Item | Value |
---|---|
geneid | 22796 |
ensemblid | ENSG00000135775.14 |
hgncid | 6546 |
symbol | COG2 |
name | component of oligomeric golgi complex 2 |
refseq_nuc | NM_007357.3 |
refseq_prot | NP_031383.1 |
ensembl_nuc | ENST00000366669.9 |
ensembl_prot | ENSP00000355629.4 |
mane_status | MANE Select |
chr | chr1 |
start | 230642481 |
end | 230693982 |
strand | + |
ver | v1.2 |
region | chr1:230642481-230693982 |
region5000 | chr1:230637481-230698982 |
regionname0 | COG2_chr1_230642481_230693982 |
regionname5000 | COG2_chr1_230637481_230698982 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 738 | 320 | 70 | 55 | 149 | 14 | 31 | 113 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0002 | 0/0 | 738 | 43 | 3 | 9 | 21 | 4 | 6 | 17 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0003 | 0/1 | 738 | 30 | 11 | 2 | 14 | 0 | 2 | 11 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0004 | 0/0 | 738 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0005 | 0/0 | 738 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0006 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0007 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0008 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0009 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0010 | 0/0 | 738 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
a0011 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | MEKSR others(733): Show |
chr1 | 230637481 | 230698982 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2214 | 303 | 59 | 54 | 146 | 13 | 30 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0005 | 0/0 | 2214 | 7 | 6 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0007 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0008 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0010 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0011 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0015 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0016 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0017 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0001c0018 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0002c0002 | 0/0 | 2214 | 34 | 3 | 9 | 12 | 4 | 6 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0002c0004 | 0/0 | 2214 | 9 | 0 | 0 | 9 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0003c0003 | 0/1 | 2214 | 29 | 11 | 2 | 14 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0003c0012 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0004c0006 | 0/0 | 2214 | 5 | 4 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0005c0013 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0005c0014 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0006c0019 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0007c0021 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0008c0020 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0009c0023 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0010c0022 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 | ||
a0011c0009 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGGA others(2209): Show |
chr1 | 230637481 | 230698982 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2932 | 89 | 27 | 22 | 23 | 9 | 7 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0002 | 0/0 | 2931 | 62 | 13 | 5 | 29 | 3 | 12 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0003 | 0/0 | 2931 | 53 | 1 | 13 | 36 | 0 | 3 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0004 | 0/0 | 2930 | 59 | 14 | 5 | 36 | 1 | 3 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2925): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0005 | 0/0 | 2932 | 27 | 0 | 8 | 14 | 0 | 5 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0006 | 0/0 | 2931 | 8 | 0 | 1 | 7 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0008 | 0/0 | 2932 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0009 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0001c0001t0010 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0005t0001 | 0/0 | 2932 | 6 | 5 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0005t0005 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0007t0001 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0007t0002 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0001c0008t0001 | 0/0 | 2932 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0010t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0011t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0015t0005 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0001c0016t0002 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0001c0017t0004 | 0/0 | 2930 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2925): Show |
chr1 | 230637481 | 230698982 |
a0001c0018t0008 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0002c0002t0001 | 0/0 | 2932 | 33 | 3 | 9 | 11 | 4 | 6 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0002c0002t0003 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0002c0004t0001 | 0/0 | 2932 | 9 | 0 | 0 | 9 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0003c0003t0001 | 0/0 | 2932 | 19 | 10 | 0 | 8 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0003c0003t0002 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0003c0003t0003 | 0/1 | 2931 | 2 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0003c0003t0005 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0003c0003t0007 | 0/0 | 2929 | 6 | 0 | 0 | 6 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2924): Show |
chr1 | 230637481 | 230698982 |
a0003c0012t0001 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0004c0006t0003 | 0/0 | 2931 | 5 | 4 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0005c0013t0007 | 0/0 | 2929 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2924): Show |
chr1 | 230637481 | 230698982 |
a0005c0014t0001 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0006c0019t0002 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
a0007c0021t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0008c0020t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0009c0023t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0010c0022t0001 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2927): Show |
chr1 | 230637481 | 230698982 |
a0011c0009t0003 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | ATGTT others(2926): Show |
chr1 | 230637481 | 230698982 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0003 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0006 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0013 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0001 | 0/0 | 7 | 0 | 3 | 2 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0009g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0010g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0005t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0005t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0007t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0008t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0011t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0015t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0016t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0017t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0018t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0004t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0004t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0004t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0003g0050 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0007g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0003t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0012t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0006t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0006t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0006t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0006t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0006t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0005c0013t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0005c0014t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0006c0019t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0007c0021t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0008c0020t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0009c0023t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0010c0022t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0011c0009t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0098 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0105 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00140 | hp1 | a0001 | c0015 | t0005 | g0065 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0215 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00423 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00438 | hp2 | a0003 | c0003 | t0001 | g0273 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0270 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00597 | hp2 | a0002 | c0004 | t0001 | g0010 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00639 | hp1 | a0003 | c0003 | t0003 | g0050 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01106 | hp2 | a0006 | c0019 | t0002 | g0186 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0047 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01109 | hp2 | a0003 | c0003 | t0002 | g0201 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0078 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0173 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01261 | hp1 | a0004 | c0006 | t0003 | g0268 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0131 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0075 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0066 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02027 | hp2 | a0002 | c0004 | t0001 | g0113 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02129 | hp2 | a0005 | c0014 | t0001 | g0087 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0062 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02280 | hp1 | a0001 | c0010 | t0001 | g0048 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02572 | hp2 | a0001 | c0005 | t0005 | g0090 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02622 | hp1 | a0004 | c0006 | t0003 | g0264 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0269 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02895 | hp1 | a0001 | c0018 | t0008 | g0116 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02896 | hp1 | a0003 | c0003 | t0001 | g0275 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0267 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0051 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02970 | hp1 | a0007 | c0021 | t0001 | g0092 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02970 | hp2 | a0003 | c0003 | t0001 | g0051 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03041 | hp1 | a0008 | c0020 | t0001 | g0091 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03130 | hp1 | a0001 | c0005 | t0001 | g0048 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03139 | hp1 | a0001 | c0011 | t0001 | g0093 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03139 | hp2 | a0003 | c0003 | t0001 | g0262 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0118 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03209 | hp2 | a0001 | c0005 | t0001 | g0244 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03225 | hp1 | a0009 | c0023 | t0001 | g0241 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03239 | hp1 | a0010 | c0022 | t0001 | g0297 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03516 | hp2 | a0004 | c0006 | t0003 | g0251 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0305 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0144 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03669 | hp2 | a0001 | c0017 | t0004 | g0203 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0176 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0257 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0080 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0031 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04199 | hp1 | a0003 | c0012 | t0001 | g0258 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18522 | hp2 | a0001 | c0005 | t0001 | g0245 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | CHB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | CHB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18906 | hp1 | a0003 | c0003 | t0001 | g0178 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18906 | hp2 | a0004 | c0006 | t0003 | g0265 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18942 | hp2 | a0003 | c0003 | t0001 | g0271 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18947 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18956 | hp1 | a0001 | c0007 | t0002 | g0208 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18957 | hp2 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18960 | hp1 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18966 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18967 | hp2 | a0003 | c0003 | t0007 | g0049 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18974 | hp1 | a0003 | c0003 | t0007 | g0254 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18979 | hp1 | a0002 | c0004 | t0001 | g0038 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18979 | hp2 | a0005 | c0013 | t0007 | g0252 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18981 | hp1 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18984 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18988 | hp2 | a0002 | c0004 | t0001 | g0010 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18990 | hp1 | a0003 | c0003 | t0007 | g0255 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18991 | hp2 | a0001 | c0016 | t0002 | g0161 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18994 | hp1 | a0003 | c0003 | t0007 | g0274 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19000 | hp2 | a0003 | c0003 | t0007 | g0253 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19002 | hp2 | a0001 | c0007 | t0001 | g0046 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19003 | hp2 | a0002 | c0004 | t0001 | g0010 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0272 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19010 | hp1 | a0003 | c0003 | t0007 | g0049 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19011 | hp2 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19030 | hp1 | a0003 | c0003 | t0005 | g0266 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19043 | hp2 | a0001 | c0008 | t0001 | g0279 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19054 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19065 | hp2 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0221 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19076 | hp1 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19079 | hp1 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19091 | hp1 | a0002 | c0004 | t0001 | g0038 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20129 | hp1 | a0001 | c0008 | t0001 | g0278 | AFR | ASW | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20129 | hp2 | a0001 | c0005 | t0001 | g0047 | AFR | ASW | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0013 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0115 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0129 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG06807 | hp2 | a0011 | c0009 | t0003 | g0089 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20300 | hp1 | a0001 | c0005 | t0001 | g0243 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA21309 | hp2 | a0004 | c0006 | t0003 | g0256 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
homoSapiens | chm13v2 | a0003 | c0003 | t0003 | g0050 | REF | REF | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230659609 | A | G | 1 | a0009 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.218A>G | p.Asn73Ser | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/18 | 344/2932 | 218/2217 | 73/738 | chr1 | 230659609 | |||
chr1:230663213 | A | G | 1 | a0010 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.373A>G | p.Lys125Glu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/18 | 499/2932 | 373/2217 | 125/738 | chr1 | 230663213 | |||
chr1:230671550 | A | G | 1 | a0007 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.809A>G | p.Asn270Ser | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/18 | 935/2932 | 809/2217 | 270/738 | chr1 | 230671550 | |||
chr1:230675010 | T | A | 4 | a0003 a0004 a0005 others(1): Show |
37 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(34): Show |
missense_variant | MODERATE | c.912T>A | p.Asn304Lys | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/18 | 1038/2932 | 912/2217 | 304/738 | chr1 | 230675010 | |||
chr1:230678922 | A | G | 3 | a0002 a0005 a0008 |
46 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(43): Show |
missense_variant | MODERATE | c.1036A>G | p.Ile346Val | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/18 | 1162/2932 | 1036/2217 | 346/738 | chr1 | 230678922 | |||
chr1:230687082 | C | T | 1 | a0008 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1528C>T | p.Arg510Cys | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/18 | 1654/2932 | 1528/2217 | 510/738 | chr1 | 230687082 | |||
chr1:230687086 | C | G | 1 | a0006 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1532C>G | p.Thr511Ser | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/18 | 1658/2932 | 1532/2217 | 511/738 | chr1 | 230687086 | |||
chr1:230688533 | G | A | 2 | a0004 a0011 |
6 | HG01261.hp1 HG02622.hp1 HG03516.hp2 others(3): Show |
missense_variant | MODERATE | c.1765G>A | p.Val589Ile | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/18 | 1891/2932 | 1765/2217 | 589/738 | chr1 | 230688533 | |||
chr1:230693393 | A | G | 5 | a0001 a0002 a0003 others(2): Show |
159 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
stop_retained_variant | LOW | c.2217A>G | p.Ter739Ter | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 2343/2932 | 2217/2217 | 739/738 | chr1 | 230693393 | |||
chr1:230693981 | CA | C | 5 | a0001 a0002 a0003 others(2): Show |
121 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
splice_region_variant | LOW | c.*589delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | chr1 | 230693981 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230659574 | C | T | 1 | a0001c0008 | 2 | NA19043.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.183C>T | p.Val61Val | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/18 | 309/2932 | 183/2217 | 61/738 | chr1 | 230659574 | |||
chr1:230660787 | T | G | 3 | a0001c0005 a0001c0010 a0011c0009 |
9 | HG01109.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.264T>G | p.Leu88Leu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/18 | 390/2932 | 264/2217 | 88/738 | chr1 | 230660787 | |||
chr1:230668757 | C | T | 1 | a0001c0008 | 2 | NA19043.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.567C>T | p.Gly189Gly | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/18 | 693/2932 | 567/2217 | 189/738 | chr1 | 230668757 | |||
chr1:230671587 | T | C | 1 | a0001c0011 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.846T>C | p.Phe282Phe | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/18 | 972/2932 | 846/2217 | 282/738 | chr1 | 230671587 | |||
chr1:230688469 | G | A | 1 | a0001c0007 | 2 | NA18956.hp1 NA19002.hp2 |
synonymous_variant | LOW | c.1701G>A | p.Leu567Leu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/18 | 1827/2932 | 1701/2217 | 567/738 | chr1 | 230688469 | |||
chr1:230688508 | C | T | 1 | a0001c0018 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1740C>T | p.Phe580Phe | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/18 | 1866/2932 | 1740/2217 | 580/738 | chr1 | 230688508 | |||
chr1:230690130 | C | T | 1 | a0001c0010 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1911C>T | p.Gly637Gly | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/18 | 2037/2932 | 1911/2217 | 637/738 | chr1 | 230690130 | |||
chr1:230691426 | G | A | 1 | a0001c0015 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.1977G>A | p.Lys659Lys | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/18 | 2103/2932 | 1977/2217 | 659/738 | chr1 | 230691426 | |||
chr1:230691483 | C | T | 1 | a0001c0017 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.2034C>T | p.Pro678Pro | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/18 | 2160/2932 | 2034/2217 | 678/738 | chr1 | 230691483 | |||
chr1:230691486 | C | T | 1 | a0003c0012 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.2037C>T | p.Val679Val | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/18 | 2163/2932 | 2037/2217 | 679/738 | chr1 | 230691486 | |||
chr1:230693342 | C | T | 3 | a0001c0016 a0002c0004 a0005c0014 |
11 | HG00597.hp2 HG02027.hp2 HG02129.hp2 others(8): Show |
synonymous_variant | LOW | c.2166C>T | p.Leu722Leu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 2292/2932 | 2166/2217 | 722/738 | chr1 | 230693342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230642497 | AC | A | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(6): Show |
136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
5_prime_UTR_variant | MODIFIER | c.-104delC | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/18 | 104 | INFO_REALIGN_3_PRIME | chr1 | 230642497 | |||||
chr1:230642499 | C | T | 1 | a0001c0001t0010 | 1 | NA19068.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/18 | 108 | chr1 | 230642499 | ||||||
chr1:230693530 | C | T | 2 | a0001c0001t0008 a0001c0018t0008 |
3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*137C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 137 | chr1 | 230693530 | ||||||
chr1:230693551 | C | T | 1 | a0001c0001t0009 | 2 | HG02976.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*158C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 158 | chr1 | 230693551 | ||||||
chr1:230693951 | ACCT | A | 2 | a0003c0003t0007 a0005c0013t0007 |
7 | NA18967.hp2 NA18974.hp1 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*562_*564delCCT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 562 | INFO_REALIGN_3_PRIME | chr1 | 230693951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230642700 | C | T | 1 | a0003c0003t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72+22C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642700 | |||||||
chr1:230642745 | G | C | 275 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(272): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.72+67G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642745 | |||||||
chr1:230642770 | C | T | 1 | a0001c0001t0005g0281 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.72+92C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642770 | |||||||
chr1:230642785 | G | T | 1 | a0001c0001t0004g0280 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.72+107G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642785 | |||||||
chr1:230642799 | C | G | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+121C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642799 | |||||||
chr1:230643085 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.72+407C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643085 | |||||||
chr1:230643133 | G | A | 42 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(39): Show |
56 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.72+455G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643133 | |||||||
chr1:230643327 | T | G | 43 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(40): Show |
57 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.72+649T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643327 | |||||||
chr1:230643520 | G | T | 73 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(70): Show |
89 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.72+842G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643520 | |||||||
chr1:230643589 | G | GTTTTCTA others(1): Show |
269 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(266): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.72+918_72+919insTT others(6): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230643589 | ||||||
chr1:230643664 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.72+986T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643664 | |||||||
chr1:230644008 | G | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(42): Show |
59 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.72+1330G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644008 | |||||||
chr1:230644175 | G | A | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72+1497G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644175 | |||||||
chr1:230644229 | G | C | 71 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(68): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.72+1551G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644229 | |||||||
chr1:230644242 | G | T | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72+1564G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644242 | |||||||
chr1:230644248 | A | G | 73 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(70): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+1570A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644248 | |||||||
chr1:230644262 | A | G | 1 | a0001c0001t0005g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.72+1584A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644262 | |||||||
chr1:230644489 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+1811G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644489 | |||||||
chr1:230644493 | G | T | 1 | a0001c0001t0004g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+1815G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644493 | |||||||
chr1:230644589 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.72+1911C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644589 | |||||||
chr1:230644783 | T | G | 1 | a0002c0002t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72+2105T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644783 | |||||||
chr1:230644802 | A | G | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+2124A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644802 | |||||||
chr1:230644825 | G | A | 268 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(265): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.72+2147G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644825 | |||||||
chr1:230644851 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72+2173G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644851 | |||||||
chr1:230644859 | G | T | 1 | a0001c0001t0004g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.72+2181G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644859 | |||||||
chr1:230644978 | T | G | 1 | a0001c0001t0002g0121 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.72+2300T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644978 | |||||||
chr1:230644997 | A | G | 31 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(28): Show |
33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.72+2319A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644997 | |||||||
chr1:230645233 | CA | C | 127 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(124): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.72+2578delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230645233 | ||||||
chr1:230645233 | CAA | C | 167 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0039 others(164): Show |
218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.72+2577_72+2578del others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230645233 | ||||||
chr1:230645252 | A | G | 3 | a0002c0004t0001g0011 a0002c0004t0001g0038 a0002c0004t0001g0113 |
6 | HG02027.hp2 NA18979.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2574A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645252 | |||||||
chr1:230645253 | A | G | 165 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0039 others(162): Show |
216 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.72+2575A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645253 | |||||||
chr1:230645482 | C | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+2804C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645482 | |||||||
chr1:230645512 | T | G | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72+2834T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645512 | |||||||
chr1:230645669 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
41 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+2991T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645669 | |||||||
chr1:230645700 | C | T | 6 | a0003c0003t0001g0270 a0003c0003t0001g0271 a0003c0003t0001g0272 others(3): Show |
6 | HG00438.hp2 HG00544.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3022C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645700 | |||||||
chr1:230645728 | C | A | 1 | a0001c0001t0003g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.72+3050C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645728 | |||||||
chr1:230645728 | C | G | 270 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(267): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.72+3050C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645728 | |||||||
chr1:230645763 | G | A | 1 | a0005c0013t0007g0252 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.72+3085G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645763 | |||||||
chr1:230645792 | A | G | 307 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(304): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.72+3114A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645792 | |||||||
chr1:230645861 | C | T | 8 | a0003c0003t0001g0051 a0003c0003t0001g0263 a0003c0003t0001g0267 others(5): Show |
9 | HG01261.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+3183C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645861 | |||||||
chr1:230645881 | T | C | 275 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(272): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.72+3203T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645881 | |||||||
chr1:230645903 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.72+3225G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645903 | |||||||
chr1:230645961 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0002c0002t0001g0131 others(1): Show |
4 | HG00642.hp2 HG00741.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+3283G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645961 | |||||||
chr1:230645984 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0298 others(3): Show |
9 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+3306C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645984 | |||||||
chr1:230645995 | G | A | 117 | a0001c0001t0001g0061 a0001c0001t0001g0127 a0001c0001t0001g0171 others(114): Show |
151 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.72+3317G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645995 | |||||||
chr1:230646056 | C | T | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+3378C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646056 | |||||||
chr1:230646069 | T | G | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+3391T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646069 | |||||||
chr1:230646090 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.72+3412T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646090 | |||||||
chr1:230646248 | C | G | 2 | a0001c0001t0002g0043 a0001c0001t0002g0216 |
3 | HG01192.hp2 HG01516.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.72+3570C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646248 | |||||||
chr1:230646309 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.72+3631G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646309 | |||||||
chr1:230646624 | C | T | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72+3946C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646624 | |||||||
chr1:230646666 | C | T | 112 | a0001c0001t0001g0127 a0001c0001t0001g0171 a0001c0001t0001g0213 others(109): Show |
145 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.72+3988C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646666 | |||||||
chr1:230646701 | GA | G | 70 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(67): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.72+4030delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230646701 | ||||||
chr1:230646708 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.72+4030A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646708 | |||||||
chr1:230646894 | A | G | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72+4216A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646894 | |||||||
chr1:230646988 | G | A | 70 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(67): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.72+4310G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646988 | |||||||
chr1:230647027 | T | A | 1 | a0001c0001t0004g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+4349T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647027 | |||||||
chr1:230647070 | G | A | 2 | a0002c0002t0001g0035 a0008c0020t0001g0091 |
3 | HG01106.hp1 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.72+4392G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647070 | |||||||
chr1:230647245 | C | T | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72+4567C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647245 | |||||||
chr1:230647331 | C | T | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+4653C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647331 | |||||||
chr1:230647436 | T | A | 1 | a0001c0001t0002g0136 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.72+4758T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647436 | |||||||
chr1:230647456 | T | C | 37 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0046 others(34): Show |
50 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+4778T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647456 | |||||||
chr1:230647522 | A | C | 200 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0034 others(197): Show |
254 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.72+4844A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647522 | |||||||
chr1:230647630 | G | A | 30 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.72+4952G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647630 | |||||||
chr1:230647638 | T | C | 8 | a0001c0001t0002g0012 a0001c0001t0002g0137 a0001c0001t0002g0138 others(5): Show |
10 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+4960T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647638 | |||||||
chr1:230647700 | C | T | 1 | a0004c0006t0003g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.72+5022C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647700 | |||||||
chr1:230647776 | T | C | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5098T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647776 | |||||||
chr1:230647845 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.72+5167A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647845 | |||||||
chr1:230647857 | ACT | A | 166 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0039 others(163): Show |
217 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.72+5182_72+5183del others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230647857 | ||||||
chr1:230647903 | C | T | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5225C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647903 | |||||||
chr1:230648364 | T | C | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5686T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648364 | |||||||
chr1:230648429 | A | G | 1 | a0001c0001t0003g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72+5751A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648429 | |||||||
chr1:230648460 | A | G | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5782A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648460 | |||||||
chr1:230648488 | C | T | 2 | a0002c0004t0001g0011 a0002c0004t0001g0038 |
5 | NA18979.hp1 NA18981.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+5810C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648488 | |||||||
chr1:230648529 | C | A | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+5851C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648529 | |||||||
chr1:230648761 | C | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0120 others(14): Show |
22 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+6083C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648761 | |||||||
chr1:230648820 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.72+6142C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648820 | |||||||
chr1:230648827 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72+6149C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648827 | |||||||
chr1:230648954 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+6276A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648954 | |||||||
chr1:230649043 | G | C | 28 | a0001c0001t0001g0100 a0002c0002t0001g0004 a0002c0002t0001g0036 others(25): Show |
39 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.72+6365G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649043 | |||||||
chr1:230649059 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+6381C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649059 | |||||||
chr1:230649136 | A | T | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+6458A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649136 | |||||||
chr1:230649156 | C | T | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+6478C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649156 | |||||||
chr1:230649198 | C | T | 8 | a0001c0001t0002g0012 a0001c0001t0002g0137 a0001c0001t0002g0138 others(5): Show |
10 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+6520C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649198 | |||||||
chr1:230649218 | G | A | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+6540G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649218 | |||||||
chr1:230649535 | T | G | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72+6857T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649535 | |||||||
chr1:230649759 | C | T | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+7081C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649759 | |||||||
chr1:230650159 | A | G | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+7481A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650159 | |||||||
chr1:230650425 | A | G | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+7747A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650425 | |||||||
chr1:230650701 | G | T | 2 | a0003c0003t0001g0262 a0003c0003t0001g0275 |
2 | HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.72+8023G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650701 | |||||||
chr1:230650752 | G | A | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+8074G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650752 | |||||||
chr1:230650869 | T | G | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72+8191T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650869 | |||||||
chr1:230651202 | G | A | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-8262G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651202 | |||||||
chr1:230651221 | T | C | 271 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(268): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.73-8243T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651221 | |||||||
chr1:230651222 | G | A | 27 | a0001c0001t0001g0100 a0002c0002t0001g0004 a0002c0002t0001g0036 others(24): Show |
38 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.73-8242G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651222 | |||||||
chr1:230651684 | G | A | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-7780G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651684 | |||||||
chr1:230651701 | C | A | 30 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.73-7763C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651701 | |||||||
chr1:230651849 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.73-7615T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651849 | |||||||
chr1:230652190 | G | A | 6 | a0003c0003t0007g0049 a0003c0003t0007g0253 a0003c0003t0007g0254 others(3): Show |
7 | NA18967.hp2 NA18974.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-7274G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652190 | |||||||
chr1:230652207 | C | CAGG | 275 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(272): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.73-7256_73-7255ins others(3): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230652207 | ||||||
chr1:230652237 | C | T | 1 | a0001c0001t0006g0212 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.73-7227C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652237 | |||||||
chr1:230652238 | G | A | 1 | a0007c0021t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.73-7226G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652238 | |||||||
chr1:230652348 | C | T | 1 | a0003c0003t0007g0255 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.73-7116C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652348 | |||||||
chr1:230652349 | G | A | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-7115G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652349 | |||||||
chr1:230652431 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.73-7033C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652431 | |||||||
chr1:230652447 | A | G | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-7017A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652447 | |||||||
chr1:230652470 | A | G | 31 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(28): Show |
33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-6994A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652470 | |||||||
chr1:230652569 | G | A | 25 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.73-6895G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652569 | |||||||
chr1:230652755 | T | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0094 others(15): Show |
23 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-6709T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652755 | |||||||
chr1:230652804 | C | T | 223 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0034 others(220): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.73-6660C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652804 | |||||||
chr1:230653013 | G | A | 30 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.73-6451G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653013 | |||||||
chr1:230653073 | C | T | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02258.hp1 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.73-6391C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653073 | |||||||
chr1:230653148 | G | A | 2 | a0002c0002t0001g0248 a0002c0002t0001g0249 |
2 | NA18948.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.73-6316G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653148 | |||||||
chr1:230653221 | G | GT | 65 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0094 others(62): Show |
78 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.73-6229dupT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653221 | ||||||
chr1:230653221 | G | GTT | 10 | a0001c0001t0001g0232 a0001c0001t0002g0211 a0001c0001t0003g0227 others(7): Show |
10 | HG00438.hp2 HG02083.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-6230_73-6229dup others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653221 | ||||||
chr1:230653221 | GT | G | 28 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(25): Show |
38 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.73-6229delT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653221 | ||||||
chr1:230653234 | T | G | 2 | a0001c0005t0001g0243 a0001c0005t0001g0244 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.73-6230T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653234 | |||||||
chr1:230653235 | T | G | 47 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(44): Show |
62 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.73-6229T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653235 | |||||||
chr1:230653325 | A | G | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-6139A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653325 | |||||||
chr1:230653525 | T | TTTGATTC others(30): Show |
1 | a0003c0003t0001g0275 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.73-5917_73-5881dup others(37): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653525 | ||||||
chr1:230653525 | T | TTTGATTC others(30): Show |
269 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(266): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.73-5915_73-5914ins others(37): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653525 | ||||||
chr1:230653525 | T | TTTGATTC others(30): Show |
1 | a0001c0001t0004g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-5915_73-5914ins others(37): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653525 | ||||||
chr1:230653633 | G | A | 222 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0039 others(219): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.73-5831G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653633 | |||||||
chr1:230653661 | A | C | 1 | a0001c0001t0002g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.73-5803A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653661 | |||||||
chr1:230653701 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.73-5763T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653701 | |||||||
chr1:230653738 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73-5726C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653738 | |||||||
chr1:230653762 | T | A | 1 | a0002c0002t0001g0096 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.73-5702T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653762 | |||||||
chr1:230653838 | A | T | 1 | a0001c0001t0005g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.73-5626A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653838 | |||||||
chr1:230653855 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.73-5609T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653855 | |||||||
chr1:230653923 | C | CCTCATGA | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5539_73-5533dup others(7): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653923 | ||||||
chr1:230653946 | A | C | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5518A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653946 | |||||||
chr1:230653983 | G | C | 28 | a0001c0001t0001g0100 a0002c0002t0001g0004 a0002c0002t0001g0036 others(25): Show |
39 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-5481G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653983 | |||||||
chr1:230654038 | T | C | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5426T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654038 | |||||||
chr1:230654461 | A | G | 4 | a0001c0001t0003g0033 a0001c0001t0003g0081 a0001c0001t0003g0082 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-5003A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654461 | |||||||
chr1:230654667 | A | T | 1 | a0001c0001t0006g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.73-4797A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654667 | |||||||
chr1:230654836 | T | G | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-4628T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654836 | |||||||
chr1:230654888 | C | G | 1 | a0001c0001t0001g0289 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.73-4576C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654888 | |||||||
chr1:230654922 | C | G | 1 | a0001c0001t0003g0226 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.73-4542C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654922 | |||||||
chr1:230654947 | G | A | 30 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.73-4517G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654947 | |||||||
chr1:230655036 | C | G | 1 | a0001c0001t0001g0026 | 3 | HG00741.hp2 HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.73-4428C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655036 | |||||||
chr1:230655317 | A | G | 31 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(28): Show |
33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-4147A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655317 | |||||||
chr1:230655345 | A | G | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.73-4119A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655345 | |||||||
chr1:230655412 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0282 |
5 | HG01069.hp1 HG01175.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-4052G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655412 | |||||||
chr1:230655414 | G | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0094 others(15): Show |
23 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-4050G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655414 | |||||||
chr1:230655606 | G | A | 1 | a0001c0017t0004g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73-3858G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655606 | |||||||
chr1:230655691 | A | T | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-3773A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655691 | |||||||
chr1:230655882 | G | A | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.73-3582G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655882 | |||||||
chr1:230655891 | T | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0063 others(37): Show |
53 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.73-3573T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655891 | |||||||
chr1:230655900 | T | C | 1 | a0001c0017t0004g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73-3564T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655900 | |||||||
chr1:230655917 | C | G | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-3547C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655917 | |||||||
chr1:230656092 | G | A | 1 | a0011c0009t0003g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-3372G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656092 | |||||||
chr1:230656153 | T | C | 1 | a0007c0021t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.73-3311T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656153 | |||||||
chr1:230656174 | C | T | 1 | a0003c0003t0002g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.73-3290C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656174 | |||||||
chr1:230656178 | A | G | 18 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0094 others(15): Show |
23 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-3286A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656178 | |||||||
chr1:230656286 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73-3178C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656286 | |||||||
chr1:230656312 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.73-3152G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656312 | |||||||
chr1:230656431 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-3033G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656431 | |||||||
chr1:230656432 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-3032G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656432 | |||||||
chr1:230656438 | G | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(37): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.73-3026G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656438 | |||||||
chr1:230656496 | A | G | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(37): Show |
54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.73-2968A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656496 | |||||||
chr1:230656631 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0008g0115 a0001c0001t0008g0118 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-2833T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656631 | |||||||
chr1:230656778 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.73-2686A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656778 | |||||||
chr1:230657065 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-2399T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657065 | |||||||
chr1:230657165 | A | G | 1 | a0003c0003t0007g0254 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.73-2299A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657165 | |||||||
chr1:230657201 | G | GGT | 224 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0034 others(221): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.73-2263_73-2262ins others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657201 | |||||||
chr1:230657204 | T | C | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-2260T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657204 | |||||||
chr1:230657261 | G | A | 194 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0034 others(191): Show |
247 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.73-2203G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657261 | |||||||
chr1:230657426 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-2038G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657426 | |||||||
chr1:230657641 | G | C | 28 | a0001c0001t0001g0100 a0002c0002t0001g0004 a0002c0002t0001g0036 others(25): Show |
39 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-1823G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657641 | |||||||
chr1:230657686 | G | A | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1778G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657686 | |||||||
chr1:230657693 | T | C | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1771T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657693 | |||||||
chr1:230657707 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0287 a0001c0001t0001g0288 |
5 | HG00140.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-1757C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657707 | |||||||
chr1:230657768 | T | C | 31 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(28): Show |
33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-1696T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657768 | |||||||
chr1:230657844 | C | T | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1620C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657844 | |||||||
chr1:230657860 | C | T | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1604C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657860 | |||||||
chr1:230657884 | C | G | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1580C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657884 | |||||||
chr1:230657914 | G | A | 22 | a0003c0003t0001g0257 a0003c0003t0001g0259 a0003c0003t0001g0260 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.73-1550G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657914 | |||||||
chr1:230658103 | TC | T | 39 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0063 others(36): Show |
52 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.73-1358delC | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230658103 | ||||||
chr1:230658208 | T | C | 1 | a0001c0001t0005g0028 | 2 | NA18978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.73-1256T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658208 | |||||||
chr1:230658290 | T | C | 1 | a0001c0001t0001g0023 | 3 | HG01243.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.73-1174T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658290 | |||||||
chr1:230658355 | T | C | 1 | a0002c0002t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-1109T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658355 | |||||||
chr1:230658408 | G | C | 30 | a0001c0001t0001g0100 a0001c0008t0001g0278 a0001c0008t0001g0279 others(27): Show |
41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1056G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658408 | |||||||
chr1:230658433 | C | T | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.73-1031C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658433 | |||||||
chr1:230658479 | T | C | 2 | a0002c0002t0001g0036 a0002c0002t0001g0098 |
3 | HG00099.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.73-985T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658479 | |||||||
chr1:230658480 | G | A | 223 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0039 others(220): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.73-984G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658480 | |||||||
chr1:230658504 | G | T | 1 | a0002c0002t0001g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.73-960G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658504 | |||||||
chr1:230658517 | G | T | 1 | a0004c0006t0003g0268 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.73-947G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658517 | |||||||
chr1:230658683 | C | T | 2 | a0001c0001t0003g0224 a0001c0001t0003g0225 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.73-781C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658683 | |||||||
chr1:230658835 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.73-629A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658835 | |||||||
chr1:230659038 | A | G | 2 | a0003c0003t0001g0260 a0003c0003t0001g0261 |
2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.73-426A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659038 | |||||||
chr1:230659090 | A | T | 1 | a0011c0009t0003g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-374A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659090 | |||||||
chr1:230659156 | T | A | 3 | a0002c0002t0001g0096 a0002c0002t0001g0099 a0002c0002t0001g0109 |
3 | NA18961.hp1 NA18964.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.73-308T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659156 | |||||||
chr1:230659431 | T | C | 243 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(240): Show |
310 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.73-33T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659431 | |||||||
chr1:230659795 | A | G | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+170A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230659795 | |||||||
chr1:230659895 | A | G | 196 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0034 others(193): Show |
249 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.234+270A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230659895 | |||||||
chr1:230660212 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235-546G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660212 | |||||||
chr1:230660227 | G | A | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-531G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660227 | |||||||
chr1:230660267 | A | G | 2 | a0001c0001t0002g0198 a0001c0001t0009g0042 |
3 | HG02976.hp2 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.235-491A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660267 | |||||||
chr1:230660382 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-376T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660382 | |||||||
chr1:230660468 | A | G | 1 | a0001c0001t0003g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.235-290A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660468 | |||||||
chr1:230660494 | C | T | 30 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.235-264C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660494 | |||||||
chr1:230660580 | A | G | 41 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(38): Show |
55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.235-178A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660580 | |||||||
chr1:230660629 | A | C | 113 | a0001c0001t0001g0127 a0001c0001t0001g0171 a0001c0001t0001g0213 others(110): Show |
146 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.235-129A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660629 | |||||||
chr1:230660633 | A | G | 1 | a0003c0003t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235-125A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660633 | |||||||
chr1:230660995 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.300+172G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230660995 | |||||||
chr1:230661126 | CAT | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0282 |
5 | HG01069.hp1 HG01175.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+306_300+307del others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 230661126 | ||||||
chr1:230661320 | G | A | 273 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(270): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.300+497G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661320 | |||||||
chr1:230661354 | A | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+531A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661354 | |||||||
chr1:230661386 | C | T | 2 | a0003c0003t0002g0201 a0004c0006t0003g0268 |
2 | HG01109.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.300+563C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661386 | |||||||
chr1:230661490 | C | T | 1 | a0001c0001t0003g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.300+667C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661490 | |||||||
chr1:230661579 | C | A | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(21): Show |
35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.300+756C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661579 | |||||||
chr1:230661758 | A | G | 2 | a0001c0001t0002g0197 a0001c0001t0002g0210 |
2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.300+935A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661758 | |||||||
chr1:230661794 | A | G | 1 | a0001c0001t0004g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.300+971A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661794 | |||||||
chr1:230661872 | A | T | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.300+1049A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661872 | |||||||
chr1:230661944 | T | C | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.300+1121T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661944 | |||||||
chr1:230662064 | A | G | 1 | a0001c0001t0003g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-1077A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662064 | |||||||
chr1:230662209 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0302 |
3 | HG02818.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.301-932C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662209 | |||||||
chr1:230662245 | C | A | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.301-896C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662245 | |||||||
chr1:230662350 | A | G | 1 | a0001c0001t0005g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.301-791A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662350 | |||||||
chr1:230662509 | C | A | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301-632C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662509 | |||||||
chr1:230663017 | A | G | 1 | a0008c0020t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-124A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230663017 | |||||||
chr1:230663060 | C | T | 1 | a0001c0001t0009g0042 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-81C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230663060 | |||||||
chr1:230663062 | G | A | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(21): Show |
35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.301-79G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230663062 | |||||||
chr1:230663537 | T | G | 1 | a0002c0002t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.381+316T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230663537 | |||||||
chr1:230663752 | G | A | 7 | a0003c0003t0007g0049 a0003c0003t0007g0253 a0003c0003t0007g0254 others(4): Show |
8 | NA18967.hp2 NA18974.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+531G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230663752 | |||||||
chr1:230663797 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02080.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.381+576A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230663797 | |||||||
chr1:230664087 | G | A | 1 | a0003c0003t0001g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382-397G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664087 | |||||||
chr1:230664238 | C | CA | 8 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(5): Show |
9 | HG01109.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-235dupA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 230664238 | ||||||
chr1:230664371 | T | C | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-113T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664371 | |||||||
chr1:230664384 | G | A | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-100G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664384 | |||||||
chr1:230664448 | A | G | 2 | a0001c0001t0003g0224 a0001c0001t0003g0225 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.382-36A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664448 | |||||||
chr1:230664710 | T | C | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+123T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230664710 | |||||||
chr1:230665013 | T | C | 1 | a0001c0001t0001g0023 | 3 | HG01243.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.485+426T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665013 | |||||||
chr1:230665119 | C | T | 1 | a0003c0003t0007g0254 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.485+532C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665119 | |||||||
chr1:230665130 | T | C | 1 | a0003c0003t0001g0270 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.485+543T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665130 | |||||||
chr1:230665201 | A | G | 25 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.485+614A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665201 | |||||||
chr1:230665247 | G | A | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+660G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665247 | |||||||
chr1:230665283 | C | T | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+696C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665283 | |||||||
chr1:230665301 | A | G | 1 | a0003c0003t0002g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.485+714A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665301 | |||||||
chr1:230665444 | A | C | 1 | a0001c0001t0003g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.485+857A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665444 | |||||||
chr1:230665475 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+888G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665475 | |||||||
chr1:230665494 | G | A | 1 | a0001c0001t0005g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.485+907G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665494 | |||||||
chr1:230665784 | A | G | 307 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(304): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.485+1197A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665784 | |||||||
chr1:230665795 | C | T | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+1208C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665795 | |||||||
chr1:230665797 | A | T | 2 | a0001c0001t0004g0128 a0001c0001t0004g0195 |
2 | NA18994.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.485+1210A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665797 | |||||||
chr1:230665988 | G | A | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+1401G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665988 | |||||||
chr1:230666269 | C | T | 32 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(29): Show |
43 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+1682C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666269 | |||||||
chr1:230666613 | T | G | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+2026T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666613 | |||||||
chr1:230666691 | A | G | 1 | a0001c0001t0006g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486-1985A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666691 | |||||||
chr1:230666796 | A | G | 1 | a0003c0003t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-1880A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666796 | |||||||
chr1:230667116 | G | C | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-1560G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667116 | |||||||
chr1:230667125 | G | C | 1 | a0001c0001t0004g0204 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.486-1551G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667125 | |||||||
chr1:230667134 | G | T | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.486-1542G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667134 | |||||||
chr1:230667179 | G | A | 4 | a0001c0001t0004g0128 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
4 | HG02135.hp2 NA18994.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-1497G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667179 | |||||||
chr1:230667206 | C | T | 1 | a0002c0002t0001g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.486-1470C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667206 | |||||||
chr1:230667226 | C | T | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(21): Show |
35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.486-1450C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667226 | |||||||
chr1:230667328 | G | C | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.486-1348G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667328 | |||||||
chr1:230667478 | G | A | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.486-1198G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667478 | |||||||
chr1:230667534 | A | G | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-1142A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667534 | |||||||
chr1:230667716 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486-960G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667716 | |||||||
chr1:230667786 | AGGGACAT others(15): Show |
A | 2 | a0001c0001t0001g0079 a0001c0001t0005g0078 |
2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.486-887_486-866del others(22): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 230667786 | ||||||
chr1:230668072 | A | G | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.486-604A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668072 | |||||||
chr1:230668288 | T | A | 10 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(7): Show |
11 | HG01109.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-388T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668288 | |||||||
chr1:230668297 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.486-379G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668297 | |||||||
chr1:230668334 | T | A | 1 | a0001c0001t0004g0148 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.486-342T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668334 | |||||||
chr1:230668409 | G | A | 1 | a0001c0001t0004g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.486-267G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668409 | |||||||
chr1:230668426 | T | G | 1 | a0001c0001t0002g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.486-250T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668426 | |||||||
chr1:230668453 | C | T | 1 | a0003c0003t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.486-223C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668453 | |||||||
chr1:230668453 | CG | C | 30 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.486-221delG | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 230668453 | ||||||
chr1:230668607 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486-69G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668607 | |||||||
chr1:230668855 | A | G | 1 | a0001c0001t0003g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.594+71A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230668855 | |||||||
chr1:230668873 | G | A | 1 | a0003c0003t0002g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.594+89G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230668873 | |||||||
chr1:230669027 | C | T | 57 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0039 others(54): Show |
76 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.594+243C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669027 | |||||||
chr1:230669076 | A | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
8 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-280A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669076 | |||||||
chr1:230669112 | T | C | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.595-244T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669112 | |||||||
chr1:230669318 | C | G | 1 | a0001c0001t0003g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.595-38C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669318 | |||||||
chr1:230669736 | C | T | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+201C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230669736 | |||||||
chr1:230669768 | G | A | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+233G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230669768 | |||||||
chr1:230669917 | G | A | 1 | a0003c0003t0007g0255 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.774+382G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230669917 | |||||||
chr1:230670040 | G | A | 31 | a0003c0003t0001g0051 a0003c0003t0001g0257 a0003c0003t0001g0259 others(28): Show |
33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.774+505G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670040 | |||||||
chr1:230670212 | A | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0230 |
5 | HG02083.hp1 HG02165.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+677A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670212 | |||||||
chr1:230670314 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.774+779C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670314 | |||||||
chr1:230670332 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+797C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670332 | |||||||
chr1:230670568 | A | G | 1 | a0001c0001t0006g0179 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.775-948A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670568 | |||||||
chr1:230670619 | T | A | 39 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0063 others(36): Show |
52 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.775-897T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670619 | |||||||
chr1:230670629 | C | G | 2 | a0001c0008t0001g0278 a0001c0008t0001g0279 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-887C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670629 | |||||||
chr1:230670721 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.775-795G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670721 | |||||||
chr1:230670812 | C | T | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.775-704C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670812 | |||||||
chr1:230670904 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.775-612C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670904 | |||||||
chr1:230670952 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.775-564G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670952 | |||||||
chr1:230671075 | A | G | 1 | a0003c0003t0001g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.775-441A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671075 | |||||||
chr1:230671150 | C | A | 1 | a0001c0001t0005g0062 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.775-366C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671150 | |||||||
chr1:230671164 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0084 others(1): Show |
5 | HG02071.hp2 HG02129.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-352A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671164 | |||||||
chr1:230671319 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.775-197A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671319 | |||||||
chr1:230671486 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.775-30T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671486 | |||||||
chr1:230671734 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.899+94G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671734 | |||||||
chr1:230671869 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0002g0210 |
2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.899+229C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671869 | |||||||
chr1:230671946 | A | G | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.899+306A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671946 | |||||||
chr1:230671980 | T | G | 1 | a0001c0001t0004g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.899+340T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671980 | |||||||
chr1:230672185 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.899+545C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672185 | |||||||
chr1:230672254 | G | A | 1 | a0001c0008t0001g0278 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.899+614G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672254 | |||||||
chr1:230672259 | T | G | 163 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(160): Show |
215 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.899+619T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672259 | |||||||
chr1:230672303 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0003g0027 a0001c0001t0003g0059 others(2): Show |
6 | HG02071.hp1 NA18941.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.899+663G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672303 | |||||||
chr1:230672308 | A | G | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.899+668A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672308 | |||||||
chr1:230672313 | A | T | 1 | a0001c0001t0005g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.899+673A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672313 | |||||||
chr1:230672500 | C | T | 39 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0079 others(36): Show |
51 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.899+860C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672500 | |||||||
chr1:230672552 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.899+912C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672552 | |||||||
chr1:230672664 | TA | T | 196 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(193): Show |
250 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.899+1037delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr1 | 230672664 | ||||||
chr1:230672679 | G | A | 198 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(195): Show |
252 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.899+1039G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672679 | |||||||
chr1:230672698 | T | G | 1 | a0001c0001t0003g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.899+1058T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672698 | |||||||
chr1:230672701 | A | T | 1 | a0001c0001t0002g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.899+1061A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672701 | |||||||
chr1:230672812 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.899+1172T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672812 | |||||||
chr1:230672821 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.899+1181A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672821 | |||||||
chr1:230672890 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.899+1250G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672890 | |||||||
chr1:230672916 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.899+1276A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672916 | |||||||
chr1:230672922 | C | T | 1 | a0001c0001t0005g0031 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.899+1282C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672922 | |||||||
chr1:230672966 | T | A | 36 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0079 others(33): Show |
48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.899+1326T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672966 | |||||||
chr1:230672978 | T | C | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.899+1338T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672978 | |||||||
chr1:230672998 | G | T | 116 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(113): Show |
152 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.899+1358G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672998 | |||||||
chr1:230673169 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.899+1529C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673169 | |||||||
chr1:230673457 | G | A | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.900-1541G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673457 | |||||||
chr1:230673688 | T | G | 32 | a0003c0003t0001g0051 a0003c0003t0001g0178 a0003c0003t0001g0257 others(29): Show |
34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.900-1310T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673688 | |||||||
chr1:230673799 | A | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.900-1199A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673799 | |||||||
chr1:230673911 | T | A | 1 | a0001c0015t0005g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.900-1087T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673911 | |||||||
chr1:230673918 | T | C | 1 | a0001c0011t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.900-1080T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673918 | |||||||
chr1:230673944 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.900-1054G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673944 | |||||||
chr1:230673969 | A | G | 1 | a0001c0001t0004g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.900-1029A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673969 | |||||||
chr1:230674112 | A | G | 200 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(197): Show |
254 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.900-886A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674112 | |||||||
chr1:230674146 | G | A | 1 | a0001c0001t0004g0152 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.900-852G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674146 | |||||||
chr1:230674225 | T | C | 2 | a0001c0001t0004g0153 a0001c0001t0004g0154 |
2 | HG00609.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.900-773T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674225 | |||||||
chr1:230674309 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.900-689G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674309 | |||||||
chr1:230674595 | C | T | 2 | a0001c0001t0001g0127 a0001c0008t0001g0278 |
2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.900-403C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674595 | |||||||
chr1:230674616 | G | T | 35 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0079 others(32): Show |
47 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.900-382G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674616 | |||||||
chr1:230674629 | A | T | 25 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.900-369A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674629 | |||||||
chr1:230674799 | C | A | 2 | a0001c0001t0005g0031 a0001c0001t0005g0066 |
3 | HG01993.hp2 HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.900-199C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674799 | |||||||
chr1:230674873 | G | A | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.900-125G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674873 | |||||||
chr1:230675138 | C | T | 1 | a0007c0021t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+14C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675138 | |||||||
chr1:230675215 | G | C | 1 | a0002c0002t0001g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1026+91G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675215 | |||||||
chr1:230675321 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1026+197A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675321 | |||||||
chr1:230675389 | T | C | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1026+265T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675389 | |||||||
chr1:230675731 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026+607C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675731 | |||||||
chr1:230675889 | A | T | 1 | a0001c0001t0004g0126 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1026+765A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675889 | |||||||
chr1:230675970 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1026+846G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675970 | |||||||
chr1:230676142 | T | G | 1 | a0001c0001t0006g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1026+1018T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676142 | |||||||
chr1:230676292 | C | T | 275 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(272): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1026+1168C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676292 | |||||||
chr1:230676410 | T | C | 239 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(236): Show |
305 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1026+1286T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676410 | |||||||
chr1:230676436 | C | T | 36 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0079 others(33): Show |
48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1026+1312C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676436 | |||||||
chr1:230676458 | G | A | 4 | a0001c0001t0001g0127 a0003c0003t0001g0129 a0003c0003t0001g0305 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+1334G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676458 | |||||||
chr1:230676520 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1026+1396G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676520 | |||||||
chr1:230676524 | G | A | 1 | a0003c0003t0007g0274 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1026+1400G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676524 | |||||||
chr1:230676546 | A | T | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1026+1422A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676546 | |||||||
chr1:230676583 | C | T | 36 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0079 others(33): Show |
48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1026+1459C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676583 | |||||||
chr1:230676584 | A | G | 307 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(304): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1026+1460A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676584 | |||||||
chr1:230676587 | A | C | 2 | a0001c0001t0001g0127 a0001c0008t0001g0278 |
2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1026+1463A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676587 | |||||||
chr1:230676700 | T | C | 4 | a0001c0001t0003g0122 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): Show |
4 | HG02083.hp2 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+1576T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676700 | |||||||
chr1:230676712 | T | A | 163 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(160): Show |
215 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1026+1588T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676712 | |||||||
chr1:230676721 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1026+1597T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676721 | |||||||
chr1:230676729 | T | C | 1 | a0001c0008t0001g0278 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026+1605T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676729 | |||||||
chr1:230676836 | T | A | 2 | a0002c0002t0001g0106 a0002c0002t0001g0114 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1026+1712T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676836 | |||||||
chr1:230676897 | C | T | 3 | a0002c0004t0001g0011 a0002c0004t0001g0038 a0002c0004t0001g0113 |
6 | HG02027.hp2 NA18979.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+1773C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676897 | |||||||
chr1:230677080 | A | G | 25 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1027-1833A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677080 | |||||||
chr1:230677089 | T | G | 2 | a0001c0001t0003g0224 a0001c0001t0003g0225 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1027-1824T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677089 | |||||||
chr1:230677315 | C | T | 1 | a0002c0002t0001g0036 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1027-1598C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677315 | |||||||
chr1:230677344 | G | C | 25 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1027-1569G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677344 | |||||||
chr1:230677442 | C | T | 1 | a0003c0003t0001g0272 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1027-1471C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677442 | |||||||
chr1:230677465 | G | T | 1 | a0001c0001t0004g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1027-1448G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677465 | |||||||
chr1:230677533 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1027-1380A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677533 | |||||||
chr1:230677568 | A | T | 36 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0079 others(33): Show |
48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1027-1345A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677568 | |||||||
chr1:230677587 | GGCTTTAA others(16): Show |
G | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(21): Show |
35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1315_1027-129 others(27): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 230677587 | ||||||
chr1:230677637 | C | T | 30 | a0003c0003t0001g0051 a0003c0003t0001g0178 a0003c0003t0001g0257 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1027-1276C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677637 | |||||||
chr1:230677778 | T | C | 4 | a0001c0001t0003g0122 a0001c0001t0003g0156 a0001c0001t0003g0157 others(1): Show |
4 | HG02083.hp2 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-1135T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677778 | |||||||
chr1:230677892 | C | G | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(21): Show |
35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1021C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677892 | |||||||
chr1:230677959 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1027-954A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677959 | |||||||
chr1:230678058 | T | C | 2 | a0001c0005t0005g0090 a0011c0009t0003g0089 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1027-855T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678058 | |||||||
chr1:230678092 | A | G | 1 | a0001c0001t0005g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1027-821A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678092 | |||||||
chr1:230678190 | C | T | 1 | a0001c0001t0005g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1027-723C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678190 | |||||||
chr1:230678235 | C | T | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1027-678C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678235 | |||||||
chr1:230678297 | T | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-616T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678297 | |||||||
chr1:230678337 | C | T | 234 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(231): Show |
299 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1027-576C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678337 | |||||||
chr1:230678346 | C | T | 4 | a0001c0001t0004g0128 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
4 | HG02135.hp2 NA18994.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-567C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678346 | |||||||
chr1:230678685 | A | G | 25 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0218 others(22): Show |
36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1027-228A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678685 | |||||||
chr1:230678707 | C | T | 2 | a0003c0003t0001g0129 a0003c0003t0001g0305 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1027-206C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678707 | |||||||
chr1:230678884 | A | G | 3 | a0003c0003t0001g0129 a0003c0003t0001g0305 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1027-29A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678884 | |||||||
chr1:230679070 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1166+18C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679070 | |||||||
chr1:230679082 | G | A | 2 | a0001c0001t0001g0213 a0007c0021t0001g0092 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1166+30G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679082 | |||||||
chr1:230679135 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1166+83C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679135 | |||||||
chr1:230679431 | T | C | 31 | a0001c0001t0001g0024 a0001c0001t0001g0233 a0001c0001t0001g0289 others(28): Show |
49 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1166+379T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679431 | |||||||
chr1:230679438 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1166+386T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679438 | |||||||
chr1:230679451 | G | A | 75 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(72): Show |
106 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1166+399G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679451 | |||||||
chr1:230679459 | T | G | 4 | a0001c0001t0002g0139 a0001c0001t0002g0150 a0001c0008t0001g0278 others(1): Show |
4 | HG02055.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166+407T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679459 | |||||||
chr1:230679475 | G | A | 2 | a0003c0003t0001g0129 a0009c0023t0001g0241 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1166+423G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679475 | |||||||
chr1:230679630 | T | C | 229 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(226): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1166+578T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679630 | |||||||
chr1:230679658 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1166+606T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679658 | |||||||
chr1:230679670 | C | A | 7 | a0001c0001t0004g0002 a0001c0001t0004g0158 a0001c0001t0004g0160 others(4): Show |
13 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1166+618C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679670 | |||||||
chr1:230679735 | T | G | 115 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(112): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1166+683T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679735 | |||||||
chr1:230679799 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1166+747C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679799 | |||||||
chr1:230679904 | A | G | 2 | a0003c0003t0001g0051 a0003c0003t0001g0263 |
3 | HG02615.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1166+852A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679904 | |||||||
chr1:230679991 | A | G | 1 | a0004c0006t0003g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1166+939A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679991 | |||||||
chr1:230680160 | G | A | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1166+1108G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680160 | |||||||
chr1:230680377 | G | GACCCTGG others(15): Show |
37 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
49 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1166+1329_1166+135 others(26): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230680377 | ||||||
chr1:230680391 | T | TGCAGCAT others(15): Show |
5 | a0001c0001t0001g0171 a0001c0001t0001g0232 a0001c0001t0002g0043 others(2): Show |
6 | HG01168.hp2 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1166+1350_1166+135 others(26): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230680391 | ||||||
chr1:230680438 | T | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1166+1386T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680438 | |||||||
chr1:230680473 | G | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1166+1421G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680473 | |||||||
chr1:230680495 | C | T | 301 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(298): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1166+1443C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680495 | |||||||
chr1:230680511 | C | G | 1 | a0001c0001t0004g0169 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1166+1459C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680511 | |||||||
chr1:230680523 | C | T | 106 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(103): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1166+1471C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680523 | |||||||
chr1:230680651 | C | T | 1 | a0001c0001t0006g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1166+1599C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680651 | |||||||
chr1:230680694 | A | T | 29 | a0001c0001t0005g0001 a0001c0001t0005g0028 a0001c0001t0005g0031 others(26): Show |
37 | HG00140.hp1 HG00423.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1166+1642A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680694 | |||||||
chr1:230680704 | G | T | 1 | a0001c0001t0004g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1166+1652G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680704 | |||||||
chr1:230680714 | C | T | 124 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0021 others(121): Show |
166 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1166+1662C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680714 | |||||||
chr1:230680811 | T | C | 108 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(105): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1166+1759T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680811 | |||||||
chr1:230680849 | G | A | 1 | a0001c0001t0002g0164 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1166+1797G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680849 | |||||||
chr1:230680934 | T | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166+1882T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680934 | |||||||
chr1:230680999 | A | G | 128 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(125): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1166+1947A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680999 | |||||||
chr1:230681105 | C | T | 1 | a0003c0003t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1166+2053C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681105 | |||||||
chr1:230681459 | G | A | 3 | a0001c0001t0008g0115 a0001c0001t0008g0118 a0001c0018t0008g0116 |
3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1167-2115G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681459 | |||||||
chr1:230681609 | T | G | 1 | a0001c0001t0003g0224 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1167-1965T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681609 | |||||||
chr1:230681638 | G | A | 169 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(166): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1167-1936G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681638 | |||||||
chr1:230681688 | C | G | 127 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(124): Show |
169 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1167-1886C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681688 | |||||||
chr1:230681734 | C | T | 52 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0044 others(49): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1167-1840C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681734 | |||||||
chr1:230681900 | C | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1167-1674C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681900 | |||||||
chr1:230681983 | TTATCATA others(2): Show |
T | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1167-1587_1167-157 others(13): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230681983 | ||||||
chr1:230681984 | TATC | T | 165 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(162): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1167-1587_1167-158 others(7): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230681984 | ||||||
chr1:230682024 | G | C | 295 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(292): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1167-1550G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682024 | |||||||
chr1:230682026 | T | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0127 a0001c0001t0001g0292 others(9): Show |
16 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1167-1548T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682026 | |||||||
chr1:230682040 | A | G | 3 | a0001c0001t0008g0115 a0001c0001t0008g0118 a0001c0018t0008g0116 |
3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1167-1534A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682040 | |||||||
chr1:230682113 | T | G | 295 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(292): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1167-1461T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682113 | |||||||
chr1:230682342 | C | G | 1 | a0008c0020t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1167-1232C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682342 | |||||||
chr1:230682524 | A | G | 1 | a0001c0001t0002g0018 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1167-1050A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682524 | |||||||
chr1:230682558 | G | A | 106 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(103): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1167-1016G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682558 | |||||||
chr1:230682643 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1167-931C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682643 | |||||||
chr1:230682665 | G | A | 169 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(166): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1167-909G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682665 | |||||||
chr1:230682691 | T | G | 3 | a0001c0001t0008g0115 a0001c0001t0008g0118 a0001c0018t0008g0116 |
3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1167-883T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682691 | |||||||
chr1:230682879 | G | A | 106 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(103): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1167-695G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682879 | |||||||
chr1:230683095 | G | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1167-479G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230683095 | |||||||
chr1:230683125 | T | G | 1 | a0001c0001t0009g0042 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1167-449T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230683125 | |||||||
chr1:230683409 | TA | T | 141 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(138): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1167-145delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230683409 | ||||||
chr1:230683409 | TAA | T | 32 | a0001c0001t0001g0044 a0001c0001t0001g0079 a0001c0001t0001g0239 others(29): Show |
40 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1167-146_1167-145d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230683409 | ||||||
chr1:230683549 | ATTC | A | 121 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(118): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1167-16_1167-14del others(3): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230683549 | ||||||
chr1:230683733 | G | GT | 285 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(282): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1228+110dupT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230683733 | ||||||
chr1:230683733 | G | GTT | 10 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(7): Show |
11 | HG01106.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228+109_1228+110d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230683733 | ||||||
chr1:230683846 | C | A | 1 | a0003c0003t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1228+211C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230683846 | |||||||
chr1:230683896 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1228+261A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230683896 | |||||||
chr1:230683912 | C | T | 1 | a0001c0011t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1228+277C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230683912 | |||||||
chr1:230684039 | C | A | 1 | a0001c0001t0005g0281 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1228+404C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684039 | |||||||
chr1:230684039 | C | G | 120 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(117): Show |
161 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1228+404C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684039 | |||||||
chr1:230684157 | T | A | 1 | a0001c0011t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1228+522T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684157 | |||||||
chr1:230684264 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1228+629T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684264 | |||||||
chr1:230684275 | A | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(44): Show |
61 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1228+640A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684275 | |||||||
chr1:230684315 | G | T | 2 | a0001c0001t0003g0226 a0001c0001t0003g0227 |
2 | HG00673.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1228+680G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684315 | |||||||
chr1:230684476 | T | G | 295 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(292): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1229-609T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684476 | |||||||
chr1:230684477 | T | A | 295 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(292): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1229-608T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684477 | |||||||
chr1:230684546 | A | C | 112 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(109): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1229-539A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684546 | |||||||
chr1:230684605 | A | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1229-480A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684605 | |||||||
chr1:230684770 | C | G | 1 | a0001c0001t0004g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1229-315C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684770 | |||||||
chr1:230684832 | G | A | 89 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0021 others(86): Show |
122 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1229-253G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684832 | |||||||
chr1:230684859 | G | T | 121 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(118): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1229-226G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684859 | |||||||
chr1:230684884 | G | A | 124 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(121): Show |
161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1229-201G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684884 | |||||||
chr1:230685017 | C | CACATT | 47 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(44): Show |
61 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1229-66_1229-62dup others(5): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230685017 | ||||||
chr1:230685034 | TA | T | 112 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(109): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1229-47delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230685034 | ||||||
chr1:230685316 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
7 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380+80T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685316 | |||||||
chr1:230685437 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1380+201T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685437 | |||||||
chr1:230685451 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1380+215T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685451 | |||||||
chr1:230685474 | G | T | 2 | a0001c0001t0003g0045 a0001c0001t0004g0280 |
3 | NA18968.hp2 NA19009.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1380+238G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685474 | |||||||
chr1:230685570 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0004g0162 |
2 | HG02055.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1380+334T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685570 | |||||||
chr1:230685656 | G | A | 121 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(118): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1380+420G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685656 | |||||||
chr1:230685738 | T | C | 52 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0044 others(49): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1380+502T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685738 | |||||||
chr1:230685827 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1380+591G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685827 | |||||||
chr1:230685833 | C | T | 1 | a0001c0011t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1380+597C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685833 | |||||||
chr1:230685869 | G | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+633G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685869 | |||||||
chr1:230685900 | G | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+664G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685900 | |||||||
chr1:230686014 | T | C | 112 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(109): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1380+778T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686014 | |||||||
chr1:230686026 | A | G | 3 | a0001c0001t0008g0115 a0001c0001t0008g0118 a0001c0018t0008g0116 |
3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1380+790A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686026 | |||||||
chr1:230686041 | A | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+805A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686041 | |||||||
chr1:230686166 | T | C | 295 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(292): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1381-769T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686166 | |||||||
chr1:230686205 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1381-730G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686205 | |||||||
chr1:230686250 | C | T | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1381-685C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686250 | |||||||
chr1:230686584 | C | T | 121 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(118): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1381-351C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686584 | |||||||
chr1:230686601 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0284 a0001c0001t0001g0291 others(1): Show |
5 | HG02630.hp2 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-334A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686601 | |||||||
chr1:230686725 | C | A | 295 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(292): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1381-210C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686725 | |||||||
chr1:230686733 | G | A | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-202G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686733 | |||||||
chr1:230686812 | T | C | 1 | a0001c0001t0006g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1381-123T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686812 | |||||||
chr1:230686861 | G | A | 174 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(171): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1381-74G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686861 | |||||||
chr1:230686886 | A | C | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1381-49A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686886 | |||||||
chr1:230687157 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0287 a0001c0001t0001g0288 |
5 | HG00140.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+25C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687157 | |||||||
chr1:230687294 | C | T | 174 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(171): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1578+162C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687294 | |||||||
chr1:230687318 | A | G | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1578+186A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687318 | |||||||
chr1:230687342 | T | A | 1 | a0003c0003t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1578+210T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687342 | |||||||
chr1:230687391 | C | T | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0002g0198 |
3 | HG02258.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1578+259C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687391 | |||||||
chr1:230687560 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0284 a0001c0001t0001g0291 others(1): Show |
5 | HG02630.hp2 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+428C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687560 | |||||||
chr1:230687617 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0282 |
5 | HG01069.hp1 HG01175.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-454A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687617 | |||||||
chr1:230687623 | G | A | 1 | a0001c0001t0001g0054 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1579-448G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687623 | |||||||
chr1:230687632 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1579-439T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687632 | |||||||
chr1:230687697 | TC | T | 90 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0021 others(87): Show |
123 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1579-372delC | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 230687697 | ||||||
chr1:230687724 | T | C | 1 | a0003c0003t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1579-347T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687724 | |||||||
chr1:230687738 | T | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0284 a0001c0001t0001g0291 others(1): Show |
5 | HG02630.hp2 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-333T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687738 | |||||||
chr1:230688006 | T | A | 3 | a0001c0001t0008g0115 a0001c0001t0008g0118 a0001c0018t0008g0116 |
3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1579-65T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230688006 | |||||||
chr1:230688047 | A | G | 4 | a0004c0006t0003g0264 a0004c0006t0003g0265 a0004c0006t0003g0268 others(1): Show |
4 | HG01261.hp1 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579-24A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230688047 | |||||||
chr1:230688201 | C | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+58C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 14/17 | chr1 | 230688201 | |||||||
chr1:230688347 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02080.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1652-73G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 14/17 | chr1 | 230688347 | |||||||
chr1:230688643 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1794+81G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688643 | |||||||
chr1:230688835 | G | C | 27 | a0001c0001t0005g0001 a0001c0001t0005g0028 a0001c0001t0005g0031 others(24): Show |
35 | HG00140.hp1 HG00423.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1794+273G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688835 | |||||||
chr1:230688881 | G | A | 168 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(165): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1794+319G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688881 | |||||||
chr1:230688898 | A | C | 1 | a0002c0002t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1794+336A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688898 | |||||||
chr1:230689003 | G | A | 4 | a0004c0006t0003g0264 a0004c0006t0003g0265 a0004c0006t0003g0268 others(1): Show |
4 | HG01261.hp1 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794+441G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689003 | |||||||
chr1:230689015 | G | T | 2 | a0001c0008t0001g0278 a0003c0003t0001g0129 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1794+453G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689015 | |||||||
chr1:230689092 | A | G | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1794+530A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689092 | |||||||
chr1:230689179 | GTTTTTAT others(15): Show |
G | 1 | a0002c0002t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1794+622_1794+643d others(24): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 230689179 | ||||||
chr1:230689187 | TAAAA | T | 63 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0046 others(60): Show |
84 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1794+630_1794+633d others(6): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 230689187 | ||||||
chr1:230689266 | A | G | 121 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(118): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1794+704A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689266 | |||||||
chr1:230689651 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0117 |
3 | HG02258.hp2 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1795-363C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689651 | |||||||
chr1:230689681 | T | G | 92 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0021 others(89): Show |
125 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1795-333T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689681 | |||||||
chr1:230689686 | G | A | 1 | a0009c0023t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-328G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689686 | |||||||
chr1:230689701 | T | C | 121 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0003 others(118): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1795-313T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689701 | |||||||
chr1:230689722 | G | A | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1795-292G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689722 | |||||||
chr1:230689754 | C | T | 46 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0044 others(43): Show |
58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1795-260C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689754 | |||||||
chr1:230689899 | G | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-115G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689899 | |||||||
chr1:230689944 | T | A | 1 | a0001c0011t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1795-70T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689944 | |||||||
chr1:230690196 | A | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1934+43A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690196 | |||||||
chr1:230690236 | A | G | 2 | a0001c0001t0003g0231 a0001c0001t0004g0153 |
2 | NA18985.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1934+83A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690236 | |||||||
chr1:230690429 | C | G | 1 | a0003c0003t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1934+276C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690429 | |||||||
chr1:230690577 | C | T | 1 | a0001c0005t0001g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1934+424C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690577 | |||||||
chr1:230690915 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1935-469G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690915 | |||||||
chr1:230690952 | A | C | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1935-432A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690952 | |||||||
chr1:230691160 | CAT | C | 16 | a0001c0001t0001g0046 a0001c0001t0002g0017 a0001c0001t0002g0019 others(13): Show |
25 | HG00544.hp1 HG00597.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.1935-221_1935-220d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691160 | ||||||
chr1:230691177 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1935-207A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230691177 | |||||||
chr1:230691178 | T | TATATATA others(27): Show |
3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0011t0001g0093 |
3 | HG02080.hp1 HG03139.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1935-199_1935-198i others(36): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691178 | ||||||
chr1:230691189 | G | GTATATAC others(27): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0291 a0001c0001t0001g0296 |
4 | HG02630.hp2 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935-163_1935-162i others(36): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691189 | ||||||
chr1:230691189 | G | GTATATAC others(61): Show |
1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1935-163_1935-162i others(70): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691189 | ||||||
chr1:230691197 | A | G | 1 | a0001c0011t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1935-187A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230691197 | |||||||
chr1:230691250 | T | TA | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0011t0001g0093 |
3 | HG02080.hp1 HG03139.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1935-133dupA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691250 | ||||||
chr1:230691841 | A | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0003c0003t0001g0257 others(1): Show |
7 | HG00741.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2115+277A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230691841 | |||||||
chr1:230691887 | C | T | 3 | a0001c0008t0001g0278 a0003c0003t0001g0129 a0009c0023t0001g0241 |
3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2115+323C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230691887 | |||||||
chr1:230692208 | G | T | 1 | a0001c0001t0004g0166 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2115+644G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692208 | |||||||
chr1:230692227 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2115+663C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692227 | |||||||
chr1:230692231 | G | A | 1 | a0003c0003t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2115+667G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692231 | |||||||
chr1:230692352 | GA | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0284 others(15): Show |
22 | HG01106.hp1 HG01243.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.2115+800delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230692352 | ||||||
chr1:230692486 | A | T | 2 | a0003c0003t0001g0051 a0003c0003t0001g0263 |
3 | HG02615.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2116-806A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692486 | |||||||
chr1:230692553 | G | A | 28 | a0001c0001t0005g0001 a0001c0001t0005g0028 a0001c0001t0005g0031 others(25): Show |
36 | HG00140.hp1 HG00423.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2116-739G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692553 | |||||||
chr1:230692602 | G | T | 200 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0034 others(197): Show |
267 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.2116-690G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692602 | |||||||
chr1:230692613 | T | C | 92 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(89): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2116-679T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692613 | |||||||
chr1:230692641 | G | A | 290 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(287): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.2116-651G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692641 | |||||||
chr1:230692645 | A | G | 147 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(144): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2116-647A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692645 | |||||||
chr1:230692692 | A | G | 140 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0127 others(137): Show |
186 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.2116-600A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692692 | |||||||
chr1:230692727 | CTG | C | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2116-562_2116-561d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230692727 | ||||||
chr1:230692759 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2116-533C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692759 | |||||||
chr1:230692789 | GTTA | G | 154 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(151): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.2116-500_2116-498d others(5): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230692789 | ||||||
chr1:230692792 | A | G | 6 | a0001c0001t0001g0127 a0001c0001t0001g0236 a0001c0001t0009g0042 others(3): Show |
7 | HG01433.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2116-500A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692792 | |||||||
chr1:230692918 | A | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0002g0138 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2116-374A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692918 | |||||||
chr1:230693014 | A | G | 135 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0284 others(132): Show |
180 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.2116-278A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693014 | |||||||
chr1:230693019 | G | T | 292 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(289): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.2116-273G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693019 | |||||||
chr1:230693127 | A | G | 118 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0021 others(115): Show |
159 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.2116-165A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693127 | |||||||
chr1:230693225 | CT | C | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2116-59delT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230693225 | ||||||
chr1:230693227 | T | C | 6 | a0001c0005t0001g0047 a0001c0005t0001g0048 a0001c0005t0001g0243 others(3): Show |
7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2116-65T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693227 | |||||||
chr1:230693233 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0009g0042 |
3 | HG02717.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2116-59T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693233 | |||||||
chr1:230693235 | C | T | 1 | a0001c0001t0009g0042 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2116-57C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693235 | |||||||
chr1:230693241 | C | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2116-51C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693241 | |||||||
chr1:230693279 | A | G | 1 | a0001c0017t0004g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2116-13A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693279 | |||||||
chr1:230693282 | G | A | 1 | a0001c0001t0004g0280 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2116-10G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693282 |