2639_1523-263 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816645 | |||||||
chr1:7816648 | T | G | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2637T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816648 | |||||||
chr1:7816649 | G | T | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2636G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816649 | |||||||
chr1:7816651 | C | T | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2634C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816651 | |||||||
chr1:7816663 | A | T | 1 | a0004c0006t0001g0032 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1523-2622A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816663 | |||||||
chr1:7816946 | G | A | 1 | a0001c0003t0001g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1523-2339G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816946 | |||||||
chr1:7816948 | G | A | 210 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(207): Show |
221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1523-2337G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816948 | |||||||
chr1:7817343 | C | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0212 |
2 | HG01123.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1523-1942C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817343 | |||||||
chr1:7817428 | A | G | 217 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(214): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-1857A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817428 | |||||||
chr1:7817490 | T | C | 5 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0198 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523-1795T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817490 | |||||||
chr1:7817706 | G | A | 5 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523-1579G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817706 | |||||||
chr1:7817718 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1523-1567G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817718 | |||||||
chr1:7817727 | T | C | 1 | a0001c0003t0001g0126 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1523-1558T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817727 | |||||||
chr1:7817740 | A | T | 3 | a0002c0013t0005g0097 a0002c0013t0005g0098 a0013c0026t0005g0095 |
3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1523-1545A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817740 | |||||||
chr1:7817846 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1523-1439C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817846 | |||||||
chr1:7817874 | T | C | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1523-1411T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817874 | |||||||
chr1:7817887 | A | G | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1523-1398A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817887 | |||||||
chr1:7817996 | A | G | 217 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(214): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-1289A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817996 | |||||||
chr1:7818480 | C | A | 1 | a0002c0002t0012g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1523-805C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818480 | |||||||
chr1:7818487 | A | G | 217 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(214): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-798A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818487 | |||||||
chr1:7818508 | C | T | 8 | a0001c0004t0001g0015 a0001c0004t0001g0162 a0001c0004t0001g0165 others(5): Show |
9 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1523-777C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818508 | |||||||
chr1:7818574 | A | G | 11 | a0002c0002t0001g0018 a0002c0002t0001g0203 a0002c0002t0001g0206 others(8): Show |
12 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523-711A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818574 | |||||||
chr1:7818661 | G | A | 1 | a0001c0003t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1523-624G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818661 | |||||||
chr1:7818902 | C | T | 2 | a0001c0003t0001g0108 a0001c0003t0001g0155 |
2 | NA18959.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1523-383C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818902 | |||||||
chr1:7818905 | A | G | 1 | a0001c0003t0001g0155 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1523-380A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818905 | |||||||
chr1:7819003 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1523-282C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819003 | |||||||
chr1:7819059 | C | G | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1523-226C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819059 | |||||||
chr1:7819070 | T | G | 217 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(214): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-215T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819070 | |||||||
chr1:7819108 | G | A | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1523-177G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819108 | |||||||
chr1:7819141 | G | C | 2 | a0001c0004t0001g0165 a0001c0004t0001g0168 |
2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1523-144G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819141 | |||||||
chr1:7819156 | T | C | 3 | a0001c0001t0001g0327 a0001c0001t0001g0329 a0001c0001t0001g0353 |
3 | HG01884.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1523-129T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819156 | |||||||
chr1:7819262 | C | T | 24 | a0004c0006t0001g0009 a0004c0006t0001g0029 a0004c0006t0001g0030 others(21): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1523-23C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819262 | |||||||
chr1:7819422 | T | C | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | splice_donor_variant&intron_variant | HIGH | c.1658+2T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819422 | |||||||
chr1:7819444 | C | A | 1 | a0004c0006t0001g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1658+24C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819444 | |||||||
chr1:7819461 | G | A | 1 | a0001c0004t0002g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1658+41G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819461 | |||||||
chr1:7819567 | C | T | 26 | a0001c0003t0001g0135 a0001c0004t0001g0013 a0001c0004t0001g0014 others(23): Show |
33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1658+147C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819567 | |||||||
chr1:7819625 | T | C | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1658+205T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819625 | |||||||
chr1:7819792 | A | AT | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
270 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.1659-308dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 7819792 | ||||||
chr1:7819879 | G | A | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1659-236G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819879 | |||||||
chr1:7820312 | T | C | 11 | a0001c0004t0002g0001 a0001c0004t0002g0016 a0001c0004t0002g0164 others(8): Show |
15 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783+73T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820312 | |||||||
chr1:7820321 | A | G | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1783+82A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820321 | |||||||
chr1:7820365 | A | G | 1 | a0011c0017t0017g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1784-102A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820365 | |||||||
chr1:7820409 | A | G | 217 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(214): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1784-58A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820409 | |||||||
chr1:7820419 | C | G | 7 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1784-48C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820419 | |||||||
chr1:7820422 | G | A | 5 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-45G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820422 | |||||||
chr1:7820652 | G | A | 2 | a0004c0006t0001g0030 a0004c0006t0001g0041 |
2 | HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1957+12G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820652 | |||||||
chr1:7820698 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1957+58G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820698 | |||||||
chr1:7820727 | C | G | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1957+87C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820727 | |||||||
chr1:7820787 | T | G | 1 | a0003c0005t0001g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1957+147T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820787 | |||||||
chr1:7820845 | T | C | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1957+205T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820845 | |||||||
chr1:7820958 | T | C | 4 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+318T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820958 | |||||||
chr1:7820994 | G | A | 4 | a0004c0006t0001g0033 a0004c0006t0001g0034 a0004c0006t0001g0035 others(1): Show |
4 | HG01109.hp2 HG01433.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+354G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820994 | |||||||
chr1:7821154 | C | T | 1 | a0002c0002t0001g0222 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1957+514C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821154 | |||||||
chr1:7821174 | C | T | 25 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(22): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957+534C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821174 | |||||||
chr1:7821190 | C | T | 4 | a0001c0004t0002g0001 a0001c0004t0002g0164 a0001c0004t0002g0169 others(1): Show |
7 | HG00639.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957+550C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821190 | |||||||
chr1:7821210 | G | A | 1 | a0002c0002t0012g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1957+570G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821210 | |||||||
chr1:7821255 | T | A | 1 | a0001c0003t0001g0155 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1957+615T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821255 | |||||||
chr1:7821618 | C | T | 1 | a0002c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1957+978C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821618 | |||||||
chr1:7821672 | G | A | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1957+1032G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821672 | |||||||
chr1:7821708 | A | T | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1957+1068A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821708 | |||||||
chr1:7821720 | C | T | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1957+1080C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821720 | |||||||
chr1:7821859 | T | C | 1 | a0002c0012t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1957+1219T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821859 | |||||||
chr1:7821943 | G | C | 1 | a0001c0001t0001g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1957+1303G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821943 | |||||||
chr1:7822250 | A | T | 1 | a0002c0002t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1957+1610A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822250 | |||||||
chr1:7822258 | AT | A | 211 | a0001c0001t0001g0309 a0001c0003t0001g0011 a0001c0003t0001g0068 others(208): Show |
222 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1957+1633delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7822258 | ||||||
chr1:7822260 | T | A | 1 | a0003c0005t0001g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1957+1620T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822260 | |||||||
chr1:7822319 | G | A | 1 | a0001c0003t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1957+1679G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822319 | |||||||
chr1:7822395 | A | G | 217 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(214): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1957+1755A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822395 | |||||||
chr1:7822479 | C | T | 5 | a0002c0002t0001g0230 a0002c0002t0001g0231 a0002c0002t0001g0262 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1957+1839C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822479 | |||||||
chr1:7822490 | T | A | 1 | a0001c0003t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1957+1850T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822490 | |||||||
chr1:7822496 | G | T | 3 | a0002c0013t0005g0097 a0002c0013t0005g0098 a0013c0026t0005g0095 |
3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1957+1856G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822496 | |||||||
chr1:7822976 | T | C | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1957+2336T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822976 | |||||||
chr1:7822999 | T | G | 2 | a0004c0006t0001g0039 a0004c0006t0001g0048 |
2 | HG00741.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1957+2359T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822999 | |||||||
chr1:7823127 | C | G | 1 | a0001c0001t0001g0371 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1957+2487C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823127 | |||||||
chr1:7823132 | C | T | 4 | a0001c0003t0001g0124 a0001c0003t0001g0128 a0001c0003t0001g0132 others(1): Show |
4 | HG01934.hp2 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+2492C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823132 | |||||||
chr1:7823298 | A | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1957+2658A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823298 | |||||||
chr1:7823364 | C | T | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1957+2724C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823364 | |||||||
chr1:7823400 | T | C | 78 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(75): Show |
85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1957+2760T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823400 | |||||||
chr1:7823500 | G | C | 1 | a0001c0001t0001g0346 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1957+2860G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823500 | |||||||
chr1:7823557 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1957+2917G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823557 | |||||||
chr1:7823598 | C | T | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1958-2882C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823598 | |||||||
chr1:7823746 | T | G | 1 | a0004c0006t0001g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1958-2734T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823746 | |||||||
chr1:7823769 | G | A | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1958-2711G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823769 | |||||||
chr1:7823774 | A | G | 214 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(211): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1958-2706A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823774 | |||||||
chr1:7824110 | A | G | 1 | a0001c0004t0001g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1958-2370A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824110 | |||||||
chr1:7824112 | G | A | 1 | a0001c0001t0001g0357 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1958-2368G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824112 | |||||||
chr1:7824165 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1958-2315G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824165 | |||||||
chr1:7824343 | T | G | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1958-2137T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824343 | |||||||
chr1:7824370 | C | T | 1 | a0002c0002t0001g0220 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1958-2110C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824370 | |||||||
chr1:7824465 | G | T | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1958-2015G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824465 | |||||||
chr1:7824509 | C | T | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1958-1971C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824509 | |||||||
chr1:7824520 | T | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1958-1960T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824520 | |||||||
chr1:7824573 | T | C | 7 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1958-1907T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824573 | |||||||
chr1:7824632 | T | C | 6 | a0002c0002t0001g0230 a0002c0002t0001g0231 a0002c0002t0001g0241 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-1848T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824632 | |||||||
chr1:7824949 | G | A | 3 | a0001c0003t0001g0112 a0001c0003t0001g0113 a0001c0003t0001g0115 |
3 | NA18963.hp1 NA18966.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1958-1531G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824949 | |||||||
chr1:7825042 | C | CT | 6 | a0001c0004t0006g0159 a0001c0004t0006g0160 a0001c0004t0006g0163 others(3): Show |
6 | HG00280.hp1 HG01261.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1958-1426dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7825042 | ||||||
chr1:7825294 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1958-1186A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825294 | |||||||
chr1:7825296 | A | T | 1 | a0001c0021t0005g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1958-1184A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825296 | |||||||
chr1:7825424 | A | G | 3 | a0002c0002t0001g0230 a0002c0002t0001g0231 a0002c0002t0001g0270 |
3 | HG02280.hp1 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1958-1056A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825424 | |||||||
chr1:7825848 | G | A | 2 | a0003c0005t0001g0012 a0003c0005t0001g0158 |
3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1958-632G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825848 | |||||||
chr1:7825891 | C | CAA | 203 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(200): Show |
213 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1958-576_1958-575d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7825891 | ||||||
chr1:7825891 | C | CAAA | 11 | a0001c0003t0001g0101 a0001c0003t0001g0136 a0001c0003t0001g0137 others(8): Show |
12 | HG01099.hp2 HG01123.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1958-577_1958-575d others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7825891 | ||||||
chr1:7825916 | C | A | 1 | a0002c0002t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1958-564C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825916 | |||||||
chr1:7826024 | G | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1958-456G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826024 | |||||||
chr1:7826056 | G | C | 69 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(66): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1958-424G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826056 | |||||||
chr1:7826057 | C | T | 69 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(66): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1958-423C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826057 | |||||||
chr1:7826097 | G | C | 1 | a0002c0002t0001g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1958-383G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826097 | |||||||
chr1:7826281 | T | A | 1 | a0003c0005t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1958-199T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826281 | |||||||
chr1:7826364 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1958-116G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826364 | |||||||
chr1:7826429 | A | G | 1 | a0001c0003t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1958-51A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826429 | |||||||
chr1:7826746 | A | G | 5 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2188+36A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7826746 | |||||||
chr1:7826857 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
6 | HG02809.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2188+147A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7826857 | |||||||
chr1:7826963 | G | A | 1 | a0001c0021t0005g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2189-155G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7826963 | |||||||
chr1:7827043 | C | G | 1 | a0002c0002t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2189-75C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7827043 | |||||||
chr1:7827866 | A | G | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2886+51A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7827866 | |||||||
chr1:7827949 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0255 a0001c0001t0001g0338 others(5): Show |
10 | HG02056.hp1 HG03834.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.2886+134C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7827949 | |||||||
chr1:7828098 | T | C | 365 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(362): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.2886+283T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828098 | |||||||
chr1:7828109 | A | C | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.2886+294A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828109 | |||||||
chr1:7828155 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2886+340A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828155 | |||||||
chr1:7828168 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2886+353C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828168 | |||||||
chr1:7828228 | C | T | 2 | a0001c0004t0002g0016 a0001c0004t0002g0174 |
3 | HG02258.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2886+413C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828228 | |||||||
chr1:7828378 | C | T | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.2886+563C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828378 | |||||||
chr1:7828512 | T | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.2886+697T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828512 | |||||||
chr1:7828670 | G | C | 24 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(21): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2886+855G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828670 | |||||||
chr1:7829092 | C | T | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.2887-742C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829092 | |||||||
chr1:7829214 | A | G | 1 | a0001c0003t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2887-620A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829214 | |||||||
chr1:7829214 | A | T | 13 | a0001c0001t0001g0257 a0001c0007t0001g0021 a0001c0007t0001g0022 others(10): Show |
15 | HG00423.hp2 HG02056.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.2887-620A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829214 | |||||||
chr1:7829225 | A | G | 1 | a0004c0006t0001g0029 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2887-609A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829225 | |||||||
chr1:7829318 | A | C | 365 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(362): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.2887-516A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829318 | |||||||
chr1:7829487 | G | T | 1 | a0002c0002t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2887-347G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829487 | |||||||
chr1:7829744 | C | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
300 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2887-90C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829744 | |||||||
chr1:7829781 | G | C | 3 | a0002c0002t0001g0213 a0002c0002t0001g0232 a0002c0002t0001g0233 |
3 | HG00408.hp1 HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.2887-53G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829781 | |||||||
chr1:7830204 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
300 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.3214+43A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830204 | |||||||
chr1:7830585 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3214+424A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830585 | |||||||
chr1:7830741 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.3214+580C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830741 | |||||||
chr1:7830787 | C | T | 1 | a0003c0005t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3214+626C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830787 | |||||||
chr1:7830896 | G | C | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
307 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3214+735G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830896 | |||||||
chr1:7831023 | A | T | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3214+862A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831023 | |||||||
chr1:7831037 | A | C | 12 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(9): Show |
12 | HG00438.hp2 HG00558.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.3214+876A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831037 | |||||||
chr1:7831318 | C | T | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3214+1157C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831318 | |||||||
chr1:7831409 | CT | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0314 a0001c0001t0001g0319 |
3 | HG00642.hp1 HG01515.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3214+1250delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7831409 | ||||||
chr1:7831563 | C | A | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+1402C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831563 | |||||||
chr1:7831574 | A | G | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3214+1413A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831574 | |||||||
chr1:7831737 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.3214+1576C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831737 | |||||||
chr1:7831789 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3214+1628A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831789 | |||||||
chr1:7832049 | T | A | 61 | a0001c0021t0005g0096 a0003c0005t0001g0010 a0003c0005t0001g0012 others(58): Show |
64 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.3214+1888T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832049 | |||||||
chr1:7832366 | CT | C | 96 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0278 others(93): Show |
100 | HG00558.hp2 HG00642.hp2 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.3214+2226delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832366 | ||||||
chr1:7832366 | CTT | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
194 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.3214+2225_3214+222 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832366 | ||||||
chr1:7832366 | CTTT | C | 25 | a0001c0001t0001g0280 a0001c0004t0001g0013 a0001c0004t0001g0014 others(22): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3214+2224_3214+222 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832366 | ||||||
chr1:7832393 | G | A | 366 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(363): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.3214+2232G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832393 | |||||||
chr1:7832499 | G | A | 87 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(84): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3214+2338G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832499 | |||||||
chr1:7832563 | C | T | 82 | a0001c0021t0005g0096 a0002c0002t0001g0002 a0002c0002t0001g0018 others(79): Show |
89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.3214+2402C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832563 | |||||||
chr1:7832619 | C | T | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3214+2458C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832619 | |||||||
chr1:7832718 | AT | A | 305 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.3214+2567delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832718 | ||||||
chr1:7832786 | C | T | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3214+2625C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832786 | |||||||
chr1:7832811 | A | G | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3214+2650A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832811 | |||||||
chr1:7832815 | C | G | 2 | a0001c0004t0002g0016 a0001c0004t0002g0174 |
3 | HG02258.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3214+2654C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832815 | |||||||
chr1:7832837 | A | AT | 11 | a0001c0001t0001g0298 a0001c0001t0001g0339 a0001c0004t0002g0164 others(8): Show |
11 | HG00639.hp2 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.3214+2694dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832837 | ||||||
chr1:7832837 | AT | A | 9 | a0001c0001t0001g0303 a0001c0003t0001g0100 a0001c0003t0001g0116 others(6): Show |
9 | HG01069.hp1 HG01261.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3214+2694delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832837 | ||||||
chr1:7832856 | G | T | 51 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(48): Show |
57 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.3214+2695G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832856 | |||||||
chr1:7832863 | A | G | 1 | a0001c0021t0005g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3214+2702A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832863 | |||||||
chr1:7832870 | A | G | 1 | a0003c0005t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3214+2709A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832870 | |||||||
chr1:7833453 | A | C | 1 | a0002c0002t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3215-2309A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833453 | |||||||
chr1:7833596 | A | T | 2 | a0004c0006t0001g0043 a0004c0006t0001g0045 |
2 | NA18969.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3215-2166A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833596 | |||||||
chr1:7833631 | T | C | 1 | a0001c0003t0001g0124 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3215-2131T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833631 | |||||||
chr1:7833637 | T | G | 1 | a0001c0007t0001g0253 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3215-2125T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833637 | |||||||
chr1:7833753 | G | A | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215-2009G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833753 | |||||||
chr1:7833803 | C | T | 1 | a0003c0005t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3215-1959C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833803 | |||||||
chr1:7834007 | C | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3215-1755C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834007 | |||||||
chr1:7834067 | C | T | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3215-1695C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834067 | |||||||
chr1:7834131 | A | G | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3215-1631A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834131 | |||||||
chr1:7834140 | A | C | 1 | a0003c0005t0001g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3215-1622A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834140 | |||||||
chr1:7834162 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3215-1600C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834162 | |||||||
chr1:7834167 | G | A | 2 | a0001c0007t0001g0251 a0001c0007t0001g0256 |
2 | HG02056.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3215-1595G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834167 | |||||||
chr1:7834218 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3215-1544C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834218 | |||||||
chr1:7834399 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3215-1363T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834399 | |||||||
chr1:7834446 | A | G | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3215-1316A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834446 | |||||||
chr1:7834729 | A | G | 87 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(84): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3215-1033A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834729 | |||||||
chr1:7834820 | T | A | 212 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(209): Show |
223 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.3215-942T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834820 | |||||||
chr1:7834830 | TAAAC | T | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3215-928_3215-925d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7834830 | ||||||
chr1:7834905 | A | C | 2 | a0004c0006t0001g0031 a0004c0006t0001g0032 |
2 | HG02293.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3215-857A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834905 | |||||||
chr1:7834927 | G | A | 1 | a0001c0018t0001g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3215-835G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834927 | |||||||
chr1:7834941 | C | G | 1 | a0001c0003t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3215-821C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834941 | |||||||
chr1:7834955 | C | T | 13 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(10): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3215-807C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834955 | |||||||
chr1:7834960 | G | T | 1 | a0002c0012t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3215-802G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834960 | |||||||
chr1:7835009 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(46): Show |
56 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.3215-753A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835009 | |||||||
chr1:7835217 | C | T | 2 | a0001c0003t0001g0138 a0001c0003t0001g0139 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3215-545C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835217 | |||||||
chr1:7835218 | G | A | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3215-544G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835218 | |||||||
chr1:7835262 | A | G | 1 | a0003c0005t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3215-500A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835262 | |||||||
chr1:7835358 | G | T | 30 | a0003c0005t0001g0010 a0003c0005t0001g0012 a0003c0005t0001g0063 others(27): Show |
32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3215-404G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835358 | |||||||
chr1:7835449 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3215-313G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835449 | |||||||
chr1:7835512 | G | A | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3215-250G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835512 | |||||||
chr1:7836012 | T | C | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3398+67T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836012 | |||||||
chr1:7836061 | G | A | 1 | a0001c0001t0018g0351 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3398+116G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836061 | |||||||
chr1:7836122 | C | T | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3398+177C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836122 | |||||||
chr1:7836157 | G | C | 130 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(127): Show |
134 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.3398+212G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836157 | |||||||
chr1:7836211 | A | T | 1 | a0001c0004t0001g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3398+266A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836211 | |||||||
chr1:7836395 | T | C | 5 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0067 others(2): Show |
5 | HG02717.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.3398+450T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836395 | |||||||
chr1:7836440 | A | G | 1 | a0010c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+495A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836440 | |||||||
chr1:7836781 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3399-218A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836781 | |||||||
chr1:7837168 | G | A | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3549+19G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837168 | |||||||
chr1:7837197 | G | A | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.3549+48G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837197 | |||||||
chr1:7837280 | A | G | 1 | a0001c0004t0011g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3549+131A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837280 | |||||||
chr1:7837411 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0331 |
2 | NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3549+262G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837411 | |||||||
chr1:7837415 | T | G | 1 | a0002c0002t0001g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3549+266T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837415 | |||||||
chr1:7837426 | G | A | 1 | a0001c0021t0005g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3549+277G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837426 | |||||||
chr1:7837489 | G | A | 1 | a0003c0005t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3549+340G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837489 | |||||||
chr1:7837555 | A | G | 1 | a0011c0017t0017g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3549+406A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837555 | |||||||
chr1:7837562 | A | T | 13 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(10): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3549+413A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837562 | |||||||
chr1:7837759 | T | C | 3 | a0002c0012t0001g0178 a0002c0012t0001g0179 a0002c0012t0001g0180 |
3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3549+610T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837759 | |||||||
chr1:7837826 | C | T | 6 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0067 others(3): Show |
6 | HG02257.hp2 HG02717.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3549+677C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837826 | |||||||
chr1:7837834 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3549+685G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837834 | |||||||
chr1:7837837 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0369 |
2 | HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.3549+688G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837837 | |||||||
chr1:7837869 | C | T | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3549+720C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837869 | |||||||
chr1:7837928 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(44): Show |
54 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.3549+779G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837928 | |||||||
chr1:7838046 | A | G | 3 | a0001c0001t0001g0321 a0001c0011t0001g0025 a0001c0011t0001g0330 |
4 | NA18980.hp1 NA19011.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3549+897A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838046 | |||||||
chr1:7838062 | C | CGT | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3549+928_3549+929d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7838062 | ||||||
chr1:7838095 | A | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3549+946A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838095 | |||||||
chr1:7838678 | G | A | 123 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(120): Show |
127 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.3549+1529G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838678 | |||||||
chr1:7838715 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3549+1566A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838715 | |||||||
chr1:7838765 | G | T | 4 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3549+1616G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838765 | |||||||
chr1:7838870 | A | G | 1 | a0001c0003t0001g0132 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3549+1721A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838870 | |||||||
chr1:7838904 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0267 others(1): Show |
5 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.3549+1755G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838904 | |||||||
chr1:7838961 | GACTT | G | 31 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(28): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3549+1817_3549+182 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7838961 | ||||||
chr1:7838967 | C | T | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3549+1818C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838967 | |||||||
chr1:7839006 | GA | G | 70 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0019 others(67): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3549+1858delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839006 | |||||||
chr1:7839009 | T | A | 1 | a0001c0004t0002g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3549+1860T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839009 | |||||||
chr1:7839016 | T | C | 1 | a0001c0004t0001g0162 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3549+1867T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839016 | |||||||
chr1:7839138 | G | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0266 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3549+1989G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839138 | |||||||
chr1:7839166 | C | G | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.3549+2017C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839166 | |||||||
chr1:7839277 | A | C | 1 | a0001c0021t0005g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3549+2128A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839277 | |||||||
chr1:7839280 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3549+2131C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839280 | |||||||
chr1:7839281 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3549+2132G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839281 | |||||||
chr1:7839438 | A | G | 1 | a0002c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3549+2289A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839438 | |||||||
chr1:7839476 | T | G | 1 | a0002c0002t0001g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3549+2327T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839476 | |||||||
chr1:7839485 | G | A | 1 | a0002c0002t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3549+2336G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839485 | |||||||
chr1:7839617 | T | C | 4 | a0002c0013t0001g0094 a0002c0013t0005g0097 a0002c0013t0005g0098 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3549+2468T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839617 | |||||||
chr1:7839676 | T | C | 2 | a0002c0002t0001g0209 a0002c0002t0001g0212 |
2 | HG01123.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3549+2527T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839676 | |||||||
chr1:7839759 | C | T | 1 | a0001c0003t0001g0113 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3549+2610C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839759 | |||||||
chr1:7839879 | G | GACA | 27 | a0003c0005t0001g0010 a0003c0005t0001g0069 a0003c0005t0001g0070 others(24): Show |
28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.3549+2731_3549+273 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7839879 | ||||||
chr1:7839900 | C | A | 4 | a0001c0009t0001g0290 a0001c0009t0001g0302 a0001c0009t0001g0317 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3549+2751C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839900 | |||||||
chr1:7840266 | T | G | 1 | a0001c0007t0001g0253 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3550-2406T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840266 | |||||||
chr1:7840334 | TA | T | 3 | a0001c0003t0001g0139 a0004c0006t0001g0049 a0004c0006t0001g0057 |
3 | HG01257.hp1 HG03490.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.3550-2337delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840334 | |||||||
chr1:7840335 | A | AT | 17 | a0002c0002t0001g0017 a0002c0002t0001g0189 a0002c0002t0001g0191 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3550-2326dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7840335 | ||||||
chr1:7840335 | A | T | 120 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(117): Show |
124 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.3550-2337A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840335 | |||||||
chr1:7840339 | T | G | 1 | a0004c0006t0001g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3550-2333T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840339 | |||||||
chr1:7840470 | C | T | 1 | a0005c0024t0014g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3550-2202C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840470 | |||||||
chr1:7840498 | C | T | 1 | a0002c0002t0001g0065 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3550-2174C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840498 | |||||||
chr1:7840648 | T | A | 1 | a0001c0001t0018g0351 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3550-2024T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840648 | |||||||
chr1:7840689 | C | T | 1 | a0002c0002t0001g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3550-1983C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840689 | |||||||
chr1:7840701 | G | C | 4 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3550-1971G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840701 | |||||||
chr1:7840774 | A | AT | 8 | a0001c0001t0001g0310 a0001c0003t0001g0147 a0001c0004t0001g0023 others(5): Show |
9 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3550-1885dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7840774 | ||||||
chr1:7840887 | C | T | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3550-1785C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840887 | |||||||
chr1:7840908 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3550-1764A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840908 | |||||||
chr1:7840978 | G | T | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3550-1694G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840978 | |||||||
chr1:7840997 | T | C | 1 | a0002c0002t0001g0244 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3550-1675T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840997 | |||||||
chr1:7841288 | A | AT | 100 | a0001c0001t0001g0334 a0001c0001t0001g0346 a0001c0021t0005g0096 others(97): Show |
104 | HG00408.hp2 HG00642.hp2 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.3550-1370dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7841288 | ||||||
chr1:7841288 | A | ATT | 61 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(58): Show |
62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3550-1371_3550-137 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7841288 | ||||||
chr1:7841369 | A | G | 69 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(66): Show |
70 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.3550-1303A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841369 | |||||||
chr1:7841484 | G | C | 1 | a0012c0025t0001g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3550-1188G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841484 | |||||||
chr1:7841587 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0348 |
2 | NA18961.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3550-1085C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841587 | |||||||
chr1:7841697 | A | G | 2 | a0001c0004t0001g0014 a0001c0004t0001g0166 |
3 | NA18946.hp1 NA18956.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3550-975A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841697 | |||||||
chr1:7841785 | T | C | 2 | a0008c0015t0001g0059 a0008c0015t0001g0060 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.3550-887T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841785 | |||||||
chr1:7841826 | A | G | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3550-846A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841826 | |||||||
chr1:7841828 | T | C | 62 | a0001c0003t0001g0011 a0001c0003t0001g0068 a0001c0003t0001g0099 others(59): Show |
63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3550-844T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841828 | |||||||
chr1:7841935 | T | C | 367 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(364): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3550-737T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841935 | |||||||
chr1:7842129 | T | A | 1 | a0002c0020t0001g0355 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3550-543T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842129 | |||||||
chr1:7842171 | A | G | 87 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(84): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3550-501A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842171 | |||||||
chr1:7842306 | G | A | 4 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3550-366G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842306 | |||||||
chr1:7842407 | A | G | 6 | a0002c0002t0001g0230 a0002c0002t0001g0231 a0002c0002t0001g0241 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3550-265A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842407 | |||||||
chr1:7842414 | C | T | 25 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0015 others(22): Show |
32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3550-258C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842414 | |||||||
chr1:7842499 | C | CA | 10 | a0001c0004t0002g0001 a0001c0004t0002g0164 a0001c0004t0002g0169 others(7): Show |
13 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.3550-162dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7842499 | ||||||
chr1:7842499 | C | CAA | 30 | a0001c0021t0005g0096 a0004c0006t0001g0009 a0004c0006t0001g0029 others(27): Show |
31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.3550-163_3550-162d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7842499 | ||||||
chr1:7842511 | T | A | 2 | a0002c0002t0001g0017 a0002c0002t0001g0189 |
3 | HG00733.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.3550-161T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842511 | |||||||
chr1:7842598 | A | C | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3550-74A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842598 | |||||||
chr1:7842655 | T | C | 2 | a0001c0001t0001g0026 a0015c0030t0001g0026 |
2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3550-17T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842655 |